Jacqueline K White

Jacqueline K White

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Jacqueline K White

Publications by authors named "Jacqueline K White"

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Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.

Commun Biol 2019 7;2:97. Epub 2019 Mar 7.

Department of Ophthalmology & Vision Science, School of Medicine, U.C. Davis, Sacramento, CA, 95817, USA.

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http://dx.doi.org/10.1038/s42003-019-0349-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6405960PMC
March 2019

Identification of genetic elements in metabolism by high-throughput mouse phenotyping.

Nat Commun 2018 01 18;9(1):288. Epub 2018 Jan 18.

German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Ingolstädter Landstr. 1, 85764, Neuherberg, Germany.

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http://dx.doi.org/10.1038/s41467-017-01995-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5773596PMC
January 2018

Corrigendum: High-throughput discovery of novel developmental phenotypes.

Nature 2017 11 8;551(7680):398. Epub 2017 Nov 8.

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http://dx.doi.org/10.1038/nature24643DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849394PMC
November 2017

Improving the Identification of Phenotypic Abnormalities and Sexual Dimorphism in Mice When Studying Rare Event Categorical Characteristics.

Genetics 2017 02 7;205(2):491-501. Epub 2016 Dec 7.

Department of Statistics and Operations Research, School of Mathematical Sciences, Tel Aviv University, Israel.

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http://dx.doi.org/10.1534/genetics.116.195388DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289831PMC
February 2017

Reporting phenotypes in mouse models when considering body size as a potential confounder.

J Biomed Semantics 2016 9;7. Epub 2016 Feb 9.

Mouse Informatics Group, Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire UK.

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http://dx.doi.org/10.1186/s13326-016-0050-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748495PMC
October 2016

High-throughput discovery of novel developmental phenotypes.

Nature 2016 09 14;537(7621):508-514. Epub 2016 Sep 14.

The Jackson Laboratory, Bar Harbor, Maine 04609, USA.

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http://dx.doi.org/10.1038/nature19356DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295821PMC
September 2016

MacroH2A1 isoforms are associated with epigenetic markers for activation of lipogenic genes in fat-induced steatosis.

FASEB J 2015 May 19;29(5):1676-87. Epub 2014 Dec 19.

*Foundation for Liver Research, Institute of Hepatology, London, United Kingdom; University College London (UCL)--Institute for Liver & Digestive Health, UCL Medical School, London, United Kingdom, Mouse Genetics Project, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, United Kingdom; and Physiology and Experimental Medicine Research Program, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada

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http://dx.doi.org/10.1096/fj.14-262717DOI Listing
May 2015

Mouse slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunction.

Invest Ophthalmol Vis Sci 2015 May;56(5):3015-26

MRC Human Genetics Unit, MRC Institute of Genetics & Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom 4Roslin Institute, University of Edinburgh, Edinburgh, United Kingdom.

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http://dx.doi.org/10.1167/iovs.14-15735DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4538965PMC
May 2015

Disruption of the potassium channel regulatory subunit KCNE2 causes iron-deficient anemia.

Exp Hematol 2014 Dec 12;42(12):1053-8.e1. Epub 2014 Aug 12.

Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, United Kingdom. Electronic address:

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http://dx.doi.org/10.1016/j.exphem.2014.07.269DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4271779PMC
December 2014

Identification of genes important for cutaneous function revealed by a large scale reverse genetic screen in the mouse.

PLoS Genet 2014 Oct 23;10(10):e1004705. Epub 2014 Oct 23.

Department of Biochemistry and Molecular Biology, Monash University, Clayton, Melbourne, Australia; Department of Anatomy and Developmental Biology, Monash University, Clayton, Melbourne, Australia.

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http://dx.doi.org/10.1371/journal.pgen.1004705DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207618PMC
October 2014

Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss.

PLoS Genet 2014 Oct 30;10(10):e1004688. Epub 2014 Oct 30.

Wellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom; Wolfson Centre for Age-Related Diseases, King's College London, London, United Kingdom.

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http://dx.doi.org/10.1371/journal.pgen.1004688DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214598PMC
October 2014

Large-scale mouse knockouts and phenotypes.

Wiley Interdiscip Rev Syst Biol Med 2012 Nov-Dec;4(6):547-63. Epub 2012 Aug 15.

Mouse Pipelines, Wellcome Trust Sanger Institute, Hinxton, UK.

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http://dx.doi.org/10.1002/wsbm.1183DOI Listing
February 2013

Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1.

Mamm Genome 2013 Feb 17;24(1-2):44-53. Epub 2012 Nov 17.

Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, UK.

