Transcriptional hallmarks of noonan syndrome and noonan-like syndrome with loose anagen hair
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Transcriptional hallmarks of noonan syndrome and noonan-like syndrome with loose anagen hair
Authors
Keywords
-
Journal
HUMAN MUTATION
Volume 33, Issue 4, Pages 703-709
Publisher
Wiley
Online
2012-01-18
DOI
10.1002/humu.22026
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Noonan syndrome and clinically related disorders
- (2011) Marco Tartaglia et al. BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
- Heterozygous Germline Mutations in the CBL Tumor-Suppressor Gene Cause a Noonan Syndrome-like Phenotype
- (2010) Simone Martinelli et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Disorders of dysregulated signal traffic through the RAS-MAPK pathway: phenotypic spectrum and molecular mechanisms
- (2010) Marco Tartaglia et al. Annals of the New York Academy of Sciences
- The Scaffold Protein Shoc2/SUR-8 Accelerates the Interaction of Ras and Raf
- (2010) Rie Matsunaga-Udagawa et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia
- (2010) B. Perez et al. JOURNAL OF MEDICAL GENETICS
- Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia
- (2010) Charlotte M Niemeyer et al. NATURE GENETICS
- Growth Factor Independence 1 Protects Hematopoietic Stem Cells Against Apoptosis but Also Prevents the Development of a Myeloproliferative-Like Disease
- (2010) Cyrus Khandanpour et al. STEM CELLS
- KEA: kinase enrichment analysis
- (2009) A. Lachmann et al. BIOINFORMATICS
- Transcriptional Control of Pacemaker Channel Genes HCN2 and HCN4 by Sp1 and Implications in Re-expression of These Genes in Hypertrophied Myocytes
- (2009) Huixian Lin et al. CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
- The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulation
- (2009) William E Tidyman et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- Bilateral cochlear implantation in children with Noonan syndrome
- (2009) C. Scheiber et al. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY
- An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice
- (2009) Morag A Lewis et al. NATURE GENETICS
- Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair
- (2009) Viviana Cordeddu et al. NATURE GENETICS
- Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
- (2009) Da Wei Huang et al. Nature Protocols
- The tyrosine phosphatase Shp2 (PTPN11) directs Neuregulin-1/ErbB signaling throughout Schwann cell development
- (2009) K. S. Grossmann et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Protein tyrosine phosphatases in the JAK/STAT pathway
- (2008) Dan Xu Frontiers in Bioscience-Landmark
- M-CSF Signals through the MAPK/ERK Pathway via Sp1 to Induce VEGF Production and Induces Angiogenesis In Vivo
- (2008) Jennifer M. Curry et al. PLoS One
- The molecular functions of Shp2 in the Ras/Mitogen-activated protein kinase (ERK1/2) pathway
- (2007) Marie Dance et al. CELLULAR SIGNALLING
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search