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Down-regulation of ubiquitin ligase Cbl induced by twist haploinsufficiency in Saethre-Chotzen syndrome results in increased PI3K/Akt signaling and osteoblast proliferationHOXA5-twist interaction alters p53 homeostasis in breast cancer cellsAltered Twist1 and Hand2 dimerization is associated with Saethre-Chotzen syndrome and limb abnormalitiesNormal and disease-related biological functions of Twist1 and underlying molecular mechanismsFunctional Analysis of Two Novel Mutations in TWIST1 Protein Motifs Found in Ventricular Septal Defect PatientsA survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individualsAnother TWIST on Baller-Gerold syndromeSaethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndromeA newly described bovine type 2 scurs syndrome segregates with a frame-shift mutation in TWIST1Presphenoidal synchondrosis fusion in DBA/2J mice.Heterozygous disruption of the TATA-binding protein gene in DT40 cells causes reduced cdc25B phosphatase expression and delayed mitosis.Computational modeling of the bHLH domain of the transcription factor TWIST1 and R118C, S144R and K145E mutantsTWIST1 associates with NF-κB subunit RELA via carboxyl-terminal WR domain to promote cell autonomous invasion through IL8 productionSignaling pathways in osteogenesis and osteoclastogenesis: Lessons from cranial sutures and applications to regenerative medicine.Syndromic craniosynostosis: from history to hydrogen bonds.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 targetA twist of insight - the role of Twist-family bHLH factors in development.PKB/AKT phosphorylation of the transcription factor Twist-1 at Ser42 inhibits p53 activity in response to DNA damage.Severe persistent pulmonary hypertension of the newborn and dysmorphic features in neonate with a deletion involving TWIST1 and PHF14: a case report.Saethre-Chotzen syndrome: a case report.Saethre–Chotzen syndrome with an atypical phenotype: identification of TWIST microdeletion by array CGH.Saethre-Chotzen syndrome, Pro136His TWIST mutation, hearing loss, and external and middle ear structural anomalies: report on a Brazilian family.Genetic analysis of patients with the Saethre-Chotzen phenotype.Second family with the Boston-type craniosynostosis syndrome: novel mutation and expansion of the clinical spectrum.Saethre-Chotzen syndrome: notable intrafamilial phenotypic variability in a large family with Q28X TWIST mutationUnilateral coronal synostosis: a histomorphometric study
P2860
Q24304940-DB885448-CEE5-4241-93EE-67978226ECCCQ24315091-56223A7D-B37E-4107-A045-E81DBBDB0C33Q24651500-63232905-CF3A-456C-B6DD-A1526CE61FDBQ26824524-C318969A-8E81-4E45-AC28-13DE481D2D64Q28115006-FFA4F93E-BB22-4701-8461-2BD6F7AE3C8EQ28211953-02B49952-A15C-4E62-95EB-1BF51868E415Q28213315-E96C19F4-5923-4E1F-91BC-0CA9B08258DDQ28279180-4DEB67B7-70F3-4365-A08B-FFE1153CE9C2Q28742339-3FC6C79D-E789-47ED-A708-1F471CF58E1CQ30458724-B52E03B2-0421-4B23-8FEA-536A32DBE9E3Q33967804-63115F05-F5FB-44DD-BD49-EB359ED8B9CBQ34354239-92900EBC-0592-4738-904D-9E0039B9A55BQ34379330-91301026-4BDD-413E-9970-377AE70A5AD5Q35587493-69048C7B-B073-4EAA-8F14-62680EE18108Q36841903-8EB3FE7F-31F4-464A-A257-7B28765FD223Q37218775-872BC184-6ED7-4AC6-B711-7DE61399868DQ37332873-CE096AF6-8B29-4D25-9906-F324C78D7920Q39713494-A3F3FCBB-265E-4A7F-AA16-6574F4E2C85FQ41438938-0646BE2B-DD64-48F9-A8F5-C2DBE73CFC31Q46909092-E1CB709D-322B-4D73-94A7-F1209DE1515AQ47745464-F915F365-5047-461B-96AC-FBC780212F55Q48293575-EB4794A5-026A-43A9-B1CB-F89D1F38CED5Q52117348-E7D2B260-E924-4DD0-943D-F76B37C7197DQ53099238-E799A07E-E3CF-4C3A-8EC1-5D3115169713Q55670711-C9095C84-8E3C-4BE3-922D-798A8E2ECAFBQ56346736-7FEED040-DE57-4671-A09D-1E8D97EE3C2B
P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Mutations in the human TWIST gene.
@ast
Mutations in the human TWIST gene.
@en
type
label
Mutations in the human TWIST gene.
@ast
Mutations in the human TWIST gene.
@en
prefLabel
Mutations in the human TWIST gene.
@ast
Mutations in the human TWIST gene.
@en
P2093
P2860
P1433
P1476
Mutations in the human TWIST gene.
@en
P2093
P2860
P304
P356
10.1002/(SICI)1098-1004(200002)15:2<150::AID-HUMU3>3.0.CO;2-D
P577
2000-01-01T00:00:00Z