About: The mouse mutant Polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene Gli3

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About: The mouse mutant Polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene Gli3 Goto Sponge NotDistinct Permalink

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scientific article published on 01 June 1994

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 1994 (uk) article scientifique publié en 1994 (fr) artículu científicu espublizáu en xunu de 1994 (ast) scientific article published on 01 June 1994 (en)
publication date	wds:Q72090638-F6CC2C3F-083E-45A7-AFE2-D7BC8B09C6D4
publication date	1994-06-01 00:00:00Z (xsd:dateTime)
exact match	wds:Q72090638-75F156CD-6028-4AD4-86E4-50DE753EE33B
exact match	https://scigraph.springernature.com/pub.10.1007/bf00356560
cites work	wds:Q72090638-0045ECFB-6467-4FC8-84DF-EF87C7822ADA wds:Q72090638-013AE8DF-14E7-4163-885A-860BF096AC6A wds:Q72090638-0C9743B2-B439-417B-8654-C1B1F5F48270 wds:Q72090638-1889394F-7863-4023-9870-620FB07711F6 wds:Q72090638-1E3C3E40-E1BA-4027-B977-26975BC18C71 wds:Q72090638-1FFF8D18-6809-4B26-9D60-FA925CD58889 wds:Q72090638-250AC1D3-BEBD-4DDC-A60B-9BBFBF1195CD wds:Q72090638-3B30C2C0-BC96-433E-A449-D42D6A56D90C wds:Q72090638-417AC2FA-EC8C-4ED7-8991-CABCBA48492B wds:Q72090638-417CE957-8FFA-438E-8A37-08A280ACF0B4 wds:Q72090638-43807302-C9C1-4444-AB4D-E4928F5F29D0 wds:Q72090638-59CBFD51-9E3F-4997-9A38-383B5521354E wds:Q72090638-86CF31BF-E2E9-432A-B4DE-9AFB06D2FDF5 wds:Q72090638-9BBBF840-040E-482A-A13A-5CC3EFABD3C3 wds:Q72090638-B8F210D8-07DD-41A2-9DFD-428E9E5E5BD2 wds:Q72090638-DCE844E5-0BF3-4018-A908-5C34A59772DA wds:Q72090638-DFA9C89C-15E8-41EC-9EE2-36FA540A5C27 wds:Q72090638-E654A961-BA0D-497C-8FDF-6BD807675A0E wds:Q72090638-EEFCAF78-5E8D-4610-8A51-5E5339853EEC wds:Q72090638-F1064379-EC5B-41CB-8E4F-DB09146F901B wds:Q72090638-FA9FDC15-F4BA-49AE-9061-120C04E4EA99 wds:Q72090638-FD73EFA1-9761-473D-9DF7-1BAA867510E0
cites work	Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene Molecular analysis of the C. elegans sex-determining gene tra-1: a gene encoding two zinc finger proteins Zinc finger point mutations within the WT1 gene in Wilms tumor patients Pax in development GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity A mouse model of greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt) splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3 The molecular basis of the undulated/Pax-1 mutation Mouse small eye results from mutations in a paired-like homeobox-containing gene Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I) An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome Greig cephalopolysyndactyly syndrome: a possible mouse homologue (Xt-extra toes) Polydactyly Nagoya, Pdn: A new mutant gene in the mouse Occurrences and linkage relations of the mutant ‘extra-toes’ in the mouse Developmental brain abnormalities accompanied with the retarded production of S-100 beta protein in genetic polydactyly mice. Extra-toes: anew mutant gene causing multiple abnormalities in the mouse. Expression of the zinc finger gene Gli3 is affected in the morphogenetic mouse mutant extra-toes (Xt) Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra-toes (Xt) Molecular linkage of the morphogenetic mutation add and the zinc finger gene Gli3 Localization of genes and anonymous DNA probes on the short arm of Chromosome 7
author name string	wds:Q72090638-2BEFB790-6860-41C2-BD1C-879AF6F1830D wds:Q72090638-41F40B37-BC31-42B2-89EA-6E8C6B88F763
author name string	U Rüther S I Oda
rdfs:label	The mouse mutant Polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene Gli3 (en) The mouse mutant Polydactyly Nagoya (nl)
skos:prefLabel	The mouse mutant Polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene Gli3 (en) The mouse mutant Polydactyly Nagoya (nl)
name	The mouse mutant Polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene Gli3 (en) The mouse mutant Polydactyly Nagoya (nl)
author	wds:Q72090638-5F8500B7-7969-44FC-87A0-F3DCCA66C2E2
author	Thomas Schimmang
title	wds:Q72090638-0EC02067-072B-4841-B2AD-A528BBB9FCCF
title	The mouse mutant Polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene Gli3 (en)
page(s)	wds:Q72090638-D8A95AA4-3715-48C2-88A4-B5D976D23F04
page(s)	384-386
instance of	wds:Q72090638-87E7690A-05F3-49C3-8B9C-9B6129932909
instance of	scholarly article
main subject	wds:Q72090638-34A27AB2-0801-440D-B8A7-5DB7CB960138
main subject	polydactyly
PubMed ID	wds:Q72090638-53BF5811-F317-4A2A-B423-22A08E7011DD
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8043956
PubMed ID	8043956
published in	wds:Q72090638-2B85936B-8D29-4715-8F5A-D0BF03C73B8E
published in	Mammalian Genome
issue	wds:Q72090638-9FADA226-264D-42AB-ADD2-BCDDE5BEE970
volume	wds:Q72090638-3A18A9B3-82F8-42C0-8347-FD1BF0E3A4CB
issue	6
volume	5
number of pages	wds:Q72090638-2C1DB314-04FD-42F4-ADCC-19EEAFA13236
number of pages	3 (xsd:decimal)
DOI	wds:Q72090638-A5DA9199-345D-496B-8258-929F2970E23D
DOI	http://dx.doi.org/10.1007/BF00356560
DOI	10.1007/BF00356560
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q72090638
is cites work of	The hedgehog signaling network Lamination of the cerebral cortex is disturbed in Gli3 mutant mice. Mutation in GLI3 in postaxial polydactyly type A Evidence for genetic control of Sonic hedgehog by Gli3 in mouse limb development The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations Human GLI3 intragenic conserved non-coding sequences are tissue-specific enhancers Human intronic enhancers control distinct sub-domains of Gli3 expression during mouse CNS and limb development Normal development of serotonergic neurons in mice lacking S100B. Life-and-death decisions influenced by retinoids Identification and functional characterization of novel transcriptional enhancers involved in regulating human GLI3 expression during early development. High-resolution mapping of the Gli3 deletion in the mouse extra-toesH mutant.

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