Invertebrate models of kallmann syndrome: molecular pathogenesis and new disease genes.

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Heparan Sulfate Proteoglycans Regulate Fgf Signaling and Cell Polarity during Collective Cell Migration.ZNF804A Transcriptional Networks in Differentiating Neurons Derived from Induced Pluripotent Stem Cells of Human Origin Feedback regulation of RTK signaling in development.

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Invertebrate models of kallmann syndrome: molecular pathogenesis and new disease genes.

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Invertebrate models of kallmann syndrome: molecular pathogenesis and new disease genes.

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Invertebrate models of kallmann syndrome: molecular pathogenesis and new disease genes.

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Invertebrate models of kallmann syndrome: molecular pathogenesis and new disease genes.

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P1476

Invertebrate models of kallmann syndrome: molecular pathogenesis and new disease genes

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Davide Andrenacci

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Elia Di Schiavi

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P2860

Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development

Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism

Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice

Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous system

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

Novel mechanisms of fibroblast growth factor receptor 1 regulation by extracellular matrix protein anosmin-1

Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome

Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family

The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome

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scholarly article

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10.2174/138920213804999174

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10.2174/1389202911314010002

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Elia Di Schiavi

Davide Andrenacci

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2013-03-01T00:00:00Z

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23997646

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pathogenesis

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Invertebrate models of kallmann syndrome: molecular pathogenesis and new disease genes.

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P2860

P2860

Invertebrate models of kallmann syndrome: molecular pathogenesis and new disease genes.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932