Mee-Len Chye

Mee-Len Chye

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Mee-Len Chye

Mee-Len Chye

Publications by authors named "Mee-Len Chye"

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Polyunsaturated linolenoyl-CoA modulates ERF-VII-mediated hypoxia signaling in Arabidopsis.

J Integr Plant Biol 2019 Oct 8. Epub 2019 Oct 8.

State Key Laboratory of Biocontrol, Guangdong Provincial Key Laboratory of Plant Resources, School of Life Sciences, Sun Yat-Sen University, Guangzhou, 510275, China.

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http://dx.doi.org/10.1111/jipb.12875DOI Listing
October 2019

Overexpression of HMG-CoA synthase promotes Arabidopsis root growth and adversely affects glucosinolate biosynthesis.

J Exp Bot 2019 Sep 26. Epub 2019 Sep 26.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.

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http://dx.doi.org/10.1093/jxb/erz420DOI Listing
September 2019

The overexpression of rice ACYL-CoA-BINDING PROTEIN2 increases grain size and bran oil content in transgenic rice.

Plant J 2019 Aug 22. Epub 2019 Aug 22.

School of Biological Sciences, University of Hong Kong, Pokfulam, Hong Kong, China.

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http://dx.doi.org/10.1111/tpj.14503DOI Listing
August 2019

Arabidopsis acyl-CoA-binding proteins regulate the synthesis of lipid signals.

New Phytol 2019 07 25;223(1):113-117. Epub 2019 Feb 25.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.

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http://dx.doi.org/10.1111/nph.15707DOI Listing
July 2019

Overexpression of a Monocot Acyl-CoA-Binding Protein Confers Broad-Spectrum Pathogen Protection in a Dicot.

Proteomics 2019 Jun;19(12):e1800368

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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https://onlinelibrary.wiley.com/doi/abs/10.1002/pmic.2018003
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http://dx.doi.org/10.1002/pmic.201800368DOI Listing
June 2019

Arabidopsis ACYL-COA-BINDING PROTEIN1 interacts with STEROL C4-METHYL OXIDASE1-2 to modulate gene expression of homeodomain-leucine zipper IV transcription factors.

New Phytol 2018 04 30;218(1):183-200. Epub 2017 Dec 30.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.

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http://dx.doi.org/10.1111/nph.14965DOI Listing
April 2018

Improved fruit α-tocopherol, carotenoid, squalene and phytosterol contents through manipulation of Brassica juncea 3-HYDROXY-3-METHYLGLUTARYL-COA SYNTHASE1 in transgenic tomato.

Plant Biotechnol J 2018 03 17;16(3):784-796. Epub 2017 Oct 17.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.

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http://dx.doi.org/10.1111/pbi.12828DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814594PMC
March 2018

Depletion of Arabidopsis ACYL-COA-BINDING PROTEIN3 Affects Fatty Acid Composition in the Phloem.

Front Plant Sci 2018 25;9. Epub 2018 Jan 25.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong.

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http://dx.doi.org/10.3389/fpls.2018.00002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789640PMC
January 2018

The potential of the mevalonate pathway for enhanced isoprenoid production.

Biotechnol Adv 2016 Sep-Oct;34(5):697-713. Epub 2016 Mar 16.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China. Electronic address:

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http://dx.doi.org/10.1016/j.biotechadv.2016.03.005DOI Listing
December 2017

Arabidopsis thaliana Acyl-CoA-binding protein ACBP6 interacts with plasmodesmata-located protein PDLP8.

Plant Signal Behav 2017 08 8;12(8):e1359365. Epub 2017 Aug 8.

a School of Biological Sciences , The University of Hong Kong , Hong Kong , China.

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http://dx.doi.org/10.1080/15592324.2017.1359365DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5616145PMC
August 2017

Acyl-CoA-Binding Protein ACBP1 Modulates Sterol Synthesis during Embryogenesis.

Plant Physiol 2017 Jul 12;174(3):1420-1435. Epub 2017 May 12.

School of Biological Sciences, University of Hong Kong, Pokfulam, Hong Kong, China

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http://dx.doi.org/10.1104/pp.17.00412DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490911PMC
July 2017

The first plant acyl-CoA-binding protein structures: the close homologues OsACBP1 and OsACBP2 from rice.

Acta Crystallogr D Struct Biol 2017 May 26;73(Pt 5):438-448. Epub 2017 Apr 26.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong.

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http://dx.doi.org/10.1107/S2059798317004193DOI Listing
May 2017

Kelch-motif containing acyl-CoA binding proteins AtACBP4 and AtACBP5 are differentially expressed and function in floral lipid metabolism.

Plant Mol Biol 2017 Jan 8;93(1-2):209-225. Epub 2016 Nov 8.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1007/s11103-016-0557-5DOI Listing
January 2017

Arabidopsis acyl-CoA-binding protein ACBP6 localizes in the phloem and affects jasmonate composition.

Plant Mol Biol 2016 Dec 19;92(6):717-730. Epub 2016 Sep 19.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1007/s11103-016-0541-0DOI Listing
December 2016

Deciphering the roles of acyl-CoA-binding proteins in plant cells.

Protoplasma 2016 Sep 4;253(5):1177-95. Epub 2015 Sep 4.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.

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http://dx.doi.org/10.1007/s00709-015-0882-6DOI Listing
September 2016

The binding versatility of plant acyl-CoA-binding proteins and their significance in lipid metabolism.

Biochim Biophys Acta 2016 09 31;1861(9 Pt B):1409-1421. Epub 2015 Dec 31.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China. Electronic address:

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http://dx.doi.org/10.1016/j.bbalip.2015.12.018DOI Listing
September 2016

Acyl-CoA-Binding Proteins (ACBPs) in Plant Development.

Subcell Biochem 2016 ;86:363-404

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.

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http://dx.doi.org/10.1007/978-3-319-25979-6_15DOI Listing
July 2016

Plant acyl-CoA-binding proteins: An emerging family involved in plant development and stress responses.

Prog Lipid Res 2016 07 29;63:165-81. Epub 2016 Jun 29.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong. Electronic address:

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http://dx.doi.org/10.1016/j.plipres.2016.06.002DOI Listing
July 2016

Characterization of a small acyl-CoA-binding protein (ACBP) from Helianthus annuus L. and its binding affinities.

Plant Physiol Biochem 2016 May 18;102:141-50. Epub 2016 Feb 18.

Instituto de la Grasa (CSIC), Campus Universitario Pablo de Olavide, Ctra. de Utrera Km 1, 41013 Seville, Spain. Electronic address:

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http://dx.doi.org/10.1016/j.plaphy.2016.02.025DOI Listing
May 2016

Plant Cytosolic Acyl-CoA-Binding Proteins.

