A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutation.
about
Cell-surface processing of pro-ADAMTS9 by furinA disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif (ADAMTS) superfamily: functions and mechanismsFunctional evolution of ADAMTS genes: evidence from analyses of phylogeny and gene organizationADAMTS proteinases: a multi-domain, multi-functional family with roles in extracellular matrix turnover and arthritis.Discovery and characterization of a novel, widely expressed metalloprotease, ADAMTS10, and its proteolytic activationO-fucosylation of thrombospondin type 1 repeats in ADAMTS-like-1/punctin-1 regulates secretion: implications for the ADAMTS superfamilyADAMTS7B, the full-length product of the ADAMTS7 gene, is a chondroitin sulfate proteoglycan containing a mucin domainThe secreted metalloprotease ADAMTS20 is required for melanoblast survivalThe ADAMTS metalloproteinasesMolecular and developmental contributions to divergent pigment patterns in marine and freshwater sticklebacksA structural variant in the 5'-flanking region of the TWIST2 gene affects melanocyte development in belted cattleDetermination of Genetic Diversity among Korean Hanwoo Cattle Based on Physical CharacteristicsA customized pigmentation SNP array identifies a novel SNP associated with melanoma predisposition in the SLC45A2 gene.The multiple, complex roles of versican and its proteolytic turnover by ADAMTS proteases during embryogenesis.A new Adamts9 conditional mouse allele identifies its non-redundant role in interdigital web regression.The Roles of ADAMs Family Proteinases in Skin DiseasesGenome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate.ADAMTS9-Mediated Extracellular Matrix Dynamics Regulates Umbilical Cord Vascular Smooth Muscle Differentiation and RotationSpotlight on spotted mice: a review of white spotting mouse mutants and associated human pigmentation disorders.Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes.Epigenetic inactivation of the extracellular matrix metallopeptidase ADAMTS19 gene and the metastatic spread in colorectal cancer.Activation of beta-catenin signaling programs embryonic epidermis to hair follicle fate.Impaired ADAMTS9 secretion: A potential mechanism for eye defects in Peters Plus Syndrome.Stripes and belly-spots -- a review of pigment cell morphogenesis in vertebrates.ADAMTS metalloproteases generate active versican fragments that regulate interdigital web regression.Extracellular metalloproteinases in neural crest development and craniofacial morphogenesis.Regulation of ADAMTS9 secretion and enzymatic activity by its propeptide.Cooperation of two ADAMTS metalloproteases in closure of the mouse palate identifies a requirement for versican proteolysis in regulating palatal mesenchyme proliferation.Remapping of the belted phenotype in cattle on BTA3 identifies a multiplication event as the candidate causal mutation.ADAMTS9, a member of the ADAMTS family, in Xenopus development
P2860
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P2860
A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutation.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh-hant
name
A defect in a novel ADAMTS fam ...... elted white-spotting mutation.
@en
A defect in a novel ADAMTS fam ...... elted white-spotting mutation.
@nl
type
label
A defect in a novel ADAMTS fam ...... elted white-spotting mutation.
@en
A defect in a novel ADAMTS fam ...... elted white-spotting mutation.
@nl
prefLabel
A defect in a novel ADAMTS fam ...... elted white-spotting mutation.
@en
A defect in a novel ADAMTS fam ...... elted white-spotting mutation.
@nl
P2093
P356
P1433
P1476
A defect in a novel ADAMTS fam ...... elted white-spotting mutation.
@en
P2093
Cherie Rao
David R Beier
Dorothee Foernzler
Katherine A Jungers
Shanming Liu
Suneel S Apte
William J Pavan
P304
P356
10.1242/DEV.00668
P407
P577
2003-10-01T00:00:00Z