About: Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations

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description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) գիտական հոդված (hy) scholarly article (en) artículu científicu espublizáu en 2009 (ast) наукова стаття, опублікована в серпні 2009 (uk) 2009年學術文章 (zh) مقالة علمية نشرت في 24 أغسطس 2009 (ar)
publication date	wds:Q37340867-863320B7-CF0C-4A64-8855-32E3C5AB7BC6
publication date	2009-08-24 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37340867-6DB9F485-C70C-436E-B4C4-CFAEFDAEFAC7
language of work or name	English
cites work	wds:Q37340867-16F9B582-AEA4-46CC-8DF0-344B16AF8FF4 wds:Q37340867-235FC270-F328-4B21-B471-8A4AA5D86DA1 wds:Q37340867-2E963AFE-CBF4-4DBF-BAF5-CDCE2DEF19AD wds:Q37340867-44A25100-4A3E-4C63-8A4D-C21F7002D863 wds:Q37340867-48D52951-71DD-406A-94D0-3EE14D3533D5 wds:Q37340867-5B5F5518-87D7-498A-8495-7E96442C13CB wds:Q37340867-6D72F6FA-9B6F-4C5F-B090-E9B91BF116DB wds:Q37340867-6E21EAF1-3FD9-491F-B790-7B998614511A wds:Q37340867-7C9B4C68-DA24-4FEE-AA86-A70241A565A5 wds:Q37340867-7F1573A5-E94C-4CAC-84F1-591ABA8076E7 wds:Q37340867-892FA16E-08DC-4ED7-A4AE-627191A6DC49 wds:Q37340867-90C06807-6AA6-45D8-84EB-79EA8C05FF03 wds:Q37340867-96D7BC85-0DDD-4FF6-87CD-5282EE50ECB2 wds:Q37340867-9FCBC1E8-6085-43BE-B760-A954E3CF550C wds:Q37340867-B79F3E8B-31A8-4930-90BE-70BD4D8BF89E wds:Q37340867-B7B39A3D-7BAA-4674-93A7-0FE7CD3402AB wds:Q37340867-C4306A7D-5F7F-40E5-845E-D35C3A344A71 wds:Q37340867-C5A800C9-E9A8-452A-A37A-041976B0B8F5 wds:Q37340867-C88481C6-C234-4497-835D-FB12F9498986 wds:Q37340867-CA9B2405-D224-4BAD-A2F0-20B6E4666618 wds:Q37340867-CAA0412A-F8C5-4A23-ADEC-80E7B7BF4BF7 wds:Q37340867-D8C58E1C-E654-4623-B02E-62924CF471D6 wds:Q37340867-DBF6C4C5-6654-415F-B2D8-4E5E70D06D58 wds:Q37340867-DE2FE24D-25A0-424B-B0BB-9E214AEB55B8 wds:Q37340867-EA000403-90C2-4E66-A39B-6C08A0742FE0 wds:Q37340867-F95FD338-5AF0-4CD8-BCA0-14C774310126 wds:Q37340867-FE5D058D-8B46-4A78-818B-CD5787A54C3C
cites work	Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation Deletion of Ptpn11 (Shp2) in cardiomyocytes causes dilated cardiomyopathy via effects on the extracellular signal-regulated kinase/mitogen-activated protein kinase and RhoA signaling pathways Cis-acting regulatory sequences governing Wnt-1 expression in the developing mouse CNS Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences The tyrosine phosphatase Shp2 (PTPN11) in cancer. Craniofacial development: the tissue and molecular interactions that control development of the head Mechanisms of neural crest cell migration The duration, magnitude and compartmentalization of ERK MAP kinase activity: mechanisms for providing signaling specificity. Analysis of cranial neural crest cell migration and early fates in postimplantation rat chimaeras. Spatial and temporal patterns of ERK signaling during mouse embryogenesis Mediating ERK 1/2 signaling rescues congenital heart defects in a mouse model of Noonan syndrome Genetics of craniofacial development and malformation Role of ERK1/2 signaling in congenital valve malformations in Noonan syndrome Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity Tissue origins and interactions in the mammalian skull vault Regulation of growth factor signaling by FRS2 family docking/scaffold adaptor proteins The transcription factor MEF2C is required for craniofacial development Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome Noonan syndrome. An update and review for the primary pediatrician Recent advances in craniofacial morphogenesis Critical role of the extracellular signal-regulated kinase-MAPK pathway in osteoblast differentiation and skeletal development Molecular and cellular bases of syndromic craniosynostoses Cellular dynamics and tissue interactions of the dura mater during head development Ras-MAPK signaling in osteogenic differentiation: friend or foe?
author name string	wds:Q37340867-32AB3A4B-5CBA-4AB5-9992-DFF2181FB477 wds:Q37340867-38EEE62A-A83B-4ABA-9ACE-EFAB90A62FA2 wds:Q37340867-3FDD789E-9286-4890-AEB2-EE156E944227 wds:Q37340867-F0F24A8A-B34A-4EEE-8025-EC79561AD6CC
author name string	Tomoki Nakamura Jeffrey Robbins James Gulick Ronald Pratt
rdfs:label	Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations (en) Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations (nl) Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations (ast)
skos:prefLabel	Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations (en) Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations (nl) Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations (ast)
name	Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations (en) Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations (nl) Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations (ast)
title	wds:Q37340867-4EB7BD83-68FE-423F-8DEE-B9F877530CB1
title	Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations (en)
page(s)	wds:Q37340867-C00AF5AA-089C-47A2-9924-912F0563B6BE
page(s)	15436-15441
instance of	wds:Q37340867-D137402B-6F8A-462B-8287-A6E6B9A1C159
instance of	scholarly article

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