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http://link.springer.com/10.1007/s00335-012-9438-7
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http://dx.doi.org/10.1007/s00335-012-9438-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560959PMC
February 2013

Generation of the Sotos syndrome deletion in mice.

Mamm Genome 2012 Dec 29;23(11-12):749-57. Epub 2012 Aug 29.

Experimental Cancer Genetics, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1HH, UK.

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http://dx.doi.org/10.1007/s00335-012-9416-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510424PMC
December 2012

The fallacy of ratio correction to address confounding factors.

Lab Anim 2012 Jul;46(3):245-52

Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK.

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http://dx.doi.org/10.1258/la.2012.012003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4152922PMC
July 2012

The mouse genetics toolkit: revealing function and mechanism.

Genome Biol 2011 Jun 24;12(6):224. Epub 2011 Jun 24.

Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK.

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http://dx.doi.org/10.1186/gb-2011-12-6-224DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218837PMC
June 2011

Optimising experimental design for high-throughput phenotyping in mice: a case study.

Mamm Genome 2010 Oct 27;21(9-10):467-76. Epub 2010 Aug 27.

Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.

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http://dx.doi.org/10.1007/s00335-010-9279-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974211PMC
October 2010

Influence of Slc11a1 (formerly Nramp1) on DSS-induced colitis in mice.

J Leukoc Biol 2009 Apr 30;85(4):703-10. Epub 2008 Dec 30.

Centre for Child Health Research, University of Western Australia, P.O. Box 855, West Perth, Western Australia, 6872, Australia.

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http://dx.doi.org/10.1189/jlb.0708397DOI Listing
April 2009

Slc11a1, formerly Nramp1, is expressed in dendritic cells and influences major histocompatibility complex class II expression and antigen-presenting cell function.

Infect Immun 2007 Oct 9;75(10):5059-67. Epub 2007 Jul 9.

Cambridge Institute for Medical Research and Department of Medicine, Wellcome Trust/MRC Building, University of Cambridge School of Clinical Medicine, Addenbrookes Hospital, Hills Road, Cambridge CB2 2XY, United Kingdom.

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http://dx.doi.org/10.1128/IAI.00153-07DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2044529PMC
October 2007

Slc11a1-mediated resistance to Salmonella enterica serovar Typhimurium and Leishmania donovani infections does not require functional inducible nitric oxide synthase or phagocyte oxidase activity.

J Leukoc Biol 2005 Mar 15;77(3):311-20. Epub 2004 Dec 15.

Wellcome Trust/MRC Building, University of Cambridge School of Clinical Medicine, Addenbrookes Hospital, Hills Road, Cambridge CB2 2XY, UK.

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http://dx.doi.org/10.1189/jlb.0904546DOI Listing
March 2005

Candidate gene association study of solute carrier family 11a members 1 (SLC11A1) and 2 (SLC11A2) genes in Alzheimer's disease.

Neurosci Lett 2005 Feb;374(2):124-8

Cambridge Institute for Medical Research, University of Cambridge School of Clinical Medicine, Wellcome Trust/MRC Building, Addenbrooke's Hospital, Hills Rd., Cambridge CB2 2XY, UK.

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http://dx.doi.org/10.1016/j.neulet.2004.10.038DOI Listing
February 2005

Incomplete glycosylation and defective intracellular targeting of mutant solute carrier family 11 member 1 (Slc11a1).

Biochem J 2004 Sep;382(Pt 3):811-9

Cambridge Institute for Medical Research, University of Cambridge School of Clinical Medicine, Wellcome Trust/MRC Building, Addenbrooke's Hospital, Hills Road, Cambridge CB2 2XY, UK.

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http://biochemj.org/lookup/doi/10.1042/BJ20040808
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http://dx.doi.org/10.1042/BJ20040808DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1133956PMC
September 2004

Comparative analysis of two slc11 (Nramp) loci in Takifugu rubripes.

DNA Cell Biol 2004 Jan;23(1):45-58

Division of Environmental and Evolutionary Biology, The Gatty Marine Laboratory, University of St. Andrews, Fife KY16 8LB, UK.

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http://dx.doi.org/10.1089/104454904322745925DOI Listing
January 2004

Divalent cation transport and susceptibility to infectious and autoimmune disease: continuation of the Ity/Lsh/Bcg/Nramp1/Slc11a1 gene story.

Immunol Lett 2003 Jan;85(2):197-203

Cambridge Institute for Medical Research, School of Clinical Medicine, University of Cambridge, Wellcome Trust/MRC Building, Addenbrooke's Hospital, Hills Road, Cambridge CB2 2XY, UK.

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http://dx.doi.org/10.1016/s0165-2478(02)00231-6DOI Listing
January 2003