Lipids 2016 Jan 12;51(1):1-13. Epub 2015 Dec 12.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1007/s11745-015-4103-zDOI Listing
January 2016

Rice acyl-CoA-binding proteins OsACBP4 and OsACBP5 are differentially localized in the endoplasmic reticulum of transgenic Arabidopsis.

Plant Signal Behav 2014 ;9(8):e29544

a School of Biological Sciences; The University of Hong Kong; Pokfulam, Hong Kong, PR China.

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http://dx.doi.org/10.4161/psb.29544DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4205152PMC
October 2015

Gene expression in plant lipid metabolism in Arabidopsis seedlings.

PLoS One 2014 29;9(9):e107372. Epub 2014 Sep 29.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0107372PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180049PMC
June 2015

The Arabidopsis cytosolic Acyl-CoA-binding proteins play combinatory roles in pollen development.

Plant Cell Physiol 2015 Feb 12;56(2):322-33. Epub 2014 Nov 12.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China

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http://dx.doi.org/10.1093/pcp/pcu163DOI Listing
February 2015

Expression of Arabidopsis acyl-CoA-binding proteins AtACBP1 and AtACBP4 confers Pb(II) accumulation in Brassica juncea roots.

Plant Cell Environ 2015 Jan 17;38(1):101-17. Epub 2014 Jul 17.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.

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http://dx.doi.org/10.1111/pce.12382DOI Listing
January 2015

Arabidopsis membrane-associated acyl-CoA-binding protein ACBP1 is involved in stem cuticle formation.

J Exp Bot 2014 Oct 22;65(18):5473-83. Epub 2014 Jul 22.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China

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http://dx.doi.org/10.1093/jxb/eru304DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4157719PMC
October 2014

Past achievements, current status and future perspectives of studies on 3-hydroxy-3-methylglutaryl-CoA synthase (HMGS) in the mevalonate (MVA) pathway.

Plant Cell Rep 2014 Jul 30;33(7):1005-22. Epub 2014 Mar 30.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China,

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http://dx.doi.org/10.1007/s00299-014-1592-9DOI Listing
July 2014

Subcellular localization of rice acyl-CoA-binding proteins (ACBPs) indicates that OsACBP6::GFP is targeted to the peroxisomes.

New Phytol 2014 Jul 16;203(2):469-82. Epub 2014 Apr 16.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China; College of Life Science, Northeast Forestry University, Harbin, China.

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http://dx.doi.org/10.1111/nph.12809DOI Listing
July 2014

Transgenic Arabidopsis flowers overexpressing acyl-CoA-binding protein ACBP6 are freezing tolerant.

Plant Cell Physiol 2014 Jun 19;55(6):1055-71. Epub 2014 Feb 19.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China

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http://dx.doi.org/10.1093/pcp/pcu037DOI Listing
June 2014

Strong seed-specific protein expression from the Vigna radiata storage protein 8SGα promoter in transgenic Arabidopsis seeds.

J Biotechnol 2014 Mar 3;174:49-56. Epub 2014 Feb 3.

College of Life Science and Technology, Jinan University, Guangzhou 510632, China. Electronic address:

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http://dx.doi.org/10.1016/j.jbiotec.2014.01.027DOI Listing
March 2014

Sorghum extracellular leucine-rich repeat protein SbLRR2 mediates lead tolerance in transgenic Arabidopsis.

Plant Cell Physiol 2013 Sep 22;54(9):1549-59. Epub 2013 Jul 22.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1093/pcp/pct101DOI Listing
September 2013

Interactions between Arabidopsis acyl-CoA-binding proteins and their protein partners.

Planta 2013 Aug 7;238(2):239-45. Epub 2013 Jun 7.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.

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http://dx.doi.org/10.1007/s00425-013-1904-2DOI Listing
August 2013

A Vigna radiata 8S globulin α' promoter drives efficient expression of GUS in Arabidopsis cotyledonary embryos.

J Agric Food Chem 2013 Jul 25;61(26):6423-9. Epub 2013 Jun 25.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.

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http://dx.doi.org/10.1021/jf401537qDOI Listing
July 2013

Arabidopsis acyl-CoA-binding protein ACBP1 participates in the regulation of seed germination and seedling development.

Plant J 2013 Apr 1;74(2):294-309. Epub 2013 Mar 1.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.

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http://dx.doi.org/10.1111/tpj.12121DOI Listing
April 2013

Overexpression of Arabidopsis acyl-CoA-binding protein ACBP2 enhances drought tolerance.

Plant Cell Environ 2013 Feb 8;36(2):300-14. Epub 2012 Aug 8.

School of Biological Sciences, The University of Hong Kong, Hong Kong, China.

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http://dx.doi.org/10.1111/j.1365-3040.2012.02574.xDOI Listing
February 2013

The gene encoding Arabidopsis acyl-CoA-binding protein 3 is pathogen inducible and subject to circadian regulation.

J Exp Bot 2012 May 15;63(8):2985-3000. Epub 2012 Feb 15.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1093/jxb/ers009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350915PMC
May 2012

Guidelines for the use and interpretation of assays for monitoring autophagy.

