Targeted disruption of the Mn1 oncogene results in severe defects in development of membranous bones of the cranial skeleton.
about
MN1, a novel player in human AMLMolecular basis of cleft palates in miceThe vitamin D receptor (VDR) gene polymorphisms in Turkish brain cancer patientsChromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate.Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibromatosis 2 (NF2): a case report and review of the literature.Sulfonation chemistry as a powerful tool for MALDI TOF/TOF de novo sequencing and post-translational modification analysis.Forging links between human mental retardation-associated CNVs and mouse gene knockout models.Molecular Targets and Treatment of Meningioma.Mapping of MN1 sequences necessary for myeloid transformation.Mapping of Craniofacial Traits in Outbred Mice Identifies Major Developmental Genes Involved in Shape DeterminationDiagnostic and molecular pathology of meningiomas.The Mn1 transcription factor acts upstream of Tbx22 and preferentially regulates posterior palate growth in mice.Meningioma 1 is required for appropriate osteoblast proliferation, motility, differentiation, and function.The Ptch1(DL) mouse: a new model to study lambdoid craniosynostosis and basal cell nevus syndrome-associated skeletal defects.Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing.Analysis of human soft palate morphogenesis supports regional regulation of palatal fusion.The Meningioma 1 (MN1) Gene is an Independent Poor Prognostic Factor in Adult Egyptian Acute Myeloid Leukemia PatientsRegional DNA methylation differences between humans and chimpanzees are associated with genetic changes, transcriptional divergence and disease genes.Craniofacial abnormalities and developmental delay in two families with overlapping 22q12.1 microdeletions involving the MN1 gene.Creating diversity in mammalian facial morphology: a review of potential developmental mechanisms.
P2860
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P2860
Targeted disruption of the Mn1 oncogene results in severe defects in development of membranous bones of the cranial skeleton.
description
2005 nî lūn-bûn
@nan
2005 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Targeted disruption of the Mn1 ...... bones of the cranial skeleton
@nl
Targeted disruption of the Mn1 ...... bones of the cranial skeleton.
@ast
Targeted disruption of the Mn1 ...... bones of the cranial skeleton.
@en
type
label
Targeted disruption of the Mn1 ...... bones of the cranial skeleton
@nl
Targeted disruption of the Mn1 ...... bones of the cranial skeleton.
@ast
Targeted disruption of the Mn1 ...... bones of the cranial skeleton.
@en
prefLabel
Targeted disruption of the Mn1 ...... bones of the cranial skeleton
@nl
Targeted disruption of the Mn1 ...... bones of the cranial skeleton.
@ast
Targeted disruption of the Mn1 ...... bones of the cranial skeleton.
@en
P2093
P2860
P1476
Targeted disruption of the Mn1 ...... bones of the cranial skeleton
@en
P2093
Anco C Molijn
Arnold C P Hekman
Christl Vermey-Keers
Ellen C Zwarthoff
Magda A Meester-Smoor
Marcel Vermeij
Marjolein J L van Helmond
Peter H J Riegman
P2860
P304
P356
10.1128/MCB.25.10.4229-4236.2005
P407
P577
2005-05-01T00:00:00Z