The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic cases
about
Normal and disease-related biological functions of Twist1 and underlying molecular mechanismsCraniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndromeA newly described bovine type 2 scurs syndrome segregates with a frame-shift mutation in TWIST1The impact of genomic neighborhood on the evolution of human and chimpanzee transcriptome.Destabilization of the TWIST1/E12 complex dimerization following the R154P point-mutation of TWIST1: an in silico approach.Phenotypic findings due to trisomy 7p15.3-pter including the TWIST locus.A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.Mutations in snail family genes enhance craniosynostosis of Twist1 haplo-insufficient mice: implications for Saethre-Chotzen SyndromeTwist1 controls a cell-specification switch governing cell fate decisions within the cardiac neural crestConserved non-genic sequences - an unexpected feature of mammalian genomes.Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis.Understanding craniosynostosis as a growth disorderDeciphering the molecular mechanisms underlying the binding of the TWIST1/E12 complex to regulatory E-box sequences.Inducible knockout of Twist1 in young and adult mice prolongs hair growth cycle and has mild effects on general health, supporting Twist1 as a preferential cancer targetReoperation for intracranial hypertension in TWIST1-confirmed Saethre-Chotzen syndrome: a 15-year review.Molecular dissection of germline chromothripsis in a developmental context using patient-derived iPS cells.Multiple biological functions of Twist1 in various cancers.Common regulation of growth arrest and differentiation of osteoblasts by helix-loop-helix factors.Twist1 contributes to cranial bone initiation and dermal condensation by maintaining Wnt signaling responsiveness.
P2860
Q26824524-77F02746-AD6E-4BC6-B537-4031ED2381E3Q28509010-B2E46809-B307-4F3F-A8C4-A0C44BCD3AC3Q28742339-943C7D42-017F-40B6-9BFC-CE812012457FQ33411222-DEA714C1-ECE8-495B-8B15-AAFBDE0A91A2Q33706887-8411F4CD-0AF9-4AFD-AB09-234332FF9BB1Q34373526-4104EF28-1607-4F05-8326-3BF88F311C7EQ34387671-ACDF4F49-ABF8-43E3-8515-AA8C8761FAD0Q34575381-FFF14A59-B3D6-48C5-89B6-94D2FE01203CQ34650000-DAED54D3-4B52-4D49-9D05-2E6C2E14669CQ36045183-9F0F9234-D5BE-438D-AA17-BC09EE8BBC35Q36629781-1296DBE4-98E6-45DF-A4E5-135C10807ED2Q37014071-EE75F3AB-9E81-406B-B14D-22652EEC6A32Q37021574-367AF5BE-F4DF-42ED-A6EF-32C1BC9527D8Q37218775-806CE294-32E1-4243-8CAA-0C93E30EAF12Q37284855-03100CF9-55B4-4223-9F9B-BEAD0EB4BC29Q37609839-7AFD3518-B308-4FC2-9684-DFB604859359Q37746336-8D861F63-E7A7-407F-B72A-8D28212E34EBQ39528734-8860A382-EAB4-4908-97A2-A7F94ED46BB3Q42685028-EFFBA20B-6B4A-49D8-8697-3713417FB0BA
P2860
The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic cases
description
1997 nî lūn-bûn
@nan
1997 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
The TWIST gene, although not d ...... in familial and sporadic cases
@ast
The TWIST gene, although not d ...... in familial and sporadic cases
@en
The TWIST gene, although not d ...... in familial and sporadic cases
@nl
type
label
The TWIST gene, although not d ...... in familial and sporadic cases
@ast
The TWIST gene, although not d ...... in familial and sporadic cases
@en
The TWIST gene, although not d ...... in familial and sporadic cases
@nl
prefLabel
The TWIST gene, although not d ...... in familial and sporadic cases
@ast
The TWIST gene, although not d ...... in familial and sporadic cases
@en
The TWIST gene, although not d ...... in familial and sporadic cases
@nl
P2093
P3181
P356
P1476
The TWIST gene, although not d ...... in familial and sporadic cases
@en
P2093
P304
P3181
P356
10.1093/HMG/6.8.1369
P407
P577
1997-08-01T00:00:00Z