Genetic deletion of a short fragment of glucokinase in rabbit by CRISPR/Cas9 leading to hyperglycemia and other typical features seen in MODY-2-Reference-Cited by-同舟云学术

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Genetic deletion of a short fragment of glucokinase in rabbit by CRISPR/Cas9 leading to hyperglycemia and other typical features seen in MODY-2

Published:2019-11-13 Issue:16 Volume:77 Page:3265-3277
ISSN:1420-682X
Container-title:Cellular and Molecular Life Sciences
language:en
Short-container-title:Cell. Mol. Life Sci.

Author:

Song Yuning,Sui Tingting,Zhang Yuxin,Wang Yong,Chen Mao,Deng Jichao,Chai Zhonglin,Lai Liangxue,Li Zhanjun^ORCID

Funder

the National Key Research and Development Program of China Stem Cell and Translational Research

The Strategic Priority Research Program of the Chinese Academy of Sciences

Guangdong Province science and technology plan project

China Postdoctoral Science Foundation Funded Project

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Cellular and Molecular Neuroscience,Pharmacology,Molecular Biology,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00018-019-03354-4.pdf

Reference45 articles.

1. Ellard S, Bellanne-Chantelot C, Hattersley AT, European Molecular Genetics Quality Network MG (2008) Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young. Diabetologia 51:546–553

2. Matschinsky F, Liang Y, Kesavan P, Wang L, Froguel P, Velho G, Cohen D, Permutt MA, Tanizawa Y, Jetton TL et al (1993) Glucokinase as pancreatic beta cell glucose sensor and diabetes gene. J Clin Investig 92:2092–2098

3. Dimitriadis G, Boutati E, Raptis SA (2007) The importance of adipose tissue in diabetes pathophysiology and treatment. Hormone Metab Res 39:705–706

4. Stenson PD, Mort M, Ball EV, Howells K, Phillips AD, Thomas NS, Cooper DN (2009) The human gene mutation database: 2008 update. Genome Med 1:13

5. Osbak KK, Colclough K, Saint-Martin C, Beer NL, Bellanne-Chantelot C, Ellard S, Gloyn AL (2009) Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia. Hum Mutat 30:1512–1526

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