ALDH1A2 (RALDH2) genetic variation in human congenital heart disease. - Wikidata - awgldk - TriplyDB

ALDH1A2 (RALDH2) genetic variation in human congenital heart disease.

ALDH1A2 (RALDH2) genetic variation in human congenital heart disease.

http://www.wikidata.org/entity/Q30877299

about

Increased dietary intake of vitamin A promotes aortic valve calcification in vivo The neural crest in cardiac congenital anomalies Myocardial alternative RNA splicing and gene expression profiling in early stage hypoplastic left heart syndrome Aldehyde dehydrogenases: from eye crystallins to metabolic disease and cancer stem cells VISIONET: intuitive visualisation of overlapping transcription factor networks, with applications in cardiogenic gene discovery.Tetralogy of Fallot and Hypoplastic Left Heart Syndrome - Complex Clinical Phenotypes Meet Complex Genetic Networks Congenital diaphragmatic hernia with concurrent aplasia of the pericardium in a foal Partitioning the heart: mechanisms of cardiac septation and valve development Duplication of the ALDH1A2 gene in association with pentalogy of Cantrell: a case report.Retinaldehyde dehydrogenase enzymes regulate colon enteric nervous system structure and function.

P2860

Q24630155-0C83F267-F9D8-45DC-BA8B-AF5174A7E93C Q27024385-7B396BD9-F7C0-4D6C-9EC8-D6020ACDCCDB Q28732385-942F8BAE-5366-41FB-80D2-4C73F3114C0D Q34026132-71565010-6608-440B-A19B-B86DAAFC16F4 Q35589296-E669D21B-2C34-46DE-B9AD-0EB393597BA2 Q35697680-03F0D6BE-A9E7-44A4-AF74-64BC74AB6874 Q35881357-7798C59F-497F-47D4-8CD7-31F8ACAC2E99 Q36178682-BDAEB58B-7BE0-489D-8BFC-37E523BD96DD Q41930983-445098F3-512A-4E16-9C8A-F7E0B1F8E315 Q42077729-6146DB15-EAF2-4580-9DED-3C7758F8C3E3

P2860

ALDH1A2 (RALDH2) genetic variation in human congenital heart disease.

http://www.wikidata.org/entity/Q30877299

description

2009 nî lūn-bûn

@nan

2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年学术文章

@wuu

2009年学术文章

@zh-cn

2009年学术文章

@zh-hans

2009年学术文章

@zh-my

2009年学术文章

@zh-sg

2009年學術文章

@yue

name

ALDH1A2 (RALDH2) genetic variation in human congenital heart disease.

@ast

ALDH1A2 (RALDH2) genetic variation in human congenital heart disease.

@en

type

label

ALDH1A2 (RALDH2) genetic variation in human congenital heart disease.

@ast

ALDH1A2 (RALDH2) genetic variation in human congenital heart disease.

@en

prefLabel

ALDH1A2 (RALDH2) genetic variation in human congenital heart disease.

@ast

ALDH1A2 (RALDH2) genetic variation in human congenital heart disease.

@en

P1433

Q30877299-49E21E17-D3AB-480A-8C55-B5018E909D20

P1476

Q30877299-9B55FFCD-AE2E-454D-9594-494F6FEC891A

P2093

Q30877299-027EC3B5-A603-465C-BED6-6EEAFADC0BF5

Q30877299-04BB2E36-5321-45C0-B3A3-C944F97A5749

Q30877299-0A3AEC7A-3D22-45EA-B9A2-EEF44AE380D1

Q30877299-508E7EEB-7D03-410D-B7D9-BF3E30FEB5ED

Q30877299-56FEBE57-592B-43F3-9BF2-1DFA4FF4077D

Q30877299-762CB2BE-8226-476E-AC7D-FA09D683BF23

Q30877299-87C9B247-7E3B-4C2A-AB9B-BA5AA043C04C

Q30877299-A56FB398-34B6-45AA-91D8-4A5F8716D0E3

Q30877299-DF5E74B3-0543-450C-9BE2-73DFF067C1CF

Q30877299-F32491F0-91C7-49C1-A52C-AA4815CFECDB

P2860

Q30877299-0574F1D5-B199-4EEF-AED2-2E7EE18ED323

Q30877299-069D97D5-4DF5-41D7-8E36-4F3C19181939

Q30877299-0BFB5901-189A-452A-B441-B210B140A049

Q30877299-0F678DB9-5B0F-4949-9153-3CD85988E31E

Q30877299-133681F1-E530-4000-BD2B-5020A68A7BDD

Q30877299-17B4D770-63CA-4E22-ADB5-21D1F41672CF

Q30877299-1998EAC3-FDBC-4FAE-B784-3245762DF766

Q30877299-1EF440ED-6C3B-4773-BF0D-3374E0304343

Q30877299-21B646C3-B8EB-46A4-A0D3-BB8AB6338A10

Q30877299-267B1672-178C-4D6C-921E-F64A78167ABC

P2888

Q30877299-85E463B1-9038-4489-BED3-0425D3D9B31C

P304

Q30877299-9285F7FB-6C8A-4F8C-AF99-4B1A0BA7DBD4

P31

Q30877299-DF85CE61-ACCF-4052-B96B-1370CAC9C498

P356

Q30877299-C33A6AA3-1F1F-47C8-A3C1-74291A76888A

P478

Q30877299-C06008EB-F652-4F78-84D8-31810C990F14

P50

Q30877299-1754517E-063A-449B-AFFB-9B9A800A930C

Q30877299-30D8366C-CE30-407B-B0DF-71646CDF3DB7

Q30877299-9A36D96C-64B0-4F4C-B5A0-B9C3CC873CA8

P577

Q30877299-E91B8366-4CDD-4163-B1D1-82DD66EAAA38

P5875

Q30877299-211ACA8E-0781-46B3-AED3-4BD07CE07D01

P6179

Q30877299-02F69F3D-42B0-49E4-B41F-AD765BBE9434

P698

Q30877299-175058AD-E406-44B5-AB05-63A6F83833D0

P921

Q30877299-16C5EFD8-6C52-4FD3-8CA0-9D213F1F71C5

P932

Q30877299-45D10F19-B4D9-485D-A01D-AABFB43C3FB3

P356

1471-2350-10-113

P1433

BMC Medical Genetics

P1476

ALDH1A2 (RALDH2) genetic variation in human congenital heart disease

@en

P2093

Alexandre C Pereira

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

Fábio A Silva

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

José Xavier-Neto

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

Lívia P Marques

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

Marilene Pavan

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

Michelle Vasconcelos

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

Paulo S Oliveira

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

Roberta M Cravo

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

Sonia M F Mesquita

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

Viviane F Ruiz

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

P2860

Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2

Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes

The neighbor-joining method: a new method for reconstructing phylogenetic trees

PROCHECK: a program to check the stereochemical quality of protein structures

The structure of retinal dehydrogenase type II at 2.7 A resolution: implications for retinal specificity

Structure of mitochondrial aldehyde dehydrogenase: the genetic component of ethanol aversion

Sheep liver cytosolic aldehyde dehydrogenase: the structure reveals the basis for the retinal specificity of class 1 aldehyde dehydrogenases

The Amber biomolecular simulation programs

P2888

1471-2350-10-113

P304

113

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

P31

scholarly article

P356

10.1186/1471-2350-10-113

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

P478

10

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

P50

José Eduardo Krieger

Antