About: Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4

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About: Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4 Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	artículu científicu espublizáu en 1997 (ast) vědecký článek publikovaný v roce 1997 (cs) 1997 թվականի օգոստոսին հրատարակված գիտական հոդված (hy) 1997 թուականի Օգոստոսին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована в серпні 1997 (uk) vedecký článok (publikovaný 1997/08/15) (sk) مقالة علمية (نشرت في 15-8-1997) (ar) wetenschappelijk artikel (gepubliceerd op 1997/08/15) (nl) scientific journal article (en) im August 1997 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28587988-B5493684-0A72-4957-9FA8-8898B7190B07
publication date	1997-08-15 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28587988-42AABA42-6268-4C71-ABE5-D625C5972B0B
language of work or name	English
cites work	wds:Q28587988-EFBFB05B-D66C-4C0C-AC24-B9BA8D01C9F2
cites work	Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice
author name string	wds:Q28587988-1C8CFD83-0E8A-4702-B0F8-3CCA5927D05C wds:Q28587988-27ECF6AA-30DB-4568-9DB2-88D051738419 wds:Q28587988-512A9D96-CAFF-4EB4-8A8B-215EA9C243A1 wds:Q28587988-752618E2-C955-42B8-8C60-17C4E198D497 wds:Q28587988-78276AEE-EED3-4575-B091-CC533A449485 wds:Q28587988-B6AB69B4-918A-4565-AE3D-50C59BE9674C
author name string	B. L. Hogan G. E. Winnier A. B. Fogo J. J. Schrick L. K. Hargett N. R. Dunn
rdfs:label	Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4 (en) Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4 (nl) Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4 (ast)
skos:prefLabel	Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4 (en) Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4 (nl) Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4 (ast)
name	Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4 (en) Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4 (nl) Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4 (ast)
title	wds:Q28587988-260ED03D-2ED5-48B3-A675-DFB9BAEAFB04
title	Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4 (en)
page(s)	wds:Q28587988-FA02F8EE-ECAF-4E97-ABC8-53651A972E68
page(s)	235–247
instance of	wds:Q28587988-8EFBDE90-0417-40C7-87AA-B14D1E37EFE1
instance of	scholarly article
main subject	wds:Q28587988-032B16EA-4F14-412B-A8A2-EB018E536A69 wds:Q28587988-8478F54C-0D21-4D5F-BD5B-9084C2DB5EEC wds:Q28587988-8828C484-BC48-4B9E-8B68-69F7065B5CD9 wds:Q28587988-9BF9066F-3BBC-4B93-83C3-578122BFDA3C wds:Q28587988-9F6AA54C-B471-4910-9C37-CDE8171376A4 wds:Q28587988-D0DE3B2F-379D-4B1E-BC28-761DF6392594
main subject	phenotype haploinsufficiency Bone morphogenetic protein 4 Aristaless-like homeobox 4 heterozygosity GLI-Kruppel family member GLI3
PubMed ID	wds:Q28587988-29F02357-BBA8-4F54-A14F-4B1619046987
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9268572
PubMed ID	9268572
published in	wds:Q28587988-4170C159-51BE-4EE1-9D36-9956B217B498
published in	Developmental Biology
issue	wds:Q28587988-4A959030-63C4-46D7-B46B-26C6064365F9
volume	wds:Q28587988-80B54617-9ED2-414A-BB16-275F893F1129
issue	2
volume	188
DOI	wds:Q28587988-3FE5115A-D045-42C1-A717-099F5469ACA8
DOI	http://dx.doi.org/10.1006/DBIO.1997.8664
DOI	10.1006/DBIO.1997.8664
ResearchGate publication ID	wds:Q28587988-0E6EC66F-9B51-403E-9CAF-80369A2C28EB
ResearchGate publication ID	13950890
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28587988
is cites work of	Bmp in podocytes is essential for normal glomerular capillary formation Skeletal abnormalities in doubly heterozygous Bmp4 and Bmp7 mice Smad expression during kidney development Bmp2 and Bmp4 exert opposing effects in hypoxic pulmonary hypertension Ski is involved in transcriptional regulation by the repressor and full-length forms of Gli3 Specification of dorsal spinal cord interneurons Foxg1 promotes olfactory neurogenesis by antagonizing Gdf11. Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways Loss of the serine/threonine kinase fused results in postnatal growth defects and lethality due to progressive hydrocephalus The bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization Bone morphogenetic protein receptor complexes on the surface of live cells: a new oligomerization mode for serine/threonine kinase receptors Eye and neural defects associated with loss of GDF6 Evidence for an early role for BMP4 signaling in thymus and parathyroid morphogenesis IL-7Ralpha and E47: independent pathways required for development of multipotent lymphoid progenitors Eya 1 acts as a critical regulator for specifying the metanephric mesenchyme Defects in limb, craniofacial, and thymic development in Jagged2 mutant mice Smad1 and Smad8 function similarly in mammalian central nervous system development. Tissue-specific requirements of beta-catenin in external genitalia development JNK initiates a cytokine cascade that causes Pax2 expression and closure of the optic fissure Levels of Gli3 repressor correlate with Bmp4 expression and apoptosis during limb development. Developmental expression and function of Bmp4 in spermatogenesis and in maintaining epididymal integrity. Bmp4 is required for the generation of primordial germ cells in the mouse embryo Bone morphogenetic protein signaling regulates gastric epithelial cell development and proliferation in mice Msx genes are important apoptosis effectors downstream of the Shh/Gli3 pathway in the limb Syndactyly and preaxial synpolydactyly in the single Sfrp2 deleted mutant mice Msx1 and Msx2 in limb mesenchyme modulate digit number and identity Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure Renal development: perspectives on a Wnt-dependent process Delineating a conserved genetic cassette promoting outgrowth of body appendages

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