About: Synpolydactyly in mice with a targeted deficiency in the HoxD complex

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rdf:type	Item
description	artículu científicu espublizáu en 1996 (ast) vědecký článek publikovaný v roce 1996 (cs) 1996 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած (hyw) 1996 թվականի նոյեմբերին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована в листопаді 1996 (uk) article publié dans la revue scientifique Nature (fr) vedecký článok (publikovaný 1996/11/07) (sk) wetenschappelijk artikel (gepubliceerd op 1996/11/07) (nl) مقالة علمية (نشرت في 7-11-1996) (ar) scientific journal article (en) im November 1996 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28593833-5B199737-B530-47F8-8632-6D5D457A265D
publication date	1996-11-07 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28593833-FB947C21-B7CC-4117-8036-CAF3D4D5E76A
language of work or name	English
cites work	wds:Q28593833-354F43C4-E119-4ADA-A422-E5624229DEFD wds:Q28593833-47767DDA-3E2F-4A09-93FD-C0AEFC55FC78 wds:Q28593833-70336E6D-619A-4E9F-8BA7-56B1AADC78D3 wds:Q28593833-715A8E9F-E2A5-408A-AC5C-38E74596A423 wds:Q28593833-7549AA48-B053-4ECC-B8F8-2911B769B83F wds:Q28593833-7599F04F-77E2-4C08-A2F0-90776BBD1224 wds:Q28593833-81CF984F-146D-4D9C-BBC2-5CFC7D60C24E wds:Q28593833-83735D13-265B-4F28-88F9-91BC7119F2CA wds:Q28593833-9B8D553E-94B7-4EC9-BD36-863842DB29DA wds:Q28593833-DCA85C6B-93CF-43DD-882B-47AE0BB39EE5 wds:Q28593833-DF377CAC-C75A-4EFE-AF8E-310F75FCF278 wds:Q28593833-F0AD89C4-9948-430D-ADDA-EB3CA42AD391
cites work	Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13 Independent control of immunoglobulin switch recombination at individual switch regions evidenced through Cre-loxP-mediated gene targeting Recessive resistance to thyroid hormone in mice lacking thyroid hormone receptor beta: evidence for tissue-specific modulation of receptor function Colinearity and functional hierarchy among genes of the homeotic complexes Gene transpositions in the HoxD complex reveal a hierarchy of regulatory controls. Hox gene expression in teleost fins and the origin of vertebrate digits Disruption of the Hoxd-13 gene induces localized heterochrony leading to mice with neotenic limbs Axial skeleton homeosis and forelimb malformations in Hoxd-11 mutant mice Hox genes in vertebrate development Chromosome engineering in mice Localization of the syndactyly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?
author name string	wds:Q28593833-C3ADCA20-D3CF-4DA6-9261-0603724A4144
OpenCitations bibliographic resource ID	wds:Q28593833-DA5522CD-2431-45E5-889A-D3921A378DB3
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/3098521
author name string	J. Zákány
OpenCitations bibliographic resource ID	3098521
rdfs:label	Synpolydactyly in mice with a targeted deficiency in the HoxD complex (en) Synpolydactyly in mice with a targeted deficiency in the HoxD complex (nl) Synpolydactyly in mice with a targeted deficiency in the HoxD complex (ast)
skos:prefLabel	Synpolydactyly in mice with a targeted deficiency in the HoxD complex (en) Synpolydactyly in mice with a targeted deficiency in the HoxD complex (nl) Synpolydactyly in mice with a targeted deficiency in the HoxD complex (ast)
name	Synpolydactyly in mice with a targeted deficiency in the HoxD complex (en) Synpolydactyly in mice with a targeted deficiency in the HoxD complex (nl) Synpolydactyly in mice with a targeted deficiency in the HoxD complex (ast)
author	wds:Q28593833-B1461EF6-4390-4AA7-9959-50E9D55E7146
author	Denis Duboule
title	wds:Q28593833-A6073BD9-9C65-4848-BA71-402463D764F2
title	Synpolydactyly in mice with a targeted deficiency in the HoxD complex (en)
page(s)	wds:Q28593833-09559D1A-AC1A-48B4-9B94-6AB286E6A20A
page(s)	69–71
instance of	wds:Q28593833-A97CE310-F2C0-41D9-B631-084DA66F66D8
instance of	scholarly article
main subject	wds:Q28593833-02A8F610-2801-40F6-A614-759FBF625779 wds:Q28593833-7A663E13-24F1-484C-B098-705A0F75AD0E wds:Q28593833-86453114-A9C1-405B-BA29-8B675AC24180 wds:Q28593833-F81EE905-081A-41DC-9A48-5AC0839E7894
main subject	synpolydactyly Homeobox D12 Homeobox D11 Homeobox D13
PubMed ID	wds:Q28593833-F0981F6A-007A-4EA1-B80B-B9EE05EC08CA
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8900279
PubMed ID	8900279
published in	wds:Q28593833-8A6230D7-06A7-493B-88ED-ED8545EA7443
published in	Nature
issue	wds:Q28593833-D1A71AEC-09A4-444C-B1F8-A3EABC32A51C
volume	wds:Q28593833-86B6FF16-837C-4E61-A5A4-A1661F718C90
issue	6604
volume	384
DOI	wds:Q28593833-7C151B21-3D64-4BBC-B6F2-AE072199B369
DOI	http://dx.doi.org/10.1038/384069A0
DOI	10.1038/384069A0
Springer Nature article ID	wds:Q28593833-423CB8FD-E094-4642-9FF5-8D9753951A6B
Dimensions Publication ID	wds:Q28593833-A2477E3C-0258-4C05-81B0-296CE6CF9083
Springer Nature article ID	10.1038/384069a0
Dimensions Publication ID	1003514079
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28593833
is cites work of	Reduced proliferative capacity of hematopoietic stem cells deficient in Hoxb3 and Hoxb4. SALL1 truncated protein expression in Townes-Brocks syndrome leads to ectopic expression of downstream genes "Self-regulation," a new facet of Hox genes' function Posterior Hox gene expression in developing genitalia Vertebrate hox gene regulation: clustering and/or colinearity? Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome Polymorphism, shared functions and convergent evolution of genes with sequences coding for polyalanine domains Human HOX gene mutations Homeobox genes in embryogenesis and pathogenesis Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD cluster Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome Hoxd and Gli3 interactions modulate digit number in the amniote limb Evidence for regulation of cartilage differentiation by the homeobox gene Hoxc-8.

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