Mutations in the netrin-1 gene cause congenital mirror movements.

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DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.

P2860

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Mutations in the netrin-1 gene cause congenital mirror movements.

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2017 nî lūn-bûn

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2017年学术文章

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name

Mutations in the netrin-1 gene cause congenital mirror movements.

@en

Mutations in the netrin-1 gene cause congenital mirror movements.

@nl

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Item

label

Mutations in the netrin-1 gene cause congenital mirror movements.

@en

Mutations in the netrin-1 gene cause congenital mirror movements.

@nl

prefLabel

Mutations in the netrin-1 gene cause congenital mirror movements.

@en

Mutations in the netrin-1 gene cause congenital mirror movements.

@nl

P1476

Mutations in the netrin-1 gene cause congenital mirror movements.

@en

P2093

Alexis Brice

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Christel Depienne

http://www.w3.org/2001/XMLSchema#string

Christine L Jasoni

http://www.w3.org/2001/XMLSchema#string

Coralie Fouquet

http://www.w3.org/2001/XMLSchema#string

Cécile Gallea

http://www.w3.org/2001/XMLSchema#string

Emmanuel Roze

http://www.w3.org/2001/XMLSchema#string

Florence Riant

http://www.w3.org/2001/XMLSchema#string

Isabelle Dusart

http://www.w3.org/2001/XMLSchema#string

Jean-Charles Lamy

http://www.w3.org/2001/XMLSchema#string

Jessica Andreani

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P2860

Disulfide bond assignments of secreted Frizzled-related protein-1 provide insights about Frizzled homology and netrin modules

Deleted in Colorectal Cancer (DCC) encodes a netrin receptor

NMR structure of the netrin-like domain (NTR) of human type I procollagen C-proteinase enhancer defines structural consensus of NTR domains and assesses potential proteinase inhibitory activity and ligand binding

Structures of netrin-1 bound to two receptors provide insight into its axon guidance mechanism

Structural Decoding of the Netrin-1/UNC5 Interaction and its Therapeutical Implications in Cancers

Netrins and DCC in the guidance of migrating neural crest-derived cells in the developing bowel and pancreas

Hierarchical organization of guidance receptors: silencing of netrin attraction by slit through a Robo/DCC receptor complex

High angular resolution diffusion imaging reveals intravoxel white matter fiber heterogeneity

Phenotype of mice lacking functional Deleted in colorectal cancer (Dcc) gene

Mapping netrin receptor binding reveals domains of Unc5 regulating its tyrosine phosphorylation

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3923-3936

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scholarly article

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10.1172/JCI95442

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English

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127

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2017-09-25T00:00:00Z

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28945198

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P921

Netrin 1

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5663368

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Mutations in the netrin-1 gene cause congenital mirror movements.

about

P2860

P2860

Mutations in the netrin-1 gene cause congenital mirror movements.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932