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rdf:type |
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lifeskim:mentions |
umls-concept:C0017337,
umls-concept:C0026809,
umls-concept:C0026882,
umls-concept:C0027794,
umls-concept:C0030705,
umls-concept:C0086418,
umls-concept:C0266453,
umls-concept:C0430054,
umls-concept:C1334043,
umls-concept:C1417388,
umls-concept:C1705053
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pubmed:issue |
5
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pubmed:dateCreated |
2001-4-26
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pubmed:abstractText |
Very little is known about the identity of genetic factors involved in the complex etiology of nonsyndromic neural tube defects (NTD). Potential susceptibility genes have emerged from the vast number of mutant mouse strains displaying NTD. Reasonable candidates are the human homologues of mice exencephaly genes Tfap2alpha and Msx2, which are expressed in the developing neural tube.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Codon,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Folate Receptors, GPI-Anchored,
http://linkedlifedata.com/resource/pubmed/chemical/Folic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Homeodomain Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/MSX2 protein,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cell Surface,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factor AP-2,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0040-3709
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pubmed:author |
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pubmed:copyrightInfo |
Copyright 2001 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:volume |
63
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
167-75
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:11320527-Alleles,
pubmed-meshheading:11320527-Anencephaly,
pubmed-meshheading:11320527-Animals,
pubmed-meshheading:11320527-Base Sequence,
pubmed-meshheading:11320527-Carrier Proteins,
pubmed-meshheading:11320527-Codon,
pubmed-meshheading:11320527-DNA, Complementary,
pubmed-meshheading:11320527-DNA-Binding Proteins,
pubmed-meshheading:11320527-Encephalocele,
pubmed-meshheading:11320527-Exons,
pubmed-meshheading:11320527-Folate Receptors, GPI-Anchored,
pubmed-meshheading:11320527-Folic Acid,
pubmed-meshheading:11320527-Gene Deletion,
pubmed-meshheading:11320527-Genotype,
pubmed-meshheading:11320527-Homeodomain Proteins,
pubmed-meshheading:11320527-Humans,
pubmed-meshheading:11320527-Mice,
pubmed-meshheading:11320527-Molecular Sequence Data,
pubmed-meshheading:11320527-Mutation,
pubmed-meshheading:11320527-Neural Tube Defects,
pubmed-meshheading:11320527-Pedigree,
pubmed-meshheading:11320527-Point Mutation,
pubmed-meshheading:11320527-Polymorphism, Genetic,
pubmed-meshheading:11320527-Polymorphism, Single-Stranded Conformational,
pubmed-meshheading:11320527-Receptors, Cell Surface,
pubmed-meshheading:11320527-Spinal Dysraphism,
pubmed-meshheading:11320527-Transcription Factor AP-2,
pubmed-meshheading:11320527-Transcription Factors
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pubmed:year |
2001
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pubmed:articleTitle |
A screen for mutations in human homologues of mice exencephaly genes Tfap2alpha and Msx2 in patients with neural tube defects.
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pubmed:affiliation |
Medizinisches Zentrum für Humangenetik, Philipps-Universität Marburg, 35033 Marburg, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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