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Increased expression of miR-187 in human islets from individuals with type 2 diabetes is associated with reduced glucose-stimulated insulin secretion

Diabetologia, 2014-01, Vol.57 (1), p.122-128

2014

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An alternative polyadenylation signal in TCF7L2 generates isoforms that inhibit T cell factor/lymphoid-enhancer factor (TCF/LEF)-dependent target genes

Diabetologia, 2011-12, Vol.54 (12), p.3078-3082

2011

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Messenger RNA processing and its role in diabetes

Diabetic medicine, 2011-09, Vol.28 (9), p.1010-1017

Harries, L. W.

2011

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Partial and whole gene deletion mutations of the GCK and HNF1A genes in maturity-onset diabetes of the young

Diabetologia, 2007-11, Vol.50 (11), p.2313-2317

2007

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Identification of genetic polymorphisms at the glutathione S-transferase Pi locus and association with susceptibility to bladder, testicular and prostate cancer

Carcinogenesis (New York), 1997-04, Vol.18 (4), p.641-644

1997

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The position of premature termination codons in the hepatocyte nuclear factor -1 beta gene determines susceptibility to nonsense-mediated decay

Human genetics, 2005-11, Vol.118 (2), p.214-224

2005

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Severe Intrauterine Growth Retardation and Atypical Diabetes Associated with a Translocation Breakpoint Disrupting Regulation of the Insulin-Like Growth Factor 2 Gene

The journal of clinical endocrinology and metabolism, 2008-11, Vol.93 (11), p.4373-4380

2008

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The species origin of the cellular microenvironment influences markers of beta cell fate and function in EndoC-βH1 cells

Experimental cell research, 2017-12, Vol.361 (2), p.284-291

2017

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Negligible senescence in naked mole rats may be a consequence of well-maintained splicing regulation

GeroScience, 2020-04, Vol.42 (2), p.633-651

2020

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Genotypes of glutathione transferase M1 and P1 and their significance for lung DNA adduct levels and cancer risk

Carcinogenesis (New York), 1997-07, Vol.18 (7), p.1285-1289

1997

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Reduced peripheral blood mitochondrial DNA content is not a risk factor for Type 2 diabetes

Diabetic medicine, 2007-07, Vol.24 (7), p.784-787

2007

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Abnormal splicing of hepatocyte nuclear factor-1 beta in the renal cysts and diabetes syndrome

Diabetologia, 2004-05, Vol.47 (5), p.937-942

2004

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Novel monogenic diabetes mutations in the P2 promoter of the HNF4A gene are associated with impaired function in vitro

Diabetic medicine, 2010-06, Vol.27 (6), p.631-635

2010

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Variants in the isoform-specific coding regions of the HNF1A, HNF4A and HNF1B genes are not a common cause of familial, young-onset diabetes or renal cysts and diabetes (RCAD)

Diabetic medicine, 2009-05, Vol.26 (5), p.569-570

2009

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Molecular genetics of the human cytochrome P450 monooxygenase superfamily

Xenobiotica, 1998, Vol.28 (12), p.1129-1165

1998

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Genomics and successful aging: grounds for renewed optimism?

The journals of gerontology. Series A, Biological sciences and medical sciences, 2012-05, Vol.67 (5), p.511-519

2012

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Analysis of haematopoietic chimaerism by quantitative real-time polymerase chain reaction

Bone marrow transplantation (Basingstoke), 2005-02, Vol.35 (3), p.283-290

2005

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Gene transcripts associated with muscle strength: a CHARGE meta-analysis of 7,781 persons

Physiological genomics, 2016-01, Vol.48 (1), p.1-11

2016

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Abnormal splicing of hepatocyte nuclear factor 1 alpha in maturity-onset diabetes of the young

Diabetologia, 2002-10, Vol.45 (10), p.1463-1467

2002

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Expression profiling of type 2 diabetes susceptibility genes in the pancreatic islets, adipose tissue and liver of obese mice

Experimental and clinical endocrinology & diabetes, 2013-07, Vol.121 (7), p.413-419

