Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
about
Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).OC-2, a novel mammalian member of the ONECUT class of homeodomain transcription factors whose function in liver partially overlaps with that of hepatocyte nuclear factor-6Regulation of number and size of digits by posterior Hox genes: A dose-dependent mechanism with potential evolutionary implicationsSynpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tractSHOT, a SHOX-related homeobox gene, is implicated in craniofacial, brain, heart, and limb developmentThe HOXC11 homeodomain protein interacts with the lactase-phlorizin hydrolase promoter and stimulates HNF1alpha-dependent transcriptionBardet-Biedl syndrome: a molecular and phenotypic study of 18 familiesOver- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarismNovel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndromeLocalization of a gene for syndactyly type 1 to chromosome 2q34-q36.Localization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22.Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated families.Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD clusterTranscription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiencyA 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactylyMutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndromeDevelopmental rescue of Drosophila cephalic defects by the human Otx genesA systematic review of association studies of common variants associated with idiopathic congenital talipes equinovarus (ICTEV) in humans in the past 30 yearsMutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese familiesAmegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutationHuman HOX gene mutationsComplete mutation analysis panel of the 39 human HOX genesHnRNP A1 and A/B interaction with PABPN1 in oculopharyngeal muscular dystrophyLimb malformations and the human HOX genesDistinct global shifts in genomic binding profiles of limb malformation-associated HOXD13 mutationsEvolutionary trajectories of snake genes and genomes revealed by comparative analyses of five-pacer viperTandem amino acid repeats in the green anole (Anolis carolinensis) and other squamates may have a role in increasing genetic variabilityBone developmentThe origin of the Australasian marsupial fauna and the phylogenetic affinities of the enigmatic monito del monte and marsupial moleIdentification of an optimal Ncx binding sequence required for transcriptional activationEngineering of an elastic scaffolding polyprotein based on an SH3-binding intrinsically disordered titin PEVK module.Comparative phylogenomic analyses of teleost fish Hox gene clusters: lessons from the cichlid fish Astatotilapia burtoni.Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences.Congenital thrombocytopenia and radio-ulnar synostosis: a new familial syndrome.Reconstructing the history of human limb development: lessons from birth defects.Cleidocranial dysplasia: clinical and molecular genetics.Transcription factors in dysmorphology.First report of CFTR mutations in black cystic fibrosis patients of southern African originMesoaxial complete syndactyly and synostosis with hypoplastic thumbs: an unusual combination or homozygous expression of syndactyly type I?Comparative analyses of vertebrate posterior HoxD clusters reveal atypical cluster architecture in the caecilian Typhlonectes natans
P2860
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P2860
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
description
1996 nî lūn-bûn
@nan
1996 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
@ast
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
@en
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
@en-gb
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
@nl
type
label
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
@ast
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
@en
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
@en-gb
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
@nl
prefLabel
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
@ast
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
@en
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
@en-gb
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
@nl
P2093
P3181
P1433
P1476
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
@en
P2093
P304
P3181
P356
10.1126/SCIENCE.272.5261.548
P407
P577
1996-04-26T00:00:00Z