about
The MAPK pathway across different malignancies: a new perspective.Legius syndrome in fourteen families.Observations on intelligence and behavior in 15 patients with Legius syndromePediatric 25-hydroxyvitamin D concentrations in neurofibromatosis type 1The SPRED1 Variants Repository for Legius SyndromeInteraction between a Domain of the Negative Regulator of the Ras-ERK Pathway, SPRED1 Protein, and the GTPase-activating Protein-related Domain of Neurofibromin Is Implicated in Legius Syndrome and Neurofibromatosis Type 1.The musculoskeletal phenotype of the RASopathies.Review and update of SPRED1 mutations causing Legius syndrome.Differential gene expression of the key signalling pathway in para-carcinoma, carcinoma and relapse human pancreatic cancer.A shared molecular mechanism underlies the human rasopathies Legius syndrome and Neurofibromatosis-1.Identification of SPRED1 deletions using RT-PCR, multiplex ligation-dependent probe amplification and quantitative PCR.
P2860
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P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
SPRED 1 mutations in a neurofibromatosis clinic
@ast
SPRED 1 mutations in a neurofibromatosis clinic
@en
SPRED 1 mutations in a neurofibromatosis clinic
@nl
type
label
SPRED 1 mutations in a neurofibromatosis clinic
@ast
SPRED 1 mutations in a neurofibromatosis clinic
@en
SPRED 1 mutations in a neurofibromatosis clinic
@nl
prefLabel
SPRED 1 mutations in a neurofibromatosis clinic
@ast
SPRED 1 mutations in a neurofibromatosis clinic
@en
SPRED 1 mutations in a neurofibromatosis clinic
@nl
P2093
P2860
P356
P1476
SPRED 1 mutations in a neurofibromatosis clinic
@en
P2093
David A Stevenson
David C Dries
David H Viskochil
Talia M Muram-Zborovski
P2860
P304
P356
10.1177/0883073809359540
P407
P577
2010-10-01T00:00:00Z