Authors:
Daniel J Klionsky Fabio C Abdalla Hagai Abeliovich Robert T Abraham Abraham Acevedo-Arozena Khosrow Adeli Lotta Agholme Maria Agnello Patrizia Agostinis Julio A Aguirre-Ghiso Hyung Jun Ahn Ouardia Ait-Mohamed Slimane Ait-Si-Ali Takahiko Akematsu Shizuo Akira Hesham M Al-Younes Munir A Al-Zeer Matthew L Albert Roger L Albin Javier Alegre-Abarrategui Maria Francesca Aleo Mehrdad Alirezaei Alexandru Almasan Maylin Almonte-Becerril Atsuo Amano Ravi Amaravadi Shoba Amarnath Amal O Amer Nathalie Andrieu-Abadie Vellareddy Anantharam David K Ann Shailendra Anoopkumar-Dukie Hiroshi Aoki Nadezda Apostolova Giuseppe Arancia John P Aris Katsuhiko Asanuma Nana Y O Asare Hisashi Ashida Valerie Askanas David S Askew Patrick Auberger Misuzu Baba Steven K Backues Eric H Baehrecke Ben A Bahr Xue-Yuan Bai Yannick Bailly Robert Baiocchi Giulia Baldini Walter Balduini Andrea Ballabio Bruce A Bamber Edward T W Bampton Gábor Bánhegyi Clinton R Bartholomew Diane C Bassham Robert C Bast Henri Batoko Boon-Huat Bay Isabelle Beau Daniel M Béchet Thomas J Begley Christian Behl Christian Behrends Soumeya Bekri Bryan Bellaire Linda J Bendall Luca Benetti Laura Berliocchi Henri Bernardi Francesca Bernassola Sébastien Besteiro Ingrid Bhatia-Kissova Xiaoning Bi Martine Biard-Piechaczyk Janice S Blum Lawrence H Boise Paolo Bonaldo David L Boone Beat C Bornhauser Karina R Bortoluci Ioannis Bossis Frédéric Bost Jean-Pierre Bourquin Patricia Boya Michaël Boyer-Guittaut Peter V Bozhkov Nathan R Brady Claudio Brancolini Andreas Brech Jay E Brenman Ana Brennand Emery H Bresnick Patrick Brest Dave Bridges Molly L Bristol Paul S Brookes Eric J Brown John H Brumell Nicola Brunetti-Pierri Ulf T Brunk Dennis E Bulman Scott J Bultman Geert Bultynck Lena F Burbulla Wilfried Bursch Jonathan P Butchar Wanda Buzgariu Sergio P Bydlowski Ken Cadwell Monika Cahová Dongsheng Cai Jiyang Cai Qian Cai Bruno Calabretta Javier Calvo-Garrido Nadine Camougrand Michelangelo Campanella Jenny Campos-Salinas Eleonora Candi Lizhi Cao Allan B Caplan Simon R Carding Sandra M Cardoso Jennifer S Carew Cathleen R Carlin Virginie Carmignac Leticia A M Carneiro Serena Carra Rosario A Caruso Giorgio Casari Caty Casas Roberta Castino Eduardo Cebollero Francesco Cecconi Jean Celli Hassan Chaachouay Han-Jung Chae Chee-Yin Chai David C Chan Edmond Y Chan Raymond Chuen-Chung Chang Chi-Ming Che Ching-Chow Chen Guang-Chao Chen Guo-Qiang Chen Min Chen Quan Chen Steve S-L Chen WenLi Chen Xi Chen Xiangmei Chen Xiequn Chen Ye-Guang Chen Yingyu Chen Yongqiang Chen Yu-Jen Chen Zhixiang Chen Alan Cheng Christopher H K Cheng Yan Cheng Heesun Cheong Jae-Ho Cheong Sara Cherry Russ Chess-Williams Zelda H Cheung Eric Chevet Hui-Ling Chiang Roberto Chiarelli Tomoki Chiba Lih-Shen Chin Shih-Hwa Chiou Francis V Chisari Chi Hin Cho Dong-Hyung Cho Augustine M K Choi DooSeok Choi Kyeong Sook Choi Mary E Choi Salem Chouaib Divaker Choubey Vinay Choubey Charleen T Chu Tsung-Hsien Chuang Sheau-Huei Chueh Taehoon Chun Yong-Joon Chwae Mee-Len Chye Roberto Ciarcia Maria R Ciriolo Michael J Clague Robert S B Clark Peter G H Clarke Robert Clarke Patrice Codogno Hilary A Coller María I Colombo Sergio Comincini Maria Condello Fabrizio Condorelli Mark R Cookson Graham H Coombs Isabelle Coppens Ramon Corbalan Pascale Cossart Paola Costelli Safia Costes Ana Coto-Montes Eduardo Couve Fraser P Coxon James M Cregg José L Crespo Marianne J Cronjé Ana Maria Cuervo Joseph J Cullen Mark J Czaja Marcello D'Amelio Arlette Darfeuille-Michaud Lester M Davids Faith E Davies Massimo De Felici John F de Groot Cornelis A M de Haan Luisa De Martino Angelo De Milito Vincenzo De Tata Jayanta Debnath Alexei Degterev Benjamin Dehay Lea M D Delbridge Francesca Demarchi Yi Zhen Deng Jörn Dengjel Paul Dent Donna Denton Vojo Deretic Shyamal D Desai Rodney J Devenish Mario Di Gioacchino Gilbert Di Paolo Chiara Di Pietro Guillermo Díaz-Araya Inés Díaz-Laviada Maria T Diaz-Meco Javier Diaz-Nido Ivan Dikic Savithramma P Dinesh-Kumar Wen-Xing Ding Clark W Distelhorst Abhinav Diwan Mojgan Djavaheri-Mergny Svetlana Dokudovskaya Zheng Dong Frank C Dorsey Victor Dosenko James J Dowling Stephen Doxsey Marlène Dreux Mark E Drew Qiuhong Duan Michel A Duchosal Karen Duff Isabelle Dugail Madeleine Durbeej Michael Duszenko Charles L Edelstein Aimee L Edinger Gustavo Egea Ludwig Eichinger N Tony Eissa Suhendan Ekmekcioglu Wafik S El-Deiry Zvulun Elazar Mohamed Elgendy Lisa M Ellerby Kai Er Eng Anna-Mart Engelbrecht Simone Engelender Jekaterina Erenpreisa Ricardo Escalante Audrey Esclatine Eeva-Liisa Eskelinen Lucile Espert Virginia Espina Huizhou Fan Jia Fan Qi-Wen Fan Zhen Fan Shengyun Fang Yongqi Fang Manolis Fanto Alessandro Fanzani Thomas Farkas Jean-Claude Farré Mathias Faure Marcus Fechheimer Carl G Feng Jian Feng Qili Feng Youji Feng László Fésüs Ralph Feuer Maria E Figueiredo-Pereira Gian Maria Fimia Diane C Fingar Steven Finkbeiner Toren Finkel