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Scholar Results 1 - 10 of about 101 related to del Bosque-Plata: Mutations in the coding region of the neurogenin 3 gene (NEUROG3) are not.... (0.11 sec) 

Mutations in the coding region of the neurogenin 3 gene (NEUROG3) are not a …


L del Bosque-Plata, J Lin, Y Horikawa, PEH Schwarz, … - Diabetes, 2001 - Am Diabetes Assoc
Mutations in transcription factors that play a role in the development of the endocrine
pancreas, such as insulin promoter factor-1 and NeuroD1/BETA2, have been associated with
diabetes. Cell type–specific members of the basic helix-loop-helix (bHLH) family of ...
Cited by 8 - Related articles - BL Direct - All 6 versions

Polymorphisms in the neurogenin 3 gene (NEUROG) and their relation to altered …


JN Jensen, L Hansen, CT Ekstrøm, F Pociot, J Nerup, T … - Diabetologia, 2001 - Springer
HNF-1b, the insulin promotor factor (IPF)-1 and neuronal determation factor (NeuroD). The
NEU- ROG3 is a new member of the subfamily of basic-he- lix-loop-helix (bHLH) class B transcription
factors involved in triggering NeuroD expression in the en- docrine pancreatic precursor ...
Cited by 7 - Related articles - BL Direct - All 3 versions

beta-cell transcription factors and diabetes: no evidence for diabetes-associated …

- diabetesjournals.org [PDF] 
Y Horikawa, NJ Cox, N Iwasaki, M Ogata, Y Iwamoto, V … - Diabetes, 2000 - Am Diabetes Assoc
The basic helix-loop-helix (bHLH) family of transcrip- tion factors plays an important role in the
normal development and function of the endocrine pancreas. Heterozygous mutations in the
gene encoding one member of this family, NeuroD1/BETA2, are associated with a ...
Cited by 5 - Related articles - BL Direct - All 4 versions

Variants of neurogenin 3 gene are not associated with Type II diabetes in …


T Okada, K Tobe, K Hara, K Yasuda, Y Kawaguchi, H … - Diabetologia, 2001 - Springer
Variants of IPF-1 [2, 3] and NeuroD [4] have also been reported to be related to the development
of Type II diabetes. Neurogenins are a set of basic helix-loop-helix (bHLH) transcription factors
which are essential for the determination of neuronal tissues during embry- onic ...
Cited by 2 - Related articles - BL Direct - All 4 versions

Insulin gene mutations as cause of diabetes in children negative for five type 1 …


R Bonfanti, C Colombo, V Nocerino, O Massa, V … - Diabetes Care, 2009 - Am Diabetes Assoc
OBJECTIVE—Heterozygous, gain-of-function mutations of the insulin gene can cause permanent
diabetes with onset ranging from the neonatal period through adulthood. The aim of our study
was to screen for the insulin gene in patients who had been clinically classified as type 1 ...
Cited by 4 - Related articles - All 3 versions

Mutation screening of the neurogenin-3 gene in autosomal dominant diabetes

- endojournals.org
SH Kim, JH Warram, AS Krolewski, A Doria - Journal of Clinical …, 2001 - Endocrine Soc
We investigated whether genetic variability in neurogenin-3, a basic helix-loop-helix transcription
factor that is expressed in the developing pancreas, contributes to the etiology of maturity-onset
diabetes of the young or other forms of autosomal dominant diabetes. Ninety-one ...
Cited by 5 - Related articles - BL Direct - All 4 versions

Identification of three missense mutations in the peroxisome proliferator-activated …


M Hara, X Wang, VP Paz, N Iwasaki, M Honda, Y … - Journal of Human …, 2001 - Springer
M. Hara ( ) · X. Wang · VP Paz · GI Bell Howard Hughes Medical Institute, The University of
Chicago, 5841 South Maryland Avenue, MC1028, Chicago, IL 60637, USA Tel. 1-773-702-9118
; Fax 1-773-702-9237 e-mail: mhara@midway.uchicago.edu N. Iwasaki · Y. Iwamoto ...
Cited by 8 - Related articles - BL Direct - All 5 versions

[CITATION] Mutations in IAPP and NEUROG3 genes are not a common cause of permanent …


F Barbetti, V Nocerino, C Colombo, R Bonfanti, D … - interscience.wiley.com
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[CITATION] Mutations in IAPP and NEUROG3 genes are not a common cause of permanent …


V Nocerino, C Colombo, R Bonfanti, D Iafusco … - Diabetic medicine: a …, 2009 - ncbi.nlm.nih.gov
1: Diabet Med. 2009 Jun;26(6):660-1. Mutations in IAPP and NEUROG3 genes are
not a common cause of permanent neonatal/infancy/childhood-onset diabetes. Nocerino
V, Colombo C, Bonfanti R, Iafusco D, Barbetti F. Publication ...
Related articles - All 2 versions

Transcription factor expression in the developing human fetal endocrine pancreas


BM Lyttle, J Li, M Krishnamurthy, F Fellows, MB … - Diabetologia, 2008 - Springer
Abstract Aims/hypothesis Morphological changes that occur during pancreatic endocrine cell
differentiation have been shown in rodent systems to be dependent on sequential alterations
in transcription factor expression. However, similar data for humans have been limited. ...
Cited by 11 - Related articles - BL Direct - All 2 versions


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