Comprehensive genetic analysis of overlapping syndromes of RAS/RAF/MEK/ERK pathway-Reference-Cited by-同舟云学术

Comprehensive genetic analysis of overlapping syndromes of RAS/RAF/MEK/ERK pathway

Published:2009-12-17 Issue:4 Volume:52 Page:557-562
ISSN:1328-8067
Container-title:Pediatrics International
language:en
Short-container-title:

Author:

Tumurkhuu Munkhtuya,Saitoh Makiko,Sato Atsushi,Takahashi Kan,Mimaki Masakazu,Takita Junko,Takeshita Kazuhide,Hama Takehiro,Oka Akira,Mizuguchi Masashi

Publisher

Wiley

Subject

Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.2009.03020.x/fullpdf

Reference32 articles.

1. Stops along the RAS pathway in human genetic disease;Alj;Nat. Med.,2006

2. RAS oncogenes: The first 30 years;Malumbres;Nat. Rev. Cancer,2003

3. Germline mutations in HRAS proto-oncogene cause Costello syndrome;Aoki;Nat. Genet.,2005

4. Ras oncogenes in human cancer (a review);Bos;Cancer Res.,1989

5. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome;Tartaglia;Nat. Genet.,2001

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2. A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation;Genetics Research;2019

3. Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome;BMC Pediatrics;2018-08-29

4. The RASopathy Family: Consequences of Germline Activation of the RAS/MAPK Pathway;Endocrine Reviews;2018-06-18

5. The novel RAF1 mutation p.(Gly361Ala) located outside the kinase domain of the CR3 region in two patients with Noonan syndrome, including one with a rare brain tumor;American Journal of Medical Genetics Part A;2017-12-22