Kim D Finley Filomena Fiorito Edward A Fisher Paul B Fisher Marc Flajolet Maria L Florez-McClure Salvatore Florio Edward A Fon Francesco Fornai Franco Fortunato Rati Fotedar Daniel H Fowler Howard S Fox Rodrigo Franco Lisa B Frankel Marc Fransen José M Fuentes Juan Fueyo Jun Fujii Kozo Fujisaki Eriko Fujita Mitsunori Fukuda Ruth H Furukawa Matthias Gaestel Philippe Gailly Malgorzata Gajewska Brigitte Galliot Vincent Galy Subramaniam Ganesh Barry Ganetzky Ian G Ganley Fen-Biao Gao George F Gao Jinming Gao Lorena Garcia Guillermo Garcia-Manero Mikel Garcia-Marcos Marjan Garmyn Andrei L Gartel Evelina Gatti Mathias Gautel Thomas R Gawriluk Matthew E Gegg Jiefei Geng Marc Germain Jason E Gestwicki David A Gewirtz Saeid Ghavami Pradipta Ghosh Anna M Giammarioli Alexandra N Giatromanolaki Spencer B Gibson Robert W Gilkerson Michael L Ginger Henry N Ginsberg Jakub Golab Michael S Goligorsky Pierre Golstein Candelaria Gomez-Manzano Ebru Goncu Céline Gongora Claudio D Gonzalez Ramon Gonzalez Cristina González-Estévez Rosa Ana González-Polo Elena Gonzalez-Rey Nikolai V Gorbunov Sharon Gorski Sandro Goruppi Roberta A Gottlieb Devrim Gozuacik Giovanna Elvira Granato Gary D Grant Kim N Green Aleš Gregorc Frédéric Gros Charles Grose Thomas W Grunt Philippe Gual Jun-Lin Guan Kun-Liang Guan Sylvie M Guichard Anna S Gukovskaya Ilya Gukovsky Jan Gunst Asa B Gustafsson Andrew J Halayko Amber N Hale Sandra K Halonen Maho Hamasaki Feng Han Ting Han Michael K Hancock Malene Hansen Hisashi Harada Masaru Harada Stefan E Hardt J Wade Harper Adrian L Harris James Harris Steven D Harris Makoto Hashimoto Jeffrey A Haspel Shin-ichiro Hayashi Lori A Hazelhurst Congcong He You-Wen He Marie-Joseé Hébert Kim A Heidenreich Miep H Helfrich Gudmundur V Helgason Elizabeth P Henske Brian Herman Paul K Herman Claudio Hetz Sabine Hilfiker Joseph A Hill Lynne J Hocking Paul Hofman Thomas G Hofmann Jörg Höhfeld Tessa L Holyoake Ming-Huang Hong David A Hood Gökhan S Hotamisligil Ewout J Houwerzijl Maria Høyer-Hansen Bingren Hu Chien-An A Hu Hong-Ming Hu Ya Hua Canhua Huang Ju Huang Shengbing Huang Wei-Pang Huang Tobias B Huber Won-Ki Huh Tai-Ho Hung Ted R Hupp Gang Min Hur James B Hurley Sabah N A Hussain Patrick J Hussey Jung Jin Hwang Seungmin Hwang Atsuhiro Ichihara Shirin Ilkhanizadeh Ken Inoki Takeshi Into Valentina Iovane Juan L Iovanna Nancy Y Ip Yoshitaka Isaka Hiroyuki Ishida Ciro Isidoro Ken-ichi Isobe Akiko Iwasaki Marta Izquierdo Yotaro Izumi Panu M Jaakkola Marja Jäättelä George R Jackson William T Jackson Bassam Janji Marina Jendrach Ju-Hong Jeon Eui-Bae Jeung Hong Jiang Hongchi Jiang Jean X Jiang Ming Jiang Qing Jiang Xuejun Jiang Xuejun Jiang Alberto Jiménez Meiyan Jin Shengkan Jin Cheol O Joe Terje Johansen Daniel E Johnson Gail V W Johnson Nicola L Jones Bertrand Joseph Suresh K Joseph Annie M Joubert Gábor Juhász Lucienne Juillerat-Jeanneret Chang Hwa Jung Yong-Keun Jung Kai Kaarniranta Allen Kaasik Tomohiro Kabuta Motoni Kadowaki Katarina Kagedal Yoshiaki Kamada Vitaliy O Kaminskyy Harm H Kampinga Hiromitsu Kanamori Chanhee Kang Khong Bee Kang Kwang Il Kang Rui Kang Yoon-A Kang Tomotake Kanki Thirumala-Devi Kanneganti Haruo Kanno Anumantha G Kanthasamy Arthi Kanthasamy Vassiliki Karantza Gur P Kaushal Susmita Kaushik Yoshinori Kawazoe Po-Yuan Ke John H Kehrl Ameeta Kelekar Claus Kerkhoff David H Kessel Hany Khalil Jan A K W Kiel Amy A Kiger Akio Kihara Deok Ryong Kim Do-Hyung Kim Dong-Hou Kim Eun-Kyoung Kim Hyung-Ryong Kim Jae-Sung Kim Jeong Hun Kim Jin Cheon Kim John K Kim Peter K Kim Seong Who Kim Yong-Sun Kim Yonghyun Kim Adi Kimchi Alec C Kimmelman Jason S King Timothy J Kinsella Vladimir Kirkin Lorrie A Kirshenbaum Katsuhiko Kitamoto Kaio Kitazato Ludger Klein Walter T Klimecki Jochen Klucken Erwin Knecht Ben C B Ko Jan C Koch Hiroshi Koga Jae-Young Koh Young Ho Koh Masato Koike Masaaki Komatsu Eiki Kominami Hee Jeong Kong Wei-Jia Kong Viktor I Korolchuk Yaichiro Kotake Michael I Koukourakis Juan B Kouri Flores Attila L Kovács Claudine Kraft Dimitri Krainc Helmut Krämer Carole Kretz-Remy Anna M Krichevsky Guido Kroemer Rejko Krüger Oleg Krut Nicholas T Ktistakis Chia-Yi Kuan Roza Kucharczyk Ashok Kumar Raj Kumar Sharad Kumar Mondira Kundu Hsing-Jien Kung Tino Kurz Ho Jeong Kwon Albert R La Spada Frank Lafont Trond Lamark Jacques Landry Jon D Lane Pierre Lapaquette Jocelyn F Laporte Lajos László Sergio Lavandero Josée N Lavoie Robert Layfield Pedro A Lazo Weidong Le Laurent Le Cam Daniel J Ledbetter Alvin J X Lee Byung-Wan Lee Gyun Min Lee Jongdae Lee Ju-Hyun Lee Michael Lee Myung-Shik Lee Sug Hyung Lee Christiaan Leeuwenburgh Patrick Legembre Renaud Legouis Michael Lehmann Huan-Yao Lei Qun-Ying Lei David A Leib José Leiro John J Lemasters Antoinette Lemoine Maciej S Lesniak Dina Lev Victor V Levenson Beth Levine Efrat Levy Faqiang Li Jun-Lin Li Lian Li Sheng Li Weijie Li Xue-Jun Li Yan-bo Li Yi-Ping Li Chengyu Liang Qiangrong Liang