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Scholar Results 1 - 10 of about 101 related to Stride: β-cell dysfunction, insulin sensitivity, and glycosuria precede diabetes in hepatocyte.... (0.09 sec) 

β-cell dysfunction, insulin sensitivity, and glycosuria precede diabetes in …

- diabetesjournals.org
A Stride, S Ellard, P Clark, L Shakespeare, M … - Diabetes care, 2005 - Am Diabetes Assoc
RESULTS—HNF-1α mutations were found in 20 offspring, 7 with diabetes and 13 without
diabetes. The 13 nondiabetic mutation carriers were compared with 27 family control
subjects, who were matched for age, sex, and BMI. There was marked β-cell deficiency ...
Cited by 21 - Related articles - BL Direct - All 5 versions

Isomers of the TCF1 gene encoding hepatocyte nuclear factor-1 alpha show …

- oxfordjournals.org
LW Harries, S Ellard, A Stride… - Human Molecular Genetics, 2006 - Oxford Univ Press
The generation of multiple transcripts by mRNA processing has the potential to moderate differences
in gene expression both between tissues and at different stages of development. Where gene
function is compromised by mutation, the presence of multiple isoforms may influence the ...
Cited by 21 - Related articles - BL Direct - All 6 versions

Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte …


ER Pearson, S Pruhova, CJ Tack, A Johansen, HAJ … - Diabetologia, 2005 - Springer
Page 1. Diabetologia (2005) 48: 878–885 DOI 10.1007/s00125-005-1738-y ARTICLE ER
Pearson . S. Pruhova . CJ Tack . A. Johansen . HAJ Castleden . PJ Lumb . AS Wierzbicki .
PM Clark . J. Lebl . O. Pedersen . S. Ellard . T. Hansen . AT Hattersley ...
Cited by 57 - Related articles - All 5 versions

[PDF] Genetic testing for glucokinase mutations in clinically selected patients with MODY: …


S Schnyder, PE Mullis, S Ellard, AT Hattersley, CE … - Swiss Medical Weekly, 2005 - smw.ch
The differential diagnosis for children with diabetes includes a group of monogenic diabetic disorders
known as maturity-onset diabetes of the young (MODY). So far, six underlying gene de- fects
have been identified. The most common sub- types are caused by mutations in the genes ...
Cited by 11 - Related articles - View as HTML - BL Direct - All 3 versions

Hepatocyte nuclear factor-1 beta mutations cause neonatal diabetes and …


EL Edghill, C Bingham, AS Slingerland, JA … - Diabetic …, 2006 - interscience.wiley.com
Aim The transcription factor hepatocyte nuclear factor-1beta (HNF-1β) is expressed in rodent
pancreatic progenitor cells, where it is an important member of the genetic hierarchy that regulates
the generation of pancreatic endocrine and exocrine cells. The recent description of an ...
Cited by 25 - Related articles - BL Direct - All 4 versions

Neonatal Diabetes Mellitus and Neonatal Polycystic, Dysplastic Kidneys: …

- endojournals.org
T Yorifuji, K Kurokawa, M Mamada, T Imai, M … - Journal of Clinical …, 2004 - Endocrine Soc
Mutations in the gene coding for hepatocyte nuclear factor-1ß (HNF-1ß) have been known to
cause a form of maturity-onset diabetes of the young (MODY5), which is usually characterized
by dominantly inherited adolescence-onset diabetes mellitus associated with renal cysts. ...
Cited by 30 - Related articles - BL Direct - All 4 versions

Mutations in the genes encoding the transcription factors hepatocyte nuclear factor …


S Ellard, K Colclough - Human mutation, 2006 - interscience.wiley.com
Maturity-onset diabetes of the young (MODY) is a monogenic form of diabetes mellitus characterized
by autosomal dominant inheritance, early age of onset (often <25 years of age), and pancreatic
-cell dysfunction. MODY is both clinically and genetically heterogeneous, with six different ...
Cited by 33 - Related articles - BL Direct - All 4 versions

MODY in Iceland is associated with mutations in HNF-1α and a novel mutation in …


SY Kristinsson, ET Thorolfsdottir, B Talseth, E … - Diabetologia, 2001 - Springer
Maturity-onset diabetes of the young (MODY) is a subgroup of diabetes which is inherited and
which could account for 2±5% of Type II diabetic patients [1]. Information on rare monogenic
forms of diabetes could shed light on the development of the more common multigenic ...
Cited by 49 - Related articles - BL Direct - All 9 versions

The genetic abnormality in the beta cell determines the response to an oral …


A Stride, M Vaxillaire, T Tuomi, F Barbetti, PR Njølstad, … - Diabetologia, 2002 - Springer
Diabetes is defined on the basis of both fasting glu- cose concentration and the glucose concentration
2 h following a glucose load. Recent revisions by the American Diabetes Association (ADA) and
World Health Organisation (WHO) have put more empha- sis on the fasting value as it is ...
Cited by 75 - Related articles - BL Direct - All 4 versions

Aetiological heterogeneity of asymptomatic hyperglycaemia in children and …


E Feigerlova, Š Pruhová, L Dittertova, J Lebl, D … - European journal of …, 2006 - Springer
Page 1. Eur J Pediatr (2006) 165: 446–452 DOI 10.1007/s00431-006-0106-3 ORIGINAL PAPER
E. Feigerlová . Š. Pruhová . L. Dittertová . J. Lebl . D. Pinterová . K. Kološtová . M. Černá . O.
Pedersen . T. Hansen Aetiological heterogeneity of asymptomatic hyperglycaemia ...
Cited by 13 - Related articles - BL Direct - All 3 versions


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