A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome-Reference-Cited by-同舟云学术

A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome

Published:2004-03-21 Issue:4 Volume:36 Page:339-341
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Mnatzakanian Gevork N,Lohi Hannes,Munteanu Iulia,Alfred Simon E,Yamada Takahiro,MacLeod Patrick J M,Jones Julie R,Scherer Stephen W,Schanen N Carolyn,Friez Michael J,Vincent John B,Minassian Berge A

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1327.pdf

Reference13 articles.

1. Hagberg, B. Ment. Retard. Dev. Disabil. Res. Rev. 8, 61–65 (2002).

2. Amir, R.E. et al. Nat. Genet. 23, 185–188 (1999).

3. Miltenberger-Miltenyi, G. & Laccone, F. Hum. Mutat. 22, 107–115 (2003).

4. Reichwald, K. et al. Mamm. Genome. 11, 182–190 (2000).

5. Schouten, J.P. et al. Nucleic Acids Res. 30, e57 (2002).

Cited by 278 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. MeCP2 is a naturally supercharged protein with cell membrane transduction capabilities;Protein Science;2024-09-14

2. Testing the PEST hypothesis using relevant Rett mutations in MeCP2 E1 and E2 isoforms;Human Molecular Genetics;2024-08-14

3. Heterozygous ZNHIT3 variants within the 17q12 recurrent deletion region are associated with Mayer-Rokitansky-Kuster Hauser (MRKH) syndrome;Molecular and Cellular Endocrinology;2024-08

4. Epigenetics in rare neurological diseases;Frontiers in Cell and Developmental Biology;2024-07-23

5. Systematic and quantitative analysis of stop codon readthrough in Rett syndrome nonsense mutations;Journal of Molecular Medicine;2024-03-02