FGFR1 and anosmin-1 underlying genetically distinct forms of Kallmann syndrome are co-expressed and interact in olfactory bulbs

Development Genes and Evolution

Volumn 217, Issue 2, 2007, Pages 169-175

  Ayari, Besma ^a,b   Soussi Yanicostas, Nadia ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b SORBONNE UNIVERSITÉ   (France)

Author keywords

Anosmin 1; FGF signalling; FGFR1; Kallmann syndrome; Olfactory bulbs

Indexed keywords

ANOSMIN 1; FIBROBLAST GROWTH FACTOR RECEPTOR 1; SCLEROPROTEIN; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; EMBRYO; EMBRYO DEVELOPMENT; EMBRYO PATTERN FORMATION; EVOLUTIONARY DEVELOPMENTAL BIOLOGY; GENE INTERACTION; IMMUNOPRECIPITATION; KALLMANN SYNDROME; NONHUMAN; OLFACTORY BULB; OLFACTORY SYSTEM; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; RAT; SIGNAL TRANSDUCTION;

ANIMALS; CHO CELLS; CRICETINAE; CRICETULUS; EXTRACELLULAR MATRIX PROTEINS; FEMALE; GENE EXPRESSION; HUMANS; IMMUNOHISTOCHEMISTRY; KALLMANN SYNDROME; MODELS, BIOLOGICAL; NERVE TISSUE PROTEINS; OLFACTORY BULB; PREGNANCY; RATS; RATS, WISTAR; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 1; TRANSFECTION;

RATTUS;

EID: 33846850357     PISSN: 0949944X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00427-006-0125-0     Document Type: Article

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