A novel mutation, Ser159Pro in the NeuroD1/BETA2 gene contributes to the development of diabetes in a Chinese potential MODY family (Q80172922)

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29 December 2019

title

A novel mutation, Ser159Pro in the NeuroD1/BETA2 gene contributes to the development of diabetes in a Chinese potential MODY family (English)

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29 December 2019

author name string

Limei Liu

1

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29 December 2019

Hiroto Furuta

2

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29 December 2019

Asako Minami

3

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29 December 2019

Taishan Zheng

4

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29 December 2019

Weiping Jia

5

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29 December 2019

Kishio Nanjo

6

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29 December 2019

Kunsan Xiang

7

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29 December 2019

publication date

18 April 2007

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Molecular and Cellular Biochemistry

29 December 2019

published in

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29 December 2019

volume

303

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29 December 2019

issue

1-2

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29 December 2019

page(s)

115-120

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https://scigraph.springernature.com/pub.10.1007/s11010-007-9463-0

29 December 2019

exact match

0 references

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Ala45Thr variation in neuroD1 gene is associated with early-onset type 2 diabetes with or without diabetic pedigree in Chinese.

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Systematic search for single nucleotide polymorphisms in the insulin gene: evidence for a high frequency of -23T-->A in Japanese subjects

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The NeuroD1/BETA2 sequences essential for insulin gene transcription colocalize with those necessary for neurogenesis and p300/CREB binding protein binding

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Familial early-onset type 2 diabetes in Chinese patients: obesity and genetics have more significant roles than autoimmunity

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Insulin promoter factor 1 gene is not a major cause of maturity-onset diabetes of the young in French Caucasians

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Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus

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Beta-cell transcription factors and diabetes: mutations in the coding region of the BETA2/NeuroD1 (NEUROD1) and Nkx2.2 (NKX2B) genes are not associated with maturity-onset diabetes of the young in Japanese

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beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors

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Mutations in hepatocyte nuclear factor 1beta are not a common cause of maturity-onset diabetes of the young in the U.K.

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Molecular genetics of diabetes mellitus in Chinese subjects: identification of mutations in glucokinase and hepatocyte nuclear factor-1alpha genes in patients with early-onset type 2 diabetes mellitus/MODY.

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12 December 2020

Tissue-specific regulation of the insulin gene by a novel basic helix-loop-helix transcription factor

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