A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome. - Wikidata - wikimedia - TriplyDB

A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome.

A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome.

http://www.wikidata.org/entity/Q37746507

about

Loss of HAI-2 in mice with decreased prostasin activity leads to an early-onset intestinal failure resembling congenital tufting enteropathy.

P2860

Q54948226-4093B908-96AC-455C-A821-AA7132C0C260

P2860

A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome.

http://www.wikidata.org/entity/Q37746507

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 24 February 2017

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome.

@en

A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome.

@nl

type

label

A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome.

@en

A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome.

@nl

prefLabel

A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome.

@en

A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome.

@nl

P1433

Q37746507-82188C39-CFF0-4616-A1F3-54BED94EE648

P1476

Q37746507-16165598-EC80-4CD7-88E0-E11811E2B5C2

P2093

Q37746507-0AAF98E3-C4A4-4772-B1ED-A89B335C436E

Q37746507-236601FE-94A1-4801-A0C2-B3C8DBB6329E

Q37746507-37B1BE93-2B5B-48E9-9D8C-0AD6740A78E5

Q37746507-3AC75296-99C0-4083-87E7-A53A4F247094

Q37746507-556F47ED-423A-4FC8-8700-554C84C2682B

Q37746507-7BFBD749-406D-4C79-8F82-9859774DED34

Q37746507-8CB04B97-C522-4522-B97A-43AF84B9E60B

Q37746507-C5D17367-F5C9-4E13-9F30-3DA30A2EED6D

Q37746507-C97B87C4-4EAB-462E-AAB1-08AB534CB81C

Q37746507-EA3045D9-7C0C-48AA-8842-5F3F734C046A

P2860

Q37746507-02195462-E530-42CB-B00A-F4BDEF6B6F5F

Q37746507-054365B2-6C88-470C-A14D-49B3DDA6BB1E

Q37746507-2211459E-F8EE-429F-AD36-F3EFFE8EFE22

Q37746507-31336DF9-8E5F-4A77-AE96-940CD2E0ECC1

Q37746507-741ED6FE-1607-4046-BAB4-5F248AA96A2B

Q37746507-7A40480E-1070-4789-85D9-AE066DF8332B

Q37746507-7AADE09F-47D7-422C-BCE2-B7E80B04644C

Q37746507-7CA3C4A8-BE38-4476-B9F5-29178EE2324E

Q37746507-AD6CCC46-F363-4912-B5C3-63D983A7486D

Q37746507-AFDAEE74-1CB9-4B51-A484-FBC210107113

P304

Q37746507-57578553-4698-4630-8E52-FA2D8DEB6165

P31

Q37746507-A7A426C5-B66F-461E-B85E-6808D77070AE

P356

Q37746507-3A03DD78-A586-4B95-8C9C-EB5C5C510FE4

P433

Q37746507-14AAEADB-68F5-4CDB-858E-948C5623B2C9

P478

Q37746507-096D2797-9F9D-4E21-A06D-CD3456B89CDE

P50

Q37746507-19FD70A5-AAED-41B6-B3FA-1F3949AA419C

Q37746507-6FDA6FB9-AC4A-4972-83B5-FC7C0850DA1C

Q37746507-E7DEA8DA-8347-4F4D-8294-9408F2924691

Q37746507-F41B3135-8E11-4672-A2D4-1D6F1B628E4F

P577

Q37746507-E6134094-E7FA-42DA-A56F-062DFD7D40F5

P698

Q37746507-7A820518-D6B0-40B6-82FC-CB3A8010F153

P921

Q37746507-CC2D92FE-354A-4A5B-AD43-AD7A8D16868E

P932

Q37746507-CB1597BA-AE5A-40FA-95C6-1D31E213D0A0

P356

P1433

P1476

A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome

@en

P2093

Iris Bachmann

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

M Cecilia Penedo

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

Markus Neuditschko

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

Martina Vitková

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

Monika M Welle

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

Nadja Tarasova

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

Nicolò Sirtori

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

Stefan Rieder

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

Theresa Hiemesch

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

Vidhya Jagannathan

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

P2860

New member of the winged-helix protein family disrupted in mouse and rat nude mutations

Ichthyosis, follicular atrophoderma, and hypotrichosis caused by mutations in ST14 is associated with impaired profilaggrin processing

Coat variation in the domestic dog is governed by variants in three genes

PLINK: a tool set for whole-genome association and population-based linkage analyses

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

Assignment1 of human putative tumor suppressor genes ST13 (alias SNC6) and ST14 (alias SNC19) to human chromosome bands 22q13 and 11q24-->q25 by in situ hybridization

A mutation in hairless dogs implicates FOXI3 in ectodermal development.

A deletion in FOXN1 is associated with a syndrome characterized by congenital hypotrichosis and short life expectancy in Birman cats.

Autosomal recessive ichthyosis with hypotrichosis caused by a mutation in ST14, encoding type II transmembrane serine protease matriptase.

Loss of proteolytically processed filaggrin caused by epidermal deletion of Matriptase/MT-SP1.

P304

1315-1321

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

P31

scholarly article

P356

10.1534/G3.117.039511

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

P433

4

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

P478

7

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

P50

Paola Roccabianca

P577

2017-04-03T00:00:00Z

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

P698

28235824

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

P921

P932

5386879

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