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Localization of MODY3 to a 5-cM region of human chromosome 12. [electronic resource] by
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Mice conditionally lacking the Wolfram gene in pancreatic islet beta cells exhibit diabetes as a result of enhanced endoplasmic reticulum stress and apoptosis. [electronic resource] by
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AATF mediates an antiapoptotic effect of the unfolded protein response through transcriptional regulation of AKT1. [electronic resource] by
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Wolfram syndrome 1 gene negatively regulates ER stress signaling in rodent and human cells. [electronic resource] by
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- Ishihara, Hisamitsu
- Oka, Yoshitomo
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Linkage analysis of glucokinase gene with NIDDM in Caucasian pedigrees. [electronic resource] by
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A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism. [electronic resource] by
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- Wilson, B A
- Glaser, B
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Clinical characteristics of subjects with a missense mutation in glucokinase. [electronic resource] by
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- Wainscoat, J S
- Permutt, M A
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Familial hyperinsulinism caused by an activating glucokinase mutation. [electronic resource] by
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- Stanley, C A
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Glucokinase gene in gestational diabetes mellitus: population association study and molecular scanning. [electronic resource] by
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- Acton, R T
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In:
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Impact of polymorphisms in WFS1 on prediabetic phenotypes in a population-based sample of middle-aged people with normal and abnormal glucose regulation. [electronic resource] by
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- Permutt, M A
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Common variants of the hepatocyte nuclear factor-4alpha P2 promoter are associated with type 2 diabetes in the U.K. population. [electronic resource] by
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- Shields, Beverley
- Hitman, Graham
- Walker, Mark
- McCarthy, Mark I
- Love-Gregory, Latisha D
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Identification and functional analysis of sulfonylurea receptor 1 variants in Japanese patients with NIDDM. [electronic resource] by
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- Hosaka, T
- Ueda, K
- Matsutani, A
- Repunte, V P
- Yamada, M
- Kurachi, Y
- Bryan, J
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Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations. [electronic resource] by
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- Polonsky, K
- Glaser, B
- Permutt, M A
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- Stafford, D
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- Baker, L
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Variants in the CD36 gene associate with the metabolic syndrome and high-density lipoprotein cholesterol. [electronic resource] by
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- Sun, Lingwei
- Wasson, Jon
- Schappe, Timothy
- Doria, Alessandro
- Rao, D C
- Hunt, Steven C
- Klein, Samuel
- Neuman, Rosalind J
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In:
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Sequence variants in the pancreatic islet beta-cell inwardly rectifying K+ channel Kir6.2 (Bir) gene: identification and lack of role in Caucasian patients with NIDDM. [electronic resource] by
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- Ferrer, J
- Warren-Perry, M
- Zhang, Y
- Millns, H
- Turner, R C
- Elbein, S C
- Hampe, C L
- Suarez, B K
- Inagaki, N
- Seino, S
- Permutt, M A
Producer: 19970314
In:
Diabetes vol. 46
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