About: GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

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scientific article published in Nature

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rdf:type	Item
description	artículu científicu (ast) wetenschappelijk artikel (nl) article publié dans la revue scientifique Nature (fr) im August 1991 veröffentlichter wissenschaftlicher Artikel (de) নেচারে প্রকাশিত বৈজ্ঞানিক প্রবন্ধ (bn) scientific article published in Nature (en) наукова стаття, опублікована в Nature в серпні 1991 (uk)
publication date	wds:Q55670532-60E696A3-9129-4AEA-B5AE-34979E95615B
publication date	1991-08-08 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q55670532-4FA9D064-0B89-48A6-86DB-15DFB4DBD7A6
language of work or name	English
exact match	wds:Q55670532-D732E5E3-CAE3-4EE8-8168-0CF860696F34
exact match	https://scigraph.springernature.com/pub.10.1038/352539a0
cites work	wds:Q55670532-17C91789-7862-4D2B-B72A-CFA1240B1861 wds:Q55670532-18A0D000-A082-4BCF-8B29-BC9C3AB76E7B wds:Q55670532-2BC04C72-67DE-4C81-BEBD-8F09D41D4044 wds:Q55670532-3DE4A5A7-6F3D-427E-AE7E-4EE04776C508 wds:Q55670532-4511766F-3BA9-4B34-9533-D16903DCEF25 wds:Q55670532-4CA99B61-6A2D-433D-9914-6B11AC2215C2 wds:Q55670532-72F60F21-5371-4C45-9D33-96C706561E95 wds:Q55670532-7F3A921F-5A7C-4FF3-B014-828583227358 wds:Q55670532-88DC8A4E-166D-41E1-A2FF-AB45F86C2970 wds:Q55670532-9BFDF871-8BD8-4218-994E-856858671D2A wds:Q55670532-E8210B02-B6E3-4D3A-B03C-9C007409B1FA wds:Q55670532-F357A96C-F859-4684-8325-05DF1169A01A wds:Q55670532-F7205619-1889-4FDE-BBAA-26B8DDB553CA
cites work	Regional assignment of 41 human DNA fragments on chromosome 7 by means of a somatic cell hybrid panel GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity Genomic sequencing Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13. A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly-craniofacial anomalies syndrome The GLI-Kruppel family of human genes The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13). Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13). Greig cephalopolysyndactyly syndrome: a possible mouse homologue (Xt-extra toes) Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes Retinoids and vertebrate limb pattern formation
author name string	wds:Q55670532-B73DE257-1359-4E81-AFF9-D5A2C1138798 wds:Q55670532-BF6931B5-133C-4975-953C-3A091B2EC504
author name string	K H Grzeschik A Vortkamp
rdfs:label	GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families (en) GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families (nl)
skos:prefLabel	GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families (en) GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families (nl)
name	GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families (en) GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families (nl)
author	wds:Q55670532-DCE726EA-B17D-4A5C-B3BF-A70D832FB176
author	Manfred Gessler
title	wds:Q55670532-49C87C5A-CF21-4658-8364-D661D893C092
title	GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families (en)
page(s)	wds:Q55670532-14E40765-87CB-4FE6-A6CD-59092A918B2E
page(s)	539-40
instance of	wds:Q55670532-FB3758FC-13B1-4BE8-83A1-857971F075B6
instance of	scholarly article
PubMed ID	wds:Q55670532-2912AAC2-F2D3-474E-84C3-859221D456BF
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1650914
PubMed ID	1650914
published in	wds:Q55670532-C8C8B25C-3FAC-4E6D-B225-21EBDDFAE099
published in	Nature
issue	wds:Q55670532-43224125-24EC-43B3-92FE-A863737B054B
volume	wds:Q55670532-B001A023-1B37-47EB-8762-5F6187AE2079
issue	6335
volume	352
DOI	wds:Q55670532-68922A41-73CC-4C15-9CA3-E022149B31EE
DOI	http://dx.doi.org/10.1038/352539A0
DOI	10.1038/352539A0
ResearchGate publication ID	wds:Q55670532-1D9D8B63-6E9B-4C72-A001-473F9C5EABDD
ResearchGate publication ID	21504650
Dimensions Publication ID	wds:Q55670532-2496C2AA-52B4-454F-80AA-A2A20268842E
Dimensions Publication ID	1040461468
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55670532
is cites work of	The sonic hedgehog-patched-gli pathway in human development and disease Twist and shout Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22 Opitz G/BBB syndrome: clinical comparisons of families linked to Xp22 and 22q, and a review of the literature Duplicated KOX zinc finger gene clusters flank the centromere of human chromosome 10: evidence for a pericentric inversion during primate evolution Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family Perspectives on zinc finger protein function and evolution--an update Conjunction dysfunction: CBP/p300 in human disease. The molecular pathology of syndromic craniosynostosis Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome A single-gene explanation for the probability of having idiopathic talipes equinovarus Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalities. Context-dependent signal integration by the GLI code: the oncogenic load, pathways, modifiers and implications for cancer therapy Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly. The molecular basis of genetic dominance The VACTERL association: lessons from the Sonic hedgehog pathway gli, a zinc finger transcription factor and oncogene, is expressed during normal mouse development Genetically altered mouse models: the good, the bad, and the ugly GLI activates transcription through a herpes simplex viral protein 16-like activation domain. Developmental roles and clinical significance of hedgehog signaling Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene Human haploinsufficiency — one for sorrow, two for joy Phosphorylation of Gli2 by protein kinase A is required for Gli2 processing and degradation and the Sonic Hedgehog-regulated mouse development Holoprosencephaly: a paradigm for the complex genetics of brain development.

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