Yung-Feng Liao Pawel P Liberski Andrew Lieberman Hyunjung J Lim Kah-Leong Lim Kyu Lim Chiou-Feng Lin Fu-Cheng Lin Jian Lin Jiandie D Lin Kui Lin Wan-Wan Lin Weei-Chin Lin Yi-Ling Lin Rafael Linden Paul Lingor Jennifer Lippincott-Schwartz Michael P Lisanti Paloma B Liton Bo Liu Chun-Feng Liu Kaiyu Liu Leyuan Liu Qiong A Liu Wei Liu Young-Chau Liu Yule Liu Richard A Lockshin Chun-Nam Lok Sagar Lonial Benjamin Loos Gabriel Lopez-Berestein Carlos López-Otín Laura Lossi Michael T Lotze Peter Lőw Binfeng Lu Bingwei Lu Bo Lu Zhen Lu Frédéric Luciano Nicholas W Lukacs Anders H Lund Melinda A Lynch-Day Yong Ma Fernando Macian Jeff P MacKeigan Kay F Macleod Frank Madeo Luigi Maiuri Maria Chiara Maiuri Davide Malagoli May Christine V Malicdan Walter Malorni Na Man Eva-Maria Mandelkow Stéphen Manon Irena Manov Kai Mao Xiang Mao Zixu Mao Philippe Marambaud Daniela Marazziti Yves L Marcel Katie Marchbank Piero Marchetti Stefan J Marciniak Mateus Marcondes Mohsen Mardi Gabriella Marfe Guillermo Mariño Maria Markaki Mark R Marten Seamus J Martin Camille Martinand-Mari Wim Martinet Marta Martinez-Vicente Matilde Masini Paola Matarrese Saburo Matsuo Raffaele Matteoni Andreas Mayer Nathalie M Mazure David J McConkey Melanie J McConnell Catherine McDermott Christine McDonald Gerald M McInerney Sharon L McKenna BethAnn McLaughlin Pamela J McLean Christopher R McMaster G Angus McQuibban Alfred J Meijer Miriam H Meisler Alicia Meléndez Thomas J Melia Gerry Melino Maria A Mena Javier A Menendez Rubem F S Menna-Barreto Manoj B Menon Fiona M Menzies Carol A Mercer Adalberto Merighi Diane E Merry Stefania Meschini Christian G Meyer Thomas F Meyer Chao-Yu Miao Jun-Ying Miao Paul A M Michels Carine Michiels Dalibor Mijaljica Ana Milojkovic Saverio Minucci Clelia Miracco Cindy K Miranti Ioannis Mitroulis Keisuke Miyazawa Noboru Mizushima Baharia Mograbi Simin Mohseni Xavier Molero Bertrand Mollereau Faustino Mollinedo Takashi Momoi Iryna Monastyrska Martha M Monick Mervyn J Monteiro Michael N Moore Rodrigo Mora Kevin Moreau Paula I Moreira Yuji Moriyasu Jorge Moscat Serge Mostowy Jeremy C Mottram Tomasz Motyl Charbel E-H Moussa Sylke Müller Sylviane Muller Karl Münger Christian Münz Leon O Murphy Maureen E Murphy Antonio Musarò Indira Mysorekar Eiichiro Nagata Kazuhiro Nagata Aimable Nahimana Usha Nair Toshiyuki Nakagawa Kiichi Nakahira Hiroyasu Nakano Hitoshi Nakatogawa Meera Nanjundan Naweed I Naqvi Derek P Narendra Masashi Narita Miguel Navarro Steffan T Nawrocki Taras Y Nazarko Andriy Nemchenko Mihai G Netea Thomas P Neufeld Paul A Ney Ioannis P Nezis Huu Phuc Nguyen Daotai Nie Ichizo Nishino Corey Nislow Ralph A Nixon Takeshi Noda Angelika A Noegel Anna Nogalska Satoru Noguchi Lucia Notterpek Ivana Novak Tomoyoshi Nozaki Nobuyuki Nukina Thorsten Nürnberger Beat Nyfeler Keisuke Obara Terry D Oberley Salvatore Oddo Michinaga Ogawa Toya Ohashi Koji Okamoto Nancy L Oleinick F Javier Oliver Laura J Olsen Stefan Olsson Onya Opota Timothy F Osborne Gary K Ostrander Kinya Otsu Jing-hsiung James Ou Mireille Ouimet Michael Overholtzer Bulent Ozpolat Paolo Paganetti Ugo Pagnini Nicolas Pallet Glen E Palmer Camilla Palumbo Tianhong Pan Theocharis Panaretakis Udai Bhan Pandey Zuzana Papackova Issidora Papassideri Irmgard Paris Junsoo Park Ohkmae K Park Jan B Parys Katherine R Parzych Susann Patschan Cam Patterson Sophie Pattingre John M Pawelek Jianxin Peng David H Perlmutter Ida Perrotta George Perry Shazib Pervaiz Matthias Peter Godefridus J Peters Morten Petersen Goran Petrovski James M Phang Mauro Piacentini Philippe Pierre Valérie Pierrefite-Carle Gérard Pierron Ronit Pinkas-Kramarski Antonio Piras Natik Piri Leonidas C Platanias Stefanie Pöggeler Marc Poirot Angelo Poletti Christian Poüs Mercedes Pozuelo-Rubio Mette Prætorius-Ibba Anil Prasad Mark Prescott Muriel Priault Nathalie Produit-Zengaffinen Ann Progulske-Fox Tassula Proikas-Cezanne Serge Przedborski Karin Przyklenk Rosa Puertollano Julien Puyal Shu-Bing Qian Liang Qin Zheng-Hong Qin Susan E Quaggin Nina Raben Hannah Rabinowich Simon W Rabkin Irfan Rahman Abdelhaq Rami Georg Ramm Glenn Randall Felix Randow V Ashutosh Rao Jeffrey C Rathmell Brinda Ravikumar Swapan K Ray Bruce H Reed John C Reed Fulvio Reggiori Anne Régnier-Vigouroux Andreas S Reichert John J Reiners Russel J Reiter Jun Ren José L Revuelta Christopher J Rhodes Konstantinos Ritis Elizete Rizzo Jeffrey Robbins Michel Roberge Hernan Roca Maria C Roccheri Stephane Rocchi H Peter Rodemann Santiago Rodríguez de Córdoba Bärbel Rohrer Igor B Roninson Kirill Rosen Magdalena M Rost-Roszkowska Mustapha Rouis Kasper M A Rouschop Francesca Rovetta Brian P Rubin David C Rubinsztein Klaus Ruckdeschel Edmund B Rucker Assaf Rudich Emil Rudolf Nelson Ruiz-Opazo Rossella Russo Tor Erik Rusten Kevin M Ryan Stefan W Ryter David M Sabatini Junichi Sadoshima Tapas Saha Tatsuya Saitoh Hiroshi Sakagami Yasuyoshi Sakai Ghasem Hoseini Salekdeh Paolo