Prader-Willi and Angelman Syndrome - Wikidata - awgldk - TriplyDB

Prader-Willi and Angelman Syndrome

Prader-Willi and Angelman Syndrome

http://www.wikidata.org/entity/Q44013803

about

Prader-Willi and Angelman Syndrome

http://www.wikidata.org/entity/Q44013803

description

biological pathway in human

@en

name

Prader-Willi and Angelman Syndrome

@en

type

label

Prader-Willi and Angelman Syndrome

@en

prefLabel

Prader-Willi and Angelman Syndrome

@en

P1050

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Q44013803-2b7ede56-4ba0-5a86-697f-0b142f30be70

P1476

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P18

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P2410

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P2860

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Q44013803-4C3B4FB4-BCF9-4E0A-AE4B-15FCB3ECD496

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Q44013803-86AB2AEE-78B3-4805-96DF-BEA0B0EDB8F5

Q44013803-9A9EF661-40A8-4A3E-AA21-07F10B866F3F

Q44013803-9BB6D43B-F856-402F-A5C4-6EEA8D7AAD51

Q44013803-9DF2AFAD-1A70-4717-8B78-9F00FCF1A2F5

P2888

Q44013803-3B2BB6A2-33F0-4637-974E-ECA7A8A2D3C1

P31

Q44013803-CEA8AE85-1D0F-4428-804E-885E815E5F97

P373

Q44013803-bc0ec673-46c5-7ab8-e06d-bcdac69d28ff

P527

Q44013803-0AAA9958-2308-4017-B6AD-8646D69D6507

Q44013803-0B098160-0F00-4426-B252-AB66E5BF4313

Q44013803-0B6E22C3-A02A-41DE-9EEC-5D5734AA873E

Q44013803-14D26CCC-A519-45CD-899E-64563FB0C0EF

Q44013803-1615B6A7-4553-4CF0-9253-4EA96030ECA4

Q44013803-1A247911-9B2F-4C3E-9E64-45C519CC1513

Q44013803-21FF7E51-851D-4AA6-B4C8-593AF91A0607

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Q44013803-37559B7D-097F-496D-9270-EC9C5B842E05

Q44013803-3BA60E32-44E0-4D6B-AE22-CC6B28088DC1

P703

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P921

Q44013803-3322cfd3-4bc8-db20-4265-eaf62bf51ca6

P1050

Angelman syndrome

Prader–Willi syndrome

P1476

Prader-Willi and Angelman Syndrome

@en

P18

Prader-Willi%20and%20Angelman%20Syndrome%20%28Homo%20sapiens%29.svg

P2410

WP3998

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

P2860

Mammalian homologue of the Caenorhabditis elegans UNC-76 protein involved in axonal outgrowth is a protein kinase C zeta-interacting protein

A new pathway in the control of the initiation of puberty: the MKRN3 gene

Magel2 is required for leptin-mediated depolarization of POMC neurons in the hypothalamic arcuate nucleus in mice

Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior

Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth

Regulation of NKB pathways and their roles in the control of Kiss1 neurons in the arcuate nucleus of the male mouse.

Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development.

Increased alternate splicing of Htr2c in a mouse model for Prader-Willi syndrome leads disruption of 5HT2C receptor mediated appetite.

Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome.

Leptin signaling defects in a mouse model of Prader-Willi syndrome: An orphan genetic obesity syndrome no more?

P2888

P31

biological pathway

P373

Autosomal monosomies and deletions

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

P527

P703

P921

disease pathway