About: skeletal system development

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

process whose specific outcome is the progression of the skeleton over time, from its formation to the mature structure

Attributes	Values
rdf:type	Item
description	biologisch proces (nl) біологічний процес (uk) process whose specific outcome is the progression of the skeleton over time, from its formation to the mature structure (en) skeletal system (gu)
exact match	wds:Q14860466-B88F23D8-2AE8-439F-A62B-F0ED97CA5F34
exact match	http://purl.obolibrary.org/obo/GO_0001501
rdfs:label	desarrollo del esqueleto (es) disvolvo de skeleta sistemo (eo) razvoj okostja (sl) skeletal system development (en) utvikling av skjelettsystem (nn) התפתחות השלד (he) 骨格系発生 (ja) 骨骼系统的发生 (zh) 骨骼系统的发生 (zh-cn)
skos:prefLabel	desarrollo del esqueleto (es) disvolvo de skeleta sistemo (eo) razvoj okostja (sl) skeletal system development (en) utvikling av skjelettsystem (nn) התפתחות השלד (he) 骨格系発生 (ja) 骨骼系统的发生 (zh) 骨骼系统的发生 (zh-cn)
name	desarrollo del esqueleto (es) disvolvo de skeleta sistemo (eo) razvoj okostja (sl) skeletal system development (en) utvikling av skjelettsystem (nn) התפתחות השלד (he) 骨格系発生 (ja) 骨骼系统的发生 (zh) 骨骼系统的发生 (zh-cn)
Gene Ontology ID	wds:Q14860466-10011969-85C3-4C15-8BB4-A9531A4C919D
Gene Ontology ID	GO:0001501
instance of	wds:Q14860466-01CEB37A-62ED-4548-B222-68FCFF627526
instance of	biological process
subclass of	wds:Q14860466-800F702E-1A3D-4455-A5E2-D12A72D525D5
subclass of	organism system development
anatomical location	wds:Q14860466-9de795a8-477f-51a9-ae9a-dbcfa6059e50
anatomical location	skeleton
skos:altLabel	GO:0001501 (en) GO:0001501 (nn) bhavik (gu) desarrollo esqueletal (es) razvoj skeleta (sl) razvoj skeletnega sistema (sl) skeletal development (en) skjelettutvikling (nn)
Encyclopedia of China (Third Edition) ID	wds:Q14860466-5E50F99E-0004-4A29-BFBC-3AA59D3B0DF1
UMLS CUI	wds:Q14860466-4559B0CA-ECFC-4153-A5CE-C17BFE3887EA
JSTOR topic ID	wds:Q14860466-471E97BE-EED7-4583-9D0B-B7F254BB6593
Encyclopedia of China (Third Edition) ID	107475
UMLS CUI	C1160401
JSTOR topic ID	skeletal-development
is field of work of	Paul O'Higgins
is field of work of	wds:Q30004269-40b5b0dc-40e9-83bc-94ee-b4e539edda2b
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q14860466 Skeletal System
is part of of	cartilage development skeletal system morphogenesis bone development
is part of of	wds:Q14877685-0210146F-4BCD-42F5-A84C-ECD81BF58380 wds:Q5104524-742FF90B-C4B3-44CE-8C93-C45603E685F1 wds:Q14877686-FEB6E97B-CEB9-46ED-BBBE-BFE742AF0516
is subclass of of	embryonic skeletal system development
is subclass of of	wds:Q14859970-8D8A77C2-4443-449D-B910-EECE45F452A7
is main subject of	A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome cDNA cloning and genomic structure of human bone morphogenetic protein-3B (BMP-3b) Fibroblast growth factor receptor 3 is a negative regulator of bone growth A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects Targeted disruption of Pax1 defines its null phenotype and proves haploinsufficiency Identification of a murine TEF-1-related gene expressed after mitogenic stimulation of quiescent fibroblasts and during myogenic differentiation Bcl-2 lies downstream of parathyroid hormone-related peptide in a signaling pathway that regulates chondrocyte maturation during skeletal development Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family The cartilage-derived, C-type lectin (CLECSF1): structure of the gene and chromosomal location Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene OP-1 cDNA encodes an osteogenic protein in the TGF-beta family Identification of transforming growth factor beta family members present in bone-inductive protein purified from bovine bone Recombinant Vgr-1/BMP-6-expressing tumors induce fibrosis and endochondral bone formation in vivo Osteogenic protein-2. A new member of the transforming growth factor-beta superfamily expressed early in embryogenesis Coding sequence and expression patterns of mouse chordin and mapping of the cognate mouse chrd and human CHRD genes Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome The mouse Engrailed-1 gene and ventral limb patterning Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse Regulation of anterior/posterior patterning of the axial skeleton by growth/differentiation factor 11 Characterization of a novel gene product (mammalian tolloid-like) with high sequence similarity to mammalian tolloid/bone morphogenetic protein-1 Bone morphogenetic protein: the molecularization of skeletal system development The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500) A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy SHOX mutations in dyschondrosteosis (Leri-Weill syndrome) Homology-mediated recombination between type I collagen gene exons results in an internal tandem duplication and lethal osteogenesis imperfecta Reduced bone density and osteoporosis associated with a polymorphic Sp1 binding site in the collagen type I alpha 1 gene Identification of novel pro-alpha2(IX) collagen gene mutations in two families with distinctive oligo-epiphyseal forms of multiple epiphyseal dysplasia. Down's syndrome-like skeletal abnormalities in Ets2 transgenic mice Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism A homozygous inactivating mutation in the parathyroid hormone/parathyroid hormone-related peptide receptor causing Blomstrand chondrodysplasia A novel mutation of the fibrillin gene causing ectopia lentis Activin increases bone mass and mechanical strength of lumbar vertebrae in aged ovariectomized rats

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