John E A Common

John E A Common

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John E A Common

John E A Common

Publications by authors named "John E A Common"

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Biotherapeutic Approaches in Atopic Dermatitis.

Biotechnol J 2020 Mar 16:e1900322. Epub 2020 Mar 16.

Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

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http://dx.doi.org/10.1002/biot.201900322DOI Listing
March 2020

Belinostat resolves skin barrier defects in atopic dermatitis by targeting the dysregulated miR-335:SOX6 axis.

J Allergy Clin Immunol 2020 Feb 21. Epub 2020 Feb 21.

Skin Research Institute of Singapore, Agency for Science Technology & Research, Singapore; Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Program in Cancer and Stem Cell Biology, Duke-NUS Medical School, Singapore. Electronic address:

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http://dx.doi.org/10.1016/j.jaci.2020.02.007DOI Listing
February 2020

Induced pluripotent stem cell line heterozygous for p.R501X mutation in filaggrin: KCLi003-A.

Stem Cell Res 2019 08 7;39:101527. Epub 2019 Aug 7.

Stem Cell Laboratory, Department of Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK; Assisted Conception Unit, Guy's Hospital, London, UK. Electronic address:

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http://dx.doi.org/10.1016/j.scr.2019.101527DOI Listing
August 2019

Reduced Microbial Diversity Is a Feature of Recessive Dystrophic Epidermolysis Bullosa-Involved Skin and Wounds.

J Invest Dermatol 2018 11 16;138(11):2492-2495. Epub 2018 May 16.

Department of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA. Electronic address:

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http://dx.doi.org/10.1016/j.jid.2018.04.026DOI Listing
November 2018

Assays to Study Consequences of Cytoplasmic Intermediate Filament Mutations: The Case of Epidermal Keratins.

Methods Enzymol 2016 6;568:219-53. Epub 2016 Jan 6.

Institute of Medical Biology, Singapore. Electronic address:

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http://dx.doi.org/10.1016/bs.mie.2015.09.030DOI Listing
October 2016

Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria.

PLoS One 2014 3;9(2):e87250. Epub 2014 Feb 3.

Shandong Provincial Institute of Dermatology and Venereology, Provincial Academy of Medical Science, Jinan, Shandong, China ; Shandong Provincial Hospital for Skin Diseases, Shandong University, Jinan, Shandong, China ; Shandong Provincial Key Lab for Dermatovenereology, Jinan, Shandong, China ; Shandong Provincial Medical Center for Dermatovenereology, Jinan, Shandong, China ; Shandong Clinical College, Anhui Medical University, Jinan, Shandong, China.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0087250PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3911924PMC
December 2014

Fabrication of a 3D hair follicle-like hydrogel by soft lithography.

J Biomed Mater Res A 2013 Nov 30;101(11):3159-69. Epub 2013 Mar 30.

Department of Pharmacy, National University of Singapore, 18 Science Drive 4, Singapore, 117543, Singapore.

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http://staff.science.nus.edu.sg/~phakl/130414%20hair%20onlin
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http://doi.wiley.com/10.1002/jbm.a.34628
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http://dx.doi.org/10.1002/jbm.a.34628DOI Listing
November 2013

'See-saw' expression of microRNA-198 and FSTL1 from a single transcript in wound healing.

Nature 2013 Mar 10;495(7439):103-6. Epub 2013 Feb 10.

Institute of Medical Biology, Agency for Science Technology & Research (A*STAR), 138648, Singapore.

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http://dx.doi.org/10.1038/nature11890DOI Listing
March 2013

Developmental expression of the fermitin/kindlin gene family in Xenopus laevis embryos.

Dev Dyn 2011 Aug;240(8):1958-63

Institute of Medical Biology, A*STAR, Singapore.

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http://dx.doi.org/10.1002/dvdy.22683DOI Listing
August 2011

Clinical and genetic heterogeneity of erythrokeratoderma variabilis.

J Invest Dermatol 2005 Nov;125(5):920-7

Centre for Cutaneous Research, Institute of Cell and Molecular Science, Barts and the London School of Medicine and Dentistry, Queen Mary, University of London, Whitechapel, London, UK.

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http://dx.doi.org/10.1111/j.0022-202X.2005.23919.xDOI Listing
November 2005

Connexin interaction patterns in keratinocytes revealed morphologically and by FRET analysis.

J Cell Sci 2005 Apr 15;118(Pt 7):1505-14. Epub 2005 Mar 15.

Centre for Cutaneous Research, Institute of Cell and Molecular Science, Barts and the London School of Medicine and Dentistry, Queen Mary, University of London, 4 Newark Street, London E1 2AT, UK.

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http://dx.doi.org/10.1242/jcs.01733DOI Listing
April 2005

Cellular mechanisms of mutant connexins in skin disease and hearing loss.

Cell Commun Adhes 2003 Jul-Dec;10(4-6):347-51

Centre for Cutaneous Research, Barts and the London School of Medicine and Dentistry, Queen Mary, University of London, Whitechapel, London, United Kingdom.

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http://dx.doi.org/10.1080/cac.10.4-6.347.351DOI Listing
November 2004

Functional studies of human skin disease- and deafness-associated connexin 30 mutations.

Biochem Biophys Res Commun 2002 Nov;298(5):651-6

Centre for Cutaneous Research, Barts and the London School of Medicine and Dentistry, Queen Mary, University of London, Whitechapel, UK.

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http://dx.doi.org/10.1016/s0006-291x(02)02517-2DOI Listing
November 2002

Defective trafficking and cell death is characteristic of skin disease-associated connexin 31 mutations.

Hum Mol Genet 2002 Aug;11(17):2005-14

Centre for Cutaneous Research, Barts and the London School of Medicine and Dentistry, Queen Mary, University of London, Whitechapel, London E1 2AT, UK.

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http://dx.doi.org/10.1093/hmg/11.17.2005DOI Listing
August 2002