Mouse Samd9l is not a functional paralogue of the human SAMD9, the gene mutated in normophosphataemic familial tumoral calcinosis-Reference-Cited by-同舟云学术

Mouse Samd9l is not a functional paralogue of the human SAMD9, the gene mutated in normophosphataemic familial tumoral calcinosis

Published:2012-06-20 Issue:7 Volume:21 Page:554-556
ISSN:0906-6705
Container-title:Experimental Dermatology
language:en
Short-container-title:Exp Dermatol

Author:

Li Qiaoli¹,Guo Haitao¹,Matsui Hirotaka²,Honda Hiroaki³,Inaba Toshiya²,Sundberg John P.⁴,Sprecher Eli⁵,Uitto Jouni¹

Affiliation:

1. Department of Dermatology and Cutaneous Biology; Jefferson Medical College; Jefferson Institute of Molecular Medicine; Thomas Jefferson University; Philadelphia; PA; USA

2. Department of Molecular Oncology; Research Institute for Radiation Biology & Medicine; Hiroshima University; Hiroshima; Japan

3. Department of Disease Model; Research Institute for Radiation Biology & Medicine; Hiroshima University; Hiroshima; Japan

4. The Jackson Laboratory; Bar Harbor; ME; USA

5. Department of Dermatology; Tel Aviv Sourasky Medical Center; Tel Aviv; Israel

Publisher

Wiley

Subject

Dermatology,Molecular Biology,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0625.2012.01524.x/fullpdf

Reference13 articles.

1. Familial Tumoral Calcinosis: From Characterization of a Rare Phenotype to the Pathogenesis of Ectopic Calcification

2. A Deleterious Mutation in SAMD9 Causes Normophosphatemic Familial Tumoral Calcinosis

3. Normophosphatemic Familial Tumoral Calcinosis Is Caused by Deleterious Mutations in SAMD9, Encoding a TNF-α Responsive Protein

4. Human sterile alpha motif domain 9, a novel gene identified as down-regulated in aggressive fibromatosis, is absent in the mouse

5. The Samd9L Gene: Transcriptional Regulation and Tissue-Specific Expression in Mouse Development

Cited by 3 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. A paralogous pair of mammalian host restriction factors form a critical host barrier against poxvirus infection;PLOS Pathogens;2018-02-15

2. Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans;Journal of Clinical Investigation;2017-03-27

3. Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L;The American Journal of Human Genetics;2016-06