Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1

Nature Genetics

Volumn 44, Issue 6, 2012, Pages 709-713

  Bonnard, Carine ^a   Strobl, Anna C ^b   Shboul, Mohammad ^a   Lee, Hane ^c   Merriman, Barry ^c   Nelson, Stanley F ^c   Ababneh, Osama H ^d   Uz, Elif ^e,f   Güran, Tülay ^g   Kayserili, Hülya ^h   Hamamy, Hanan ^i,j   Reversade, Bruno ^a,k  

^a INSTITUTE OF MEDICAL BIOLOGY   (Singapore)

^b NATIONAL INSTITUTE FOR MEDICAL RESEARCH   (United Kingdom)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d UNIVERSITY OF JORDAN   (Jordan)

^e DUZCE UNIVERSITY   (Turkey)

^f HACETTEPE UNIVERSITY   (Turkey)

^g MARMARA UNIVERSITY SCHOOL OF MEDICINE   (Turkey)

^h ISTANBUL UNIVERSITY   (Turkey)

ⁱ GENEVA UNIVERSITY HOSPITALS   (Switzerland)

^j National Center for Diabetes Endocrinology and Genetics Jordan   (Jordan)

^k NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA ACTIN; BETA CATENIN; HOMEODOMAIN INTERACTING PROTEIN KINASE 2; LACTACYSTIN; PROTEIN TRPS1; STROMAL CELL DERIVED FACTOR 1; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR GATA 3; TRANSCRIPTION FACTOR IRX5; UNCLASSIFIED DRUG; ZINC FINGER PROTEIN;

ARTICLE; BONE MALFORMATION; BRAIN MALFORMATION; CELL MIGRATION; CELL POPULATION; CONGENITAL HEART MALFORMATION; CONTROLLED STUDY; CRANIOFACIAL DEVELOPMENT; CRANIOFACIAL MALFORMATION; EMBRYO; EMBRYO DEVELOPMENT; FACE MALFORMATION; GENE; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; GENETIC TRANSCRIPTION; GENITAL MALFORMATION; GERM CELL; HOMEOSTASIS; HOMOZYGOSITY; HUMAN; IN VIVO STUDY; IRX5 GENE; NONHUMAN; NUCLEOTIDE SEQUENCE; ONTOGENY; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; SDF1 GENE; SIGNAL TRANSDUCTION; STEM CELL; XENOPUS LAEVIS;

ABNORMALITIES, MULTIPLE; ANIMALS; BASE SEQUENCE; BONE AND BONES; BRAIN; BRANCHIAL REGION; CRANIOFACIAL ABNORMALITIES; DNA-BINDING PROTEINS; FEMALE; GATA3 TRANSCRIPTION FACTOR; GENE EXPRESSION REGULATION; GONADS; HEART DEFECTS, CONGENITAL; HOMEODOMAIN PROTEINS; HUMANS; MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; SYNDROME; TRANSCRIPTION FACTORS; XENOPUS LAEVIS; XENOPUS PROTEINS;

XENOPUS LAEVIS;

EID: 84861582022     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.2259     Document Type: Article

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