Salomoni Paul M Salvaterra Guy Salvesen Rosa Salvioli Anthony M J Sanchez José A Sánchez-Alcázar Ricardo Sánchez-Prieto Marco Sandri Uma Sankar Poonam Sansanwal Laura Santambrogio Shweta Saran Sovan Sarkar Minnie Sarwal Chihiro Sasakawa Ausra Sasnauskiene Miklós Sass Ken Sato Miyuki Sato Anthony H V Schapira Michael Scharl Hermann M Schätzl Wiep Scheper Stefano Schiaffino Claudio Schneider Marion E Schneider Regine Schneider-Stock Patricia V Schoenlein Daniel F Schorderet Christoph Schüller Gary K Schwartz Luca Scorrano Linda Sealy Per O Seglen Juan Segura-Aguilar Iban Seiliez Oleksandr Seleverstov Christian Sell Jong Bok Seo Duska Separovic Vijayasaradhi Setaluri Takao Setoguchi Carmine Settembre John J Shacka Mala Shanmugam Irving M Shapiro Eitan Shaulian Reuben J Shaw James H Shelhamer Han-Ming Shen Wei-Chiang Shen Zu-Hang Sheng Yang Shi Kenichi Shibuya Yoshihiro Shidoji Jeng-Jer Shieh Chwen-Ming Shih Yohta Shimada Shigeomi Shimizu Takahiro Shintani Orian S Shirihai Gordon C Shore Andriy A Sibirny Stan B Sidhu Beata Sikorska Elaine C M Silva-Zacarin Alison Simmons Anna Katharina Simon Hans-Uwe Simon Cristiano Simone Anne Simonsen David A Sinclair Rajat Singh Debasish Sinha Frank A Sinicrope Agnieszka Sirko Parco M Siu Efthimios Sivridis Vojtech Skop Vladimir P Skulachev Ruth S Slack Soraya S Smaili Duncan R Smith Maria S Soengas Thierry Soldati Xueqin Song Anil K Sood Tuck Wah Soong Federica Sotgia Stephen A Spector Claudia D Spies Wolfdieter Springer Srinivasa M Srinivasula Leonidas Stefanis Joan S Steffan Ruediger Stendel Harald Stenmark Anastasis Stephanou Stephan T Stern Cinthya Sternberg Björn Stork Peter Strålfors Carlos S Subauste Xinbing Sui David Sulzer Jiaren Sun Shi-Yong Sun Zhi-Jun Sun Joseph J Y Sung Kuninori Suzuki Toshihiko Suzuki Michele S Swanson Charles Swanton Sean T Sweeney Lai-King Sy Gyorgy Szabadkai Ira Tabas Heinrich Taegtmeyer Marco Tafani Krisztina Takács-Vellai Yoshitaka Takano Kaoru Takegawa Genzou Takemura Fumihiko Takeshita Nicholas J Talbot Kevin S W Tan Keiji Tanaka Kozo Tanaka Daolin Tang Dingzhong Tang Isei Tanida Bakhos A Tannous Nektarios Tavernarakis Graham S Taylor Gregory A Taylor J Paul Taylor Lance S Terada Alexei Terman Gianluca Tettamanti Karin Thevissen Craig B Thompson Andrew Thorburn Michael Thumm FengFeng Tian Yuan Tian Glauco Tocchini-Valentini Aviva M Tolkovsky Yasuhiko Tomino Lars Tönges Sharon A Tooze Cathy Tournier John Tower Roberto Towns Vladimir Trajkovic Leonardo H Travassos Ting-Fen Tsai Mario P Tschan Takeshi Tsubata Allan Tsung Boris Turk Lorianne S Turner Suresh C Tyagi Yasuo Uchiyama Takashi Ueno Midori Umekawa Rika Umemiya-Shirafuji Vivek K Unni Maria I Vaccaro Enza Maria Valente Greet Van den Berghe Ida J van der Klei Wouter van Doorn Linda F van Dyk Marjolein van Egmond Leo A van Grunsven Peter Vandenabeele Wim P Vandenberghe Ilse Vanhorebeek Eva C Vaquero Guillermo Velasco Tibor Vellai Jose Miguel Vicencio Richard D Vierstra Miquel Vila Cécile Vindis Giampietro Viola Maria Teresa Viscomi Olga V Voitsekhovskaja Clarissa von Haefen Marcela Votruba Keiji Wada Richard Wade-Martins Cheryl L Walker Craig M Walsh Jochen Walter Xiang-Bo Wan Aimin Wang Chenguang Wang Dawei Wang Fan Wang Fen Wang Guanghui Wang Haichao Wang Hong-Gang Wang Horng-Dar Wang Jin Wang Ke Wang Mei Wang Richard C Wang Xinglong Wang Xuejun Wang Ying-Jan Wang Yipeng Wang Zhen Wang Zhigang Charles Wang Zhinong Wang Derick G Wansink Diane M Ward Hirotaka Watada Sarah L Waters Paul Webster Lixin Wei Conrad C Weihl William A Weiss Scott M Welford Long-Ping Wen Caroline A Whitehouse J Lindsay Whitton Alexander J Whitworth Tom Wileman John W Wiley Simon Wilkinson Dieter Willbold Roger L Williams Peter R Williamson Bradly G Wouters Chenghan Wu Dao-Cheng Wu William K K Wu Andreas Wyttenbach Ramnik J Xavier Zhijun Xi Pu Xia Gengfu Xiao Zhiping Xie Zhonglin Xie Da-zhi Xu Jianzhen Xu Liang Xu Xiaolei Xu Ai Yamamoto Akitsugu Yamamoto Shunhei Yamashina Michiaki Yamashita Xianghua Yan Mitsuhiro Yanagida Dun-Sheng Yang Elizabeth Yang Jin-Ming Yang Shi Yu Yang Wannian Yang Wei Yuan Yang Zhifen Yang Meng-Chao Yao Tso-Pang Yao Behzad Yeganeh Wei-Lien Yen Jia-jing Yin Xiao-Ming Yin Ook-Joon Yoo Gyesoon Yoon Seung-Yong Yoon Tomohiro Yorimitsu Yuko Yoshikawa Tamotsu Yoshimori Kohki Yoshimoto Ho Jin You Richard J Youle Anas Younes Li Yu Long Yu Seong-Woon Yu Wai Haung Yu Zhi-Min Yuan Zhenyu Yue Cheol-Heui Yun Michisuke Yuzaki Olga Zabirnyk Elaine Silva-Zacarin David Zacks Eldad Zacksenhaus Nadia Zaffaroni Zahra Zakeri Herbert J Zeh Scott O Zeitlin Hong Zhang Hui-Ling Zhang Jianhua Zhang Jing-Pu Zhang Lin Zhang Long Zhang Ming-Yong Zhang Xu Dong Zhang Mantong Zhao Yi-Fang Zhao Ying Zhao Zhizhuang J Zhao Xiaoxiang Zheng Boris Zhivotovsky Qing Zhong Cong-Zhao Zhou Changlian Zhu Wei-Guo Zhu Xiao-Feng Zhu Xiongwei Zhu Yuangang Zhu Teresa Zoladek Wei-Xing Zong Antonio Zorzano Jürgen Zschocke Brian Zuckerbraun