2013

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Erratum to: An alternative polyadenylation signal in TCF7L2 generates isoforms that inhibit T cell factor/lymphoid-enhancer factor (TCF/LEF)-dependent target genes

Diabetologia, 2011, Vol.54 (12), p.3170-3170

2011

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Hepatocyte nuclear factor-1 gene deletions--a common cause of renal disease

Nephrology, dialysis, transplantation, 2007-10, Vol.23 (2), p.627-635

2007

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Permanent Neonatal Diabetes Caused by Dominant, Recessive, or Compound Heterozygous SUR1 Mutations with Opposite Functional Effects

American journal of human genetics, 2007-08, Vol.81 (2), p.375-382

2007

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Low prevalence of mitochondrial DNA 3243A>G point mutation in Caucasians with unexplained renal disease

Diabetic medicine, 2007-07, Vol.24 (7), p.804-806

2007

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Large variation in t(11;14)(q13;q32) and t(14;18)(q32;q21) translocation product size is confirmed by sequence analysis of PCR products

Clinical and laboratory haematology, 2006-08, Vol.28 (4), p.248-253

2006

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Increased expression of miR-187 in human islets from individuals with type 2 diabetes is associated with reduced glucose-stimulated insulin secretion

An alternative polyadenylation signal in TCF7L2 generates isoforms that inhibit T cell factor/lymphoid-enhancer factor (TCF/LEF)-dependent target genes

Messenger RNA processing and its role in diabetes

Partial and whole gene deletion mutations of the GCK and HNF1A genes in maturity-onset diabetes of the young

Identification of genetic polymorphisms at the glutathione S-transferase Pi locus and association with susceptibility to bladder, testicular and prostate cancer

The position of premature termination codons in the hepatocyte nuclear factor -1 beta gene determines susceptibility to nonsense-mediated decay

Severe Intrauterine Growth Retardation and Atypical Diabetes Associated with a Translocation Breakpoint Disrupting Regulation of the Insulin-Like Growth Factor 2 Gene

The species origin of the cellular microenvironment influences markers of beta cell fate and function in EndoC-βH1 cells

Negligible senescence in naked mole rats may be a consequence of well-maintained splicing regulation

Genotypes of glutathione transferase M1 and P1 and their significance for lung DNA adduct levels and cancer risk

Reduced peripheral blood mitochondrial DNA content is not a risk factor for Type 2 diabetes

Abnormal splicing of hepatocyte nuclear factor-1 beta in the renal cysts and diabetes syndrome

Novel monogenic diabetes mutations in the P2 promoter of the HNF4A gene are associated with impaired function in vitro

Variants in the isoform-specific coding regions of the HNF1A, HNF4A and HNF1B genes are not a common cause of familial, young-onset diabetes or renal cysts and diabetes (RCAD)

Molecular genetics of the human cytochrome P450 monooxygenase superfamily

Genomics and successful aging: grounds for renewed optimism?

Analysis of haematopoietic chimaerism by quantitative real-time polymerase chain reaction

Gene transcripts associated with muscle strength: a CHARGE meta-analysis of 7,781 persons

Abnormal splicing of hepatocyte nuclear factor 1 alpha in maturity-onset diabetes of the young

Expression profiling of type 2 diabetes susceptibility genes in the pancreatic islets, adipose tissue and liver of obese mice

Erratum to: An alternative polyadenylation signal in TCF7L2 generates isoforms that inhibit T cell factor/lymphoid-enhancer factor (TCF/LEF)-dependent target genes

Hepatocyte nuclear factor-1 gene deletions--a common cause of renal disease

Permanent Neonatal Diabetes Caused by Dominant, Recessive, or Compound Heterozygous SUR1 Mutations with Opposite Functional Effects

Low prevalence of mitochondrial DNA 3243A>G point mutation in Caucasians with unexplained renal disease

Large variation in t(11;14)(q13;q32) and t(14;18)(q32;q21) translocation product size is confirmed by sequence analysis of PCR products

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