Disruption of formin-encoding transcripts in two mutant limb deformity alleles.
about
The human formin-binding protein 17 (FBP17) interacts with sorting nexin, SNX2, and is an MLL-fusion partner in acute myelogeneous leukemiaA human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterilityYeast studies reveal moonlighting functions of the ancient actin cytoskeletonFormins at a glanceThe formin/diaphanous-related protein, FHOS, interacts with Rac1 and activates transcription from the serum response elementMolecular interaction between limb deformity proteins (formins) and Src family kinasesGenetic evidence that formins function within the nucleusMammalian formin-1 participates in adherens junctions and polymerization of linear actin cablesFormin 1-isoform IV deficient cells exhibit defects in cell spreading and focal adhesion formationDeficient outgrowth of the ureteric bud underlies the renal agenesis phenotype in mice manifesting the limb deformity (ld) mutationFormin1 mediates the induction of dendritogenesis and synaptogenesis by neurogenin3 in mouse hippocampal neuronsMouse limb deformity mutations disrupt a global control region within the large regulatory landscape required for Gremlin expressionFormins in development: orchestrating body plan origami.Genomic identification of regulatory elements by evolutionary sequence comparison and functional analysisLong-range control of gene expression: emerging mechanisms and disruption in disease.Interdependence of filamentous actin and microtubules for asymmetric cell division.Gremlin - a putative pathogenic player in progressive renal disease.A human gene homologous to the formin gene residing at the murine limb deformity locus: chromosomal location and RFLPsFormin1 disruption confers oligodactylism and alters Bmp signaling.Wattles in goats are associated with the FMN1/GREM1 region on chromosome 10.Limb deformity proteins during avian neurulation and sense organ development
P2860
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P2860
Disruption of formin-encoding transcripts in two mutant limb deformity alleles.
description
1990 nî lūn-bûn
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1990年の論文
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1990年学术文章
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1990年学术文章
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1990年学术文章
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1990年学术文章
@zh-my
1990年学术文章
@zh-sg
1990年學術文章
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1990年學術文章
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1990年學術文章
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name
Disruption of formin-encoding transcripts in two mutant limb deformity alleles.
@en
type
label
Disruption of formin-encoding transcripts in two mutant limb deformity alleles.
@en
prefLabel
Disruption of formin-encoding transcripts in two mutant limb deformity alleles.
@en
P2093
P356
P1433
P1476
Disruption of formin-encoding transcripts in two mutant limb deformity alleles.
@en
P2093
P2888
P304
P356
10.1038/346853A0
P407
P577
1990-08-01T00:00:00Z
P6179
1042804992