Autophagy 2012 Apr;8(4):445-544

Life Sciences Institute, University of Michigan, Ann Arbor, MI, USA.

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http://dx.doi.org/10.4161/auto.19496DOI Listing
April 2012

Overexpression of Arabidopsis ACBP3 enhances NPR1-dependent plant resistance to Pseudomonas syringe pv tomato DC3000.

Plant Physiol 2011 Aug 13;156(4):2069-81. Epub 2011 Jun 13.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.

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August 2011

New roles for acyl-CoA-binding proteins (ACBPs) in plant development, stress responses and lipid metabolism.

Prog Lipid Res 2011 Apr 7;50(2):141-51. Epub 2010 Dec 7.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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April 2011

The rice acyl-CoA-binding protein gene family: phylogeny, expression and functional analysis.

New Phytol 2011 Mar 3;189(4):1170-84. Epub 2010 Dec 3.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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March 2011

The Arabidopsis thaliana ACBP3 regulates leaf senescence by modulating phospholipid metabolism and ATG8 stability.

Autophagy 2010 Aug 2;6(6):802-4. Epub 2010 Aug 2.

School of Biological Sciences, University of Hong Kong, Pokfulam, Hong Kong, China.

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http://dx.doi.org/10.1105/tpc.110.075333DOI Listing
August 2010

Protein interactors of acyl-CoA-binding protein ACBP2 mediate cadmium tolerance in Arabidopsis.

Plant Signal Behav 2010 Aug 1;5(8):1025-7. Epub 2010 Aug 1.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.4161/psb.5.8.12294DOI Listing
August 2010

Acyl-CoA-binding protein 2 binds lysophospholipase 2 and lysoPC to promote tolerance to cadmium-induced oxidative stress in transgenic Arabidopsis.

Plant J 2010 Jun 19;62(6):989-1003. Epub 2010 Mar 19.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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June 2010

The Arabidopsis acbp1acbp2 double mutant lacking acyl-CoA-binding proteins ACBP1 and ACBP2 is embryo lethal.

New Phytol 2010 Jun 22;186(4):843-55. Epub 2010 Mar 22.

School of Biological Sciences, The University of Hong Kong, Hong Kong, China.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4169659PMC
June 2010

Arabidopsis acyl-CoA-binding proteins ACBP1 and ACBP2 show different roles in freezing stress.

Plant Signal Behav 2010 May 20;5(5):607-9. Epub 2010 Apr 20.

School of Biological Sciences; The University of Hong Kong; Hong Kong, China.

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May 2010

Depletion of the membrane-associated acyl-coenzyme A-binding protein ACBP1 enhances the ability of cold acclimation in Arabidopsis.

Plant Physiol 2010 Mar 27;152(3):1585-97. Epub 2010 Jan 27.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2832255PMC
March 2010

Expression of ACBP4 and ACBP5 proteins is modulated by light in Arabidopsis.

Plant Signal Behav 2009 Nov 3;4(11):1063-5. Epub 2009 Nov 3.

School of Biological Sciences, The University of Hong Kong, Hong Kong, China.

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http://dx.doi.org/10.4161/psb.4.11.9718DOI Listing
November 2009

Light-regulated Arabidopsis ACBP4 and ACBP5 encode cytosolic acyl-CoA-binding proteins that bind phosphatidylcholine and oleoyl-CoA ester.

Plant Physiol Biochem 2009 Oct 21;47(10):926-33. Epub 2009 Jun 21.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1016/j.plaphy.2009.06.007DOI Listing
October 2009

The first crystal structures of a family 19 class IV chitinase: the enzyme from Norway spruce.

Plant Mol Biol 2009 Oct 23;71(3):277-89. Epub 2009 Jul 23.

Department of Molecular Biology, Biomedical Center, Swedish University of Agricultural Sciences, 751 24 Uppsala, Sweden.

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October 2009

An Arabidopsis family of six acyl-CoA-binding proteins has three cytosolic members.

Plant Physiol Biochem 2009 Jun 16;47(6):479-84. Epub 2008 Dec 16.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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June 2009

Use of GFP to investigate expression of plant-derived vaccines.

Methods Mol Biol 2009 ;515:275-85

Department of Botany, The University of Hong Kong, Hong Kong, China.

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May 2009

Arabidopsis thaliana acyl-CoA-binding protein ACBP2 interacts with heavy-metal-binding farnesylated protein AtFP6.

New Phytol 2009 23;181(1):89-102. Epub 2008 Sep 23.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China;Department of Anatomy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam Road, Hong Kong, China;State (China) Key Laboratory of Agrobiotechnology, Chinese University of Hong Kong, Shatin, Hong Kong, China.

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February 2009

Arabidopsis acyl-CoA-binding proteins ACBP4 and ACBP5 are subcellularly localized to the cytosol and ACBP4 depletion affects membrane lipid composition.

Plant Mol Biol 2008 Dec 5;68(6):571-83. Epub 2008 Sep 5.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166440PMC
December 2008

Ethylene- and pathogen-inducible Arabidopsis acyl-CoA-binding protein 4 interacts with an ethylene-responsive element binding protein.

J Exp Bot 2008 3;59(14):3997-4006. Epub 2008 Oct 3.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2576630PMC
December 2008

A Brassica juncea chitinase with two-chitin binding domains show anti-microbial properties against phytopathogens and Gram-negative bacteria.

Authors:
Y Guan Mee-Len Chye

Plant Signal Behav 2008 Dec;3(12):1103-5

School of Biological Sciences; The University of Hong Kong; Pokfulam;Hong Kong China.

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http://dx.doi.org/10.4161/psb.3.12.7006DOI Listing
December 2008

Arabidopsis ACBP6 is an acyl-CoA-binding protein associated with phospholipid metabolism.

Plant Signal Behav 2008 Nov;3(11):1019-20

School of Biological Sciences; The University of Hong Kong; Hong Kong China.

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http://dx.doi.org/10.4161/psb.6762DOI Listing
November 2008

Brassica juncea chitinase BjCHI1 inhibits growth of fungal phytopathogens and agglutinates Gram-negative bacteria.

J Exp Bot 2008 31;59(12):3475-84. Epub 2008 Jul 31.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2529242PMC
October 2008

Overexpression of the Arabidopsis 10-kilodalton acyl-coenzyme A-binding protein ACBP6 enhances freezing tolerance.

Plant Physiol 2008 Sep 11;148(1):304-15. Epub 2008 Jul 11.

School of Biological Sciences, University of Hong Kong, Pokfulam, Hong Kong, China.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2528132PMC
September 2008

Arabidopsis ACBP1 overexpressors are Pb(II)-tolerant and accumulate Pb(II).

