Compound mutants for the paralogous hoxa-4, hoxb-4, and hoxd-4 genes show more complete homeotic transformations and a dose-dependent increase in the number of vertebrae transformed
about
Regulation of number and size of digits by posterior Hox genes: A dose-dependent mechanism with potential evolutionary implicationsCdx1 autoregulation is governed by a novel Cdx1-LEF1 transcription complexThe evolution of the vertebrate Dlx gene familyA genomic approach to the identification and characterization of HOXA13 functional binding elementsTALE transcription factors during early development of the vertebrate brain and eyeHox genes and limb musculoskeletal developmentZebrafish hoxd4a acts upstream of meis1.1 to direct vasculogenesis, angiogenesis and hematopoiesisComplete mutation analysis panel of the 39 human HOX genesMice lacking the ski proto-oncogene have defects in neurulation, craniofacial, patterning, and skeletal muscle developmentHox11 paralogous genes are essential for metanephric kidney inductionDefective neural tube closure and anteroposterior patterning in mice lacking the LIM protein LMO4 or its interacting partner Deaf-1Selection on different genes with equivalent functions: the convergence story told by Hox genes along the evolution of aquatic mammalian lineagesGlobal posterior prevalence is unique to vertebrates: a dance to the music of time?Additional sex combs-like 1 belongs to the enhancer of trithorax and polycomb group and genetically interacts with Cbx2 in miceMolecular genetics of tooth morphogenesis and patterning: the right shape in the right place.Correlation between Hox code and vertebral morphology in the mouse: towards a universal model for SynapsidaGeneration and expression of a Hoxa11eGFP targeted allele in mice.Complementation mapping of skeletal and central nervous system abnormalities in mice of the piebald deletion complexNuclear accumulation of an uncapped RNA produced by Drosha cleavage of a transcript encoding miR-10b and HOXD4Genome engineering via homologous recombination in mouse embryonic stem (ES) cells: an amazingly versatile tool for the study of mammalian biology.Posterior Hox gene expression in developing genitalia.Opposite phenotypes of hypomorphic and Y766 phosphorylation site mutations reveal a function for Fgfr1 in anteroposterior patterning of mouse embryosRostral and caudal pharyngeal arches share a common neural crest ground patternHox genes regulate the onset of Tbx5 expression in the forelimb.Evidence for regulation of cartilage differentiation by the homeobox gene Hoxc-8.Mesenchymal Hox6 function is required for mouse pancreatic endocrine cell differentiation.Retardation of skeletal development and cervical abnormalities in transgenic mice expressing a dominant-negative retinoic acid receptor in chondrogenic cells.Molecular basis for skeletal variation: insights from developmental genetic studies in mice.Ash1l methylates Lys36 of histone H3 independently of transcriptional elongation to counteract polycomb silencingMorpholino-mediated knockdown in primary chondrocytes implicates Hoxc8 in regulation of cell cycle progression.Transgenic studies on homeobox genes in nervous system development: spina bifida in Isl1 transgenic miceEstablishment of Hox vertebral identities in the embryonic spine precursorsHox genes and regional patterning of the vertebrate body plan.Hox genes and kidney development.Large-scale mouse knockouts and phenotypes.The dual roles of homeobox genes in vascularization and wound healing.Controlling Hox gene expression and activity to build the vertebrate axial skeleton.The Role of Hox Genes in Female Reproductive Tract Development, Adult Function, and Fertility.The role of HOX genes in head and neck squamous cell carcinoma.Hox11 Function Is Required for Region-Specific Fracture Repair.
P2860
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P2860
Compound mutants for the paralogous hoxa-4, hoxb-4, and hoxd-4 genes show more complete homeotic transformations and a dose-dependent increase in the number of vertebrae transformed
description
1995 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1995
@ast
im Juli 1995 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1995/07/01)
@sk
vědecký článek publikovaný v roce 1995
@cs
wetenschappelijk artikel (gepubliceerd op 1995/07/01)
@nl
наукова стаття, опублікована в липні 1995
@uk
مقالة علمية (نشرت في يوليو 1995)
@ar
name
Compound mutants for the paral ...... umber of vertebrae transformed
@ast
Compound mutants for the paral ...... umber of vertebrae transformed
@en
Compound mutants for the paral ...... umber of vertebrae transformed
@nl
type
label
Compound mutants for the paral ...... umber of vertebrae transformed
@ast
Compound mutants for the paral ...... umber of vertebrae transformed
@en
Compound mutants for the paral ...... umber of vertebrae transformed
@nl
prefLabel
Compound mutants for the paral ...... umber of vertebrae transformed
@ast
Compound mutants for the paral ...... umber of vertebrae transformed
@en
Compound mutants for the paral ...... umber of vertebrae transformed
@nl
P2093
P921
P3181
P356
P1433
P1476
Compound mutants for the paral ...... umber of vertebrae transformed
@en
P2093
D J Wolgemuth
R R Behringer
R Ramírez-Solis
P304
P3181
P356
10.1101/GAD.9.13.1667
P577
1995-07-01T00:00:00Z