About: Polydactyly and ectopic ZPA formation in Alx-4 mutant mice

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scientific journal article

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rdf:type	Item
description	artículu científicu espublizáu en 1997 (ast) vědecký článek publikovaný v roce 1997 (cs) 1997 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած (hyw) 1997 թվականի հոտեմբերին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована в жовтні 1997 (uk) مقالة علمية (نشرت في أكتوبر 1997) (ar) vedecký článok (publikovaný 1997/10/01) (sk) article scientifique publié en 1997 (fr) wetenschappelijk artikel (gepubliceerd op 1997/10/01) (nl) scientific journal article (en) im Oktober 1997 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28585223-B84257AD-8756-4774-87F5-F5C95E5980E6
publication date	1997-10-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28585223-EDB56075-9784-474D-A26F-C3FF711E417A
language of work or name	English
author name string	wds:Q28585223-21CA9465-F47C-48CC-8628-04F613749379 wds:Q28585223-2A081C9F-BD84-4CD4-973D-F9126E0EFA26 wds:Q28585223-409153AE-A864-45BE-A194-3D28F584196F wds:Q28585223-431F7ED0-84BB-4D89-A425-B2E3EA0B4834 wds:Q28585223-5E3C28DD-DA4B-403F-9D81-05620D0E2740 wds:Q28585223-A435BF5F-85C8-43C2-A52A-0126357BF496 wds:Q28585223-DB5D1253-0572-4514-9C56-68A898C6FC3E
OpenCitations bibliographic resource ID	wds:Q28585223-7D29C035-5AE5-48C8-BE5F-2152D25CB6B0
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/455407
author name string	Magnuson MA Ji Q van der Meer R Niswender KD Qu S Keeney D Wisdom R
OpenCitations bibliographic resource ID	455407
rdfs:label	Polydactyly and ectopic ZPA formation in Alx-4 mutant mice (en) Polydactyly and ectopic ZPA formation in Alx-4 mutant mice (nl) Polydactyly and ectopic ZPA formation in Alx-4 mutant mice (ast)
skos:prefLabel	Polydactyly and ectopic ZPA formation in Alx-4 mutant mice (en) Polydactyly and ectopic ZPA formation in Alx-4 mutant mice (nl) Polydactyly and ectopic ZPA formation in Alx-4 mutant mice (ast)
name	Polydactyly and ectopic ZPA formation in Alx-4 mutant mice (en) Polydactyly and ectopic ZPA formation in Alx-4 mutant mice (nl) Polydactyly and ectopic ZPA formation in Alx-4 mutant mice (ast)
title	wds:Q28585223-91C34400-AFB2-4180-AAA2-8F94D6B8D056
title	Polydactyly and ectopic ZPA formation in Alx-4 mutant mice (en)
page(s)	wds:Q28585223-0B73C734-393A-4EE1-8ACA-B0885184648F
page(s)	3999-4008
instance of	wds:Q28585223-53A5C7D3-3D0C-419C-BB62-44841811E518
instance of	scholarly article
main subject	wds:Q28585223-85F22602-8C6A-4C6E-814A-B0CB653D7BFE wds:Q28585223-C3B05791-1B9D-4C7D-9DF3-09A9722751A9
main subject	polydactyly Aristaless-like homeobox 4
PubMed ID	wds:Q28585223-95843BFD-74A4-4753-9419-485C5575AB4E
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9374397
PubMed ID	9374397
published in	wds:Q28585223-1FE9AC32-F2F9-48B4-B428-1FF7CDBA70F6
published in	Development
issue	wds:Q28585223-EBA1CA8B-1F7D-4473-8A46-7743D14BE9C3
volume	wds:Q28585223-7143600A-1DC4-494F-959B-84590169A5E1
issue	20
volume	124
number of pages	wds:Q28585223-C65CB43F-A4AD-4540-B8A8-F3E61422980F
number of pages	10 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28585223
is cites work of	Transcriptional components of anteroposterior positional information during zebrafish fin regeneration Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities. The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500) Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype Alx4 and Msx2 play phenotypically similar and additive roles in skull vault differentiation. Phylogenetic conservation of a limb-specific, cis-acting regulator of Sonic hedgehog ( Shh) Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome Preaxial polydactyly caused by Gli3 haploinsufficiency is rescued by Zic3 loss of function in mice Cis-regulatory mutations in human disease GATA6 is a crucial regulator of Shh in the limb bud Preaxial polydactyly: interactions among ETV, TWIST1 and HAND2 control anterior-posterior patterning of the limb Oestrogen receptor-alpha regulates non-canonical Hedgehog-signalling in the mammary gland Role of homeobox genes in the patterning, specification, and differentiation of ectodermal appendages in mammals A genome-scale analysis of the cis-regulatory circuitry underlying sonic hedgehog-mediated patterning of the mammalian limb Mutual genetic antagonism involving GLI3 and dHAND prepatterns the vertebrate limb bud mesenchyme prior to SHH signaling Sonic hedgehog: restricted expression and limb dysmorphologies Fgf-dependent Etv4/5 activity is required for posterior restriction of Sonic Hedgehog and promoting outgrowth of the vertebrate limb Dorsoventral patterning of the mouse coat by Tbx15 Genetic analysis of Hedgehog signaling in ventral body wall development and the onset of omphalocele formation. FGF-regulated Etv genes are essential for repressing Shh expression in mouse limb buds The EDGE hypothesis: epigenetically directed genetic errors in repeat-containing proteins (RCPs) involved in evolution, neuroendocrine signaling, and cancer Twist1 activity thresholds define multiple functions in limb development Evolution of the Alx homeobox gene family: parallel retention and independent loss of the vertebrate Alx3 gene. A more efficient method to generate null mutants using Hprt-Cre with floxed alleles Limb anterior-posterior polarity integrates activator and repressor functions of GLI2 as well as GLI3 Novel exomphalos genetic mouse model: the importance of accurate phenotypic classification Homeobox genes in mammary gland development and neoplasia Impaired meningeal development in association with apical expansion of calvarial bone osteogenesis in the Foxc1 mutant. Neogenin regulates Sonic Hedgehog pathway activity during digit patterning Molecular anatomy of the developing limb in the coquí frog, Eleutherodactylus coqui HOXB13 and ALX4 induce SLUG expression for the promotion of EMT and cell invasion in ovarian cancer cells Impaired abdominal wall development and deficient wound healing in mice lacking aortic carboxypeptidase-like protein Alterations to the remote control of Shh gene expression cause congenital abnormalities Distinct populations within Isl1 lineages contribute to appendicular and facial skeletogenesis through the β-catenin pathway HoxB2, HoxB4 and Alx4 genes are downregulated in the cadmium-induced omphalocele in the chick model. Frontonasal Dysplasia: Towards an Understanding of Molecular and Developmental Aetiology.

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