Gene and Phenotype Analysis of Congenital Generalized Lipodystrophy in Japanese: A Novel Homozygous Nonsense Mutation in Seipin Gene-Reference-Cited by-同舟云学术

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Gene and Phenotype Analysis of Congenital Generalized Lipodystrophy in Japanese: A Novel Homozygous Nonsense Mutation in Seipin Gene

Published:2004-05 Issue:5 Volume:89 Page:2360-2364
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Ebihara Ken,Kusakabe Toru,Masuzaki Hiroaki,Kobayashi Nozomi,Tanaka Tomohiro,Chusho Hideki,Miyanaga Fumiko,Miyazawa Takashi,Hayashi Tatsuya,Hosoda Kiminori,Ogawa Yoshihiro,Nakao Kazuwa

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 41 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Seipin is involved in oxygen-glucose deprivation/reoxygenation induced neuroinflammation by regulating the TLR3/TRAF3/NF-κB pathway;International Immunopharmacology;2024-06

2. Role of Seipin in Human Diseases and Experimental Animal Models;Biomolecules;2022-06-17

3. RNA-seq of peripheral blood mononuclear cells of congenital generalized lipodystrophy type 2 patients;Scientific Data;2021-10-13

4. La vie sans tissu adipeux : les lipodystrophies généralisées congénitales ; causes, physiopathologie et prise en charge thérapeutique;Médecine des Maladies Métaboliques;2021-03

5. Practice guideline for lipodystrophy syndromes—clinically important diseases of the Japan Endocrine Society (JES);Endocrine Journal;2021

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