About: Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse

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scientific journal article

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rdf:type	Item
description	artículu científicu espublizáu en 1998 (ast) vědecký článek publikovaný v roce 1998 (cs) 1998 թվականի սեպտեմբերին հրատարակված գիտական հոդված (hy) مقالة علمية (نشرت في سبتمبر 1998) (ar) 1998 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած (hyw) vedecký článok (publikovaný 1998/09/01) (sk) наукова стаття, опублікована у вересні 1998 (uk) wetenschappelijk artikel (gepubliceerd op 1998/09/01) (nl) im September 1998 veröffentlichter wissenschaftlicher Artikel (de) scientific journal article (en)
publication date	wds:Q28594147-77092027-4BBD-4547-9FDF-AD84298CC66D
publication date	1998-09-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28594147-118A7DAC-609E-44CF-98C3-40B34FB116EB
language of work or name	English
author name string	wds:Q28594147-12AA56B1-B916-48A4-A394-945F919CBD95 wds:Q28594147-13C26073-7CA6-4ED7-85F5-8D7CCACA66FA wds:Q28594147-D93E5615-4966-4916-8BEC-853FFDBAC6B9
author name string	L. C. Tsui M. A. Crackower J. Motoyama
rdfs:label	Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse (en) Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse (nl) Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse (ast)
skos:prefLabel	Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse (en) Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse (nl) Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse (ast)
name	Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse (en) Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse (nl) Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse (ast)
title	wds:Q28594147-0343BBF0-6AE9-42FA-AFEA-358C8E2F3E52
title	Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse (en)
page(s)	wds:Q28594147-8E8CA472-B347-405C-B179-C09FF6E644A4
page(s)	78–89
instance of	wds:Q28594147-EF09F74E-8968-4921-A211-067C5B10B913
instance of	scholarly article
main subject	wds:Q28594147-1E10FE1D-CC58-4B80-8D60-D04EAEF21CE5 wds:Q28594147-5767D69A-ECF2-4063-B83B-1CB0AF1E7750
main subject	Apical ectodermal ridge F-box and WD-40 domain protein 4
PubMed ID	wds:Q28594147-2FF48284-FD01-4D95-BEA6-A4277DB2FDD8
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9733575
PubMed ID	9733575
published in	wds:Q28594147-9EF48FDD-8C1C-4F06-83BA-DB351E24711B
published in	Developmental Biology
issue	wds:Q28594147-DBD00005-A205-47B8-BCB8-79FFE7B78994
volume	wds:Q28594147-70B6DE03-10B4-4B23-81E7-5219A48FFE87
issue	1
volume	201
DOI	wds:Q28594147-3FE847A6-45B4-42C7-953F-FC6C5170A7A4
DOI	http://dx.doi.org/10.1006/DBIO.1998.8938
DOI	10.1006/DBIO.1998.8938
ResearchGate publication ID	wds:Q28594147-57F4BB4C-7373-42DC-B447-AEB878B7D40E
ResearchGate publication ID	13551384
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28594147
is cites work of	Split hand foot malformation is associated with a reduced level of Dactylin gene expression The Dlx5 and Dlx6 homeobox genes are essential for craniofacial, axial, and appendicular skeletal development Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27. A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant A symphony of regulations centered on p63 to control development of ectoderm-derived structures Clinical, genetic, and molecular aspects of split-hand/foot malformation: an update. Genetically regulated epigenetic transcriptional activation of retrotransposon insertion confers mouse dactylaplasia phenotype Identification of evolutionarily conserved regulatory elements in the mouse Fgf8 locus Vertebrate limb development and possible clues to diversity in limb form. Split-hand/foot malformation - molecular cause and implications in genetic counseling. Asymmetric limb malformations in a new transgene insertional mutant, footless. Disrupting the establishment of polarizing activity by teratogen exposure. DLX5, FGF8 and the Pin1 isomerase control ΔNp63α protein stability during limb development: a regulatory loop at the basis of the SHFM and EEC congenital malformations A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation. Central and ulnar cleft hands: a review of concurrent deformities in a series of 47 patients and their pathogenesis Distal limb malformations: underlying mechanisms and clinical associations A novel intergenic ETnII-β insertion mutation causes multiple malformations in polypodia mice Are there CAG repeat expansion-related disorders outside the central nervous system? Spalthand-/Spaltfußfehlbildungen
is cites work of	wds:Q34230565-3D76BCE2-1C45-476B-BE09-3B2839EF6F66 wds:Q52104707-73024D29-2EBE-4312-B904-C0D297FDF5D4 wds:Q58379789-2BD9E751-9297-4E02-80E2-6D68D8A157F4 wds:Q35067250-449028A3-8248-47AC-B3C0-BCD1DCB1FDD1 wds:Q34446570-820F8CAC-6A02-4078-91B0-5E57E7877B67 wds:Q52579802-A6825918-A60B-40AB-A534-A5465E1A536C wds:Q34397705-48275914-C01F-40EF-A485-A78061477463 wds:Q37540407-54B557E5-770A-45D7-B0D0-98082DFD02CB wds:Q52122046-5EE71B60-9296-49EB-B14B-89C5F443EE5D wds:Q52173589-48914D51-BE60-413C-8DE6-F61EB38D8301 wds:Q39020902-3B492FE9-58F2-4C18-A48B-44FC677F945B wds:Q57234129-61224B34-E6FB-4F15-8216-5742D4BB8029 wds:Q54782646-DBAD1CE4-6239-4B7D-8491-4E80EB23647D wds:Q38119136-C8E3DC33-D70E-41D3-870A-4E3448AD8282 wds:Q24675473-EAC899C2-5944-4166-A4FC-2DB209045EBF wds:Q34141916-23B64C2D-A037-454C-91DF-1974DC26A2E3 wds:Q28512070-A16F3E59-9334-4E91-B5AE-3586BA946955 wds:Q36277190-52DB960F-A5F0-4E1F-ABAE-6D692CD02CF6 wds:Q37895920-C08B0D61-55E2-4F13-9FFD-5BA8C4C1B7DF
is pr:P248 of	wdref:547329d076103a3824fc66548c91d2abcb1bd2a2

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