相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Mitochondrial dysfunction and organic aciduria in five patients carrying mutations in the Ras-MAPK pathway
Tjitske Kleefstra et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2011)
Excess of Neuromuscular Spindles in a Fetus with Costello Syndrome: A Clinicopathological Report
Martine Sinico et al.
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY (2011)
Congenital myopathies - a comprehensive update of recent advancements
M. C. Sharma et al.
ACTA NEUROLOGICA SCANDINAVICA (2009)
Different roles of H-ras for regulation of myosin heavy chain promoters in satellite cell-derived muscle cell culture during proliferation and differentiation
Michael E. Scholz et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2009)
MEK1 plays contrary stage-specific roles in skeletal myogenic differentiation
Chulman Jo et al.
CELLULAR SIGNALLING (2009)
The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulation
William E. Tidyman et al.
CURRENT OPINION IN GENETICS & DEVELOPMENT (2009)
Kinase-activating and kinase-impaired cardio-facio-cutaneous syndrome alleles have activity during zebrafish development and are sensitive to small molecule inhibitors
Corina Anastasaki et al.
HUMAN MOLECULAR GENETICS (2009)
Modulation of skeletal muscle fiber type by mitogen-activated protein kinase signaling
Hao Shi et al.
FASEB JOURNAL (2008)
Neurological complications of cardio-facio-cutaneous syndrome
Grace Yoon et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2007)
Myopathy caused by HRAS germline mutations:: implications for disturbed myogenic differentiation in the presence of constitutive HRas activation
Ineke van der Burgt et al.
JOURNAL OF MEDICAL GENETICS (2007)
Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome
P Rodriguez-Viciana et al.
SCIENCE (2006)
HRAS mutations in Costello syndrome: Detection of constitutional activating mutations in codon 12 and 13 and loss of wild-type allele in malignancy
AL Estep et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
Actin mutations are one cause of congenital fibre type disproportion
NG Laing et al.
ANNALS OF NEUROLOGY (2004)
Activated MEK1 binds the nuclear MyoD transcriptional complex to repress transactivation
RLS Perry et al.
MOLECULAR CELL (2001)
Ras is involved in nerve-activity-dependent regulation of muscle genes
M Murgia et al.
NATURE CELL BIOLOGY (2000)
分享论文
