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Lynn E. Pritchard

Wellcome Trust Centre for Human Genetics

15

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Processing of proglucagon to GLP-1 in pancreatic α-cells: is this a paracrine mechanism enabling GLP-1 to act on β-cells?

2011 Journal of Endocrinology
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Reduced appetite and body mass index with delayed puberty in a mother and son: association with a rare novel sequence variant in the leptin gene.

2011 European Journal of Endocrinology
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Manipulation of proprotein convertase 1 expression in AtT20 cells changes proopiomelanocortin processing and trafficking: Implications for ACTH regulatory pathways

2007
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A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism

2002 Human Molecular Genetics
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Genetic analysis of chromosome 2 in Type 1 diabetes. Analysis of putative loci IDDM7, IDDM12, and IDDM13 and candidate genes NRAMP1 and IA-2 and the interleukin-1 gene cluster

1998 Diabetes
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A search for type 1 diabetes susceptibility genes in families from the United Kingdom

1998 Nature Genetics
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The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry.

1996 Human Molecular Genetics
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Mutation of the glucagon receptor gene and diabetes mellitus in the UK: association or founder effect?

1995 Human Molecular Genetics
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Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus

1995 Nature Genetics
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Analysis of the CD3 gene region and type 1 diabetes: application of fluorescence-based technology to linkage disequilibrium mapping

1995 Human Molecular Genetics
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