Plant Signal Behav 2008 Sep;3(9):693-4

School of Biological Sciences; The University of Hong Kong; Hong Kong, China.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2634561PMC
http://dx.doi.org/10.4161/psb.3.9.5845DOI Listing
September 2008

Overexpression of membrane-associated acyl-CoA-binding protein ACBP1 enhances lead tolerance in Arabidopsis.

Plant J 2008 Apr 7;54(1):141-51. Epub 2008 Jan 7.

School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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April 2008

Crystal structures of a family 19 chitinase from Brassica juncea show flexibility of binding cleft loops.

FEBS J 2007 Jul 2;274(14):3695-3703. Epub 2007 Jul 2.

 Department of Molecular Biology, Swedish University of Agricultural Sciences, Uppsala, Sweden Department of Botany, The University of Hong Kong, Pokfulam, Hong Kong Department of Cell and Molecular Biology, Uppsala University, Sweden.

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http://doi.wiley.com/10.1111/j.1742-4658.2007.05906.x
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July 2007

Plant lipidomics: discerning biological function by profiling plant complex lipids using mass spectrometry.

Front Biosci 2007 Jan 1;12:2494-506. Epub 2007 Jan 1.

Kansas Lipidomics Research Center, Division of Biology, Kansas State University, Manhattan, KS 66506, USA.

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http://dx.doi.org/10.2741/2250DOI Listing
January 2007

Accumulation of recombinant SARS-CoV spike protein in plant cytosol and chloroplasts indicate potential for development of plant-derived oral vaccines.

Exp Biol Med (Maywood) 2006 Sep;231(8):1346-52

Department of Botany, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1177/153537020623100808DOI Listing
September 2006

Expression of viral capsid protein antigen against Epstein-Barr virus in plastids of Nicotiana tabacum cv. SR1.

Biotechnol Bioeng 2006 Aug;94(6):1129-37

Department of Botany, University of Hong Kong, Pokfulam Road, Hong Kong SAR, China.

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http://doi.wiley.com/10.1002/bit.20948
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August 2006

Structural basis for the design of potent and species-specific inhibitors of 3-hydroxy-3-methylglutaryl CoA synthases.

Proc Natl Acad Sci U S A 2006 Aug 24;103(31):11491-6. Epub 2006 Jul 24.

Howard Hughes Medical Institute, The Jack H. Skirball Center for Chemical Biology and Proteomics, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.

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http://dx.doi.org/10.1073/pnas.0604935103DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1544197PMC
August 2006

Arabidopsis ACBP3 is an extracellularly targeted acyl-CoA-binding protein.

Planta 2006 Apr 18;223(5):871-81. Epub 2005 Oct 18.

Department of Botany, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1007/s00425-005-0139-2DOI Listing
April 2006

Downregulation of Solanum americanum genes encoding proteinase inhibitor II causes defective seed development.

Plant J 2006 Jan;45(1):58-70

Department of Botany, University of Hong Kong, Pokfulam Road, China.

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January 2006

Brassica juncea HMG-CoA synthase: localization of mRNA and protein.

Planta 2005 Aug 16;221(6):844-56. Epub 2005 Mar 16.

Department of Botany, The University of Hong Kong, Pokfulam, Hong Kong, China.

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http://dx.doi.org/10.1007/s00425-005-1497-5DOI Listing
August 2005

An agglutinating chitinase with two chitin-binding domains confers fungal protection in transgenic potato.

Planta 2005 Mar 13;220(5):717-30. Epub 2004 Oct 13.

Department of Botany, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1007/s00425-004-1391-6DOI Listing
March 2005

Transgenic plant-derived siRNAs can suppress propagation of influenza virus in mammalian cells.

FEBS Lett 2004 Nov;577(3):345-50

Department of Botany, University of Hong Kong, Pokfulam Road, Hong Kong Special Administrative Region, PR China.

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http://dx.doi.org/10.1016/j.febslet.2004.10.027DOI Listing
November 2004

Expression of proteinase inhibitor II proteins during floral development in Solanum americanum.

Planta 2004 Oct 10;219(6):1010-22. Epub 2004 Jun 10.

Department of Botany, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://link.springer.com/10.1007/s00425-004-1306-6
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October 2004

Functional analyses of the chitin-binding domains and the catalytic domain of Brassica juncea chitinase BjCHI1.

Plant Mol Biol 2004 Sep;56(2):285-98

Department of Botany, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1007/s11103-004-3382-1DOI Listing
September 2004

ACBP4 and ACBP5, novel Arabidopsis acyl-CoA-binding proteins with kelch motifs that bind oleoyl-CoA.

Plant Mol Biol 2004 May;55(2):297-309

Department of Botany, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1007/s11103-004-0642-zDOI Listing
May 2004

Inhibition of endogenous trypsin- and chymotrypsin-like activities in transgenic lettuce expressing heterogeneous proteinase inhibitor SaPIN2a.

Planta 2004 Feb 23;218(4):623-9. Epub 2003 Oct 23.

Department of Botany, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1007/s00425-003-1138-9DOI Listing
February 2004

Arabidopsis Acyl-CoA-binding protein ACBP2 interacts with an ethylene-responsive element-binding protein, AtEBP, via its ankyrin repeats.

Plant Mol Biol 2004 Jan;54(2):233-43

Department of Botany, University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1023/B:PLAN.0000028790.75090.abDOI Listing
January 2004

Membrane localization of Arabidopsis acyl-CoA binding protein ACBP2.

Plant Mol Biol 2003 Mar;51(4):483-92

Department of Botany, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1023/a:1022330304402DOI Listing
March 2003

Two genes encoding protein phosphatase 2A catalytic subunits are differentially expressed in rice.

Plant Mol Biol 2003 Feb;51(3):295-311

Department of Biology and Chemistry, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong Special Administrative Region, People's Republic of China.

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http://dx.doi.org/10.1023/a:1022006023273DOI Listing
February 2003

G-box binding coincides with increased Solanum melongena cysteine proteinase expression in senescent fruits and circadian-regulated leaves.

Plant Mol Biol 2003 Jan;51(1):9-19

Department of Botany, University of Hong Kong, Pokfulam Road, Hong Kong, China.

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http://dx.doi.org/10.1023/a:1020859518877DOI Listing
January 2003

Tobacco-expressed Brassica juncea chitinase BjCHI1 shows antifungal activity in vitro.

Plant Mol Biol 2002 Sep;50(2):283-94

Department of Botany, University of Hong Kong, Hong Kong, China.

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http://dx.doi.org/10.1023/a:1016067200148DOI Listing
September 2002

[BjCHI1 from Brassica juncea displays both chitinase and agglutination activity].

Sheng Wu Gong Cheng Xue Bao 2002 Sep;18(5):572-7

Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences, Beijing 100081, China.

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September 2002