about
Down-regulation of ubiquitin ligase Cbl induced by twist haploinsufficiency in Saethre-Chotzen syndrome results in increased PI3K/Akt signaling and osteoblast proliferationIdentification of receptor and heparin binding sites in fibroblast growth factor 4 by structure-based mutagenesisGrowth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studiesHaim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin CA Genetic-Pathophysiological Framework for CraniosynostosisMetopic synostosisGenomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arraysTWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndromeGenomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosisCraniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndromeFGF18 is required for normal cell proliferation and differentiation during osteogenesis and chondrogenesisGli3Xt-J/Xt-J mice exhibit lambdoid suture craniosynostosis which results from altered osteoprogenitor proliferation and differentiationFGF9 regulates early hypertrophic chondrocyte differentiation and skeletal vascularization in the developing stylopodSox2 induction by FGF and FGFR2 activating mutations inhibits Wnt signaling and osteoblast differentiationDerivation of the mammalian skull vaultEvidence for digenic inheritance in some cases of Antley-Bixler syndrome?Presphenoidal synchondrosis fusion in DBA/2J mice.Hedgehog-dependent proliferation drives modular growth during morphogenesis of a dermal boneMutations in the human TWIST gene.The impact of molecular genetics on oral health paradigms.Adipose-derived stem cells: a review of signaling networks governing cell fate and regenerative potential in the context of craniofacial and long bone skeletal repair.Distinct Caenorhabditis elegans HLH-8/twist-containing dimers function in the mesoderm.Fibroblast growth factor signaling and basement membrane assembly are connected during epithelial morphogenesis of the embryoid bodyClinical findings in a patient with FGFR1 P252R mutation and comparison with the literature.The balance of WNT and FGF signaling influences mesenchymal stem cell fate during skeletal development.Mutations in fam20b and xylt1 reveal that cartilage matrix controls timing of endochondral ossification by inhibiting chondrocyte maturationCharacterization of distinct classes of differential gene expression in osteoblast cultures from non-syndromic craniosynostosis boneC. elegans twist gene expression in differentiated cell types is controlled by autoregulation through intron elementsThe BMP antagonist noggin regulates cranial suture fusion.The BMP ligand Gdf6 prevents differentiation of coronal suture mesenchyme in early cranial development.Phenotypic findings due to trisomy 7p15.3-pter including the TWIST locus.The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect.A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndromeRegulation of mandibular growth and morphogenesis.A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22.Molecular-pathogenetic classification of genetic disorders of the skeleton.A biochemist's guide to Caenorhabditis elegansMutations in snail family genes enhance craniosynostosis of Twist1 haplo-insufficient mice: implications for Saethre-Chotzen SyndromeA new method for generating point mutations in bacterial artificial chromosomes by homologous recombination in Escherichia coli.
P2860
Q24304940-989660FD-EF72-4146-963E-3F821B8ECA4BQ24550863-348F947C-B5A9-49E5-856F-54D1E1604614Q24675596-FB450176-5564-49DC-85AE-37100BBC2B79Q24681331-48930EAA-1DDA-4FE5-81C9-8C10D07D3596Q26784240-BA7E8D19-C6A0-4DB3-9A18-A5B3D3054176Q26823808-C67FE7E0-4AD0-4B0E-BD3F-26ED291C530AQ28294932-B5A08CCE-2730-4990-8886-5B2B2FD2B56FQ28296558-F1B2F189-1E10-484B-9F50-D4577FFA2E3FQ28344714-0E9706D5-507D-4F64-9308-76F84A072090Q28509010-7BA0A0D7-6610-4C95-83DB-916324A571A1Q28586991-E3B3422A-9D52-4F9C-95AD-D7A37C3AFF89Q28587566-D3AC0871-566F-4EE5-B84F-880276D44C6CQ28592971-F0C75272-BB07-43E0-B179-DC2D6E220D02Q28593870-55ACBB88-25D1-4AB4-B660-F0D7D2571050Q28767309-A836C3B5-7F0E-4AD0-BF0A-1A15AEF540C9Q30443021-00C9E52C-97B5-4728-9A9F-E14C515A1468Q30458724-06894CD3-E8DB-4A96-B15A-FFCEF57C0CCAQ30514571-08BD6A33-F5DE-45CD-A832-48B8FDE45762Q33825444-E5896F3D-0EFD-4C91-8AD6-9026D608DBABQ33842939-7378FA1E-3CB3-485D-A3F7-06A6C724FB2EQ33907462-E32F6958-472E-4A31-9E46-E2695D910223Q33915482-CD4401A0-AE4F-45DB-B0F6-88B8C9BB1A4BQ33946703-983DCB80-DA9D-48DE-B44E-C260642BD8FDQ33947191-F6546E9D-2961-40CA-85B8-2AF6F6D20B58Q33987011-B61B7400-155D-416A-87E5-780B053C03BBQ34013662-7BDC0B91-62EE-42EB-9341-BADC8296B8D5Q34112919-63211E0E-BCCC-4609-9041-53211422B82CQ34154831-BAE5648C-2690-4AA9-A77E-B121EB5E30C4Q34189687-DC7F69E9-273A-4B45-B267-EA1A35D78961Q34302263-A34F089F-D676-4E23-9526-E33ADB590206Q34373526-65BF3056-705A-4B59-9AD7-E7563599BB35Q34380582-B9CC0EB6-85B8-4B5A-B16E-54816E51D5A7Q34387671-1CA9638F-A890-4371-BE79-8E83A33964E3Q34388821-024B4635-7E6B-4047-841D-C0A3BA70C1F8Q34402686-3AD8B243-0147-4B7C-8B0B-5176D12BC66AQ34439719-A5614987-E36A-4EAB-98C6-60F34D93E103Q34561450-40479018-A165-4C24-A451-64CDE73BAA12Q34570449-637945D3-4B21-42AD-A099-34CB063EC25CQ34575381-3B398626-7F3B-4E36-8E69-364551FC754BQ34584758-195F2588-0F97-448A-9F9A-69A9C5C2E85D
P2860
description
1997 nî lūn-bûn
@nan
1997 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի հունվարին 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
Craniosynostosis: genes and mechanisms.
@ast
Craniosynostosis: genes and mechanisms.
@en
Craniosynostosis: genes and mechanisms.
@nl
type
label
Craniosynostosis: genes and mechanisms.
@ast
Craniosynostosis: genes and mechanisms.
@en
Craniosynostosis: genes and mechanisms.
@nl
prefLabel
Craniosynostosis: genes and mechanisms.
@ast
Craniosynostosis: genes and mechanisms.
@en
Craniosynostosis: genes and mechanisms.
@nl
P356
P1476
Craniosynostosis: genes and mechanisms.
@en
P304
P356
10.1093/HMG/6.10.1647
P577
1997-01-01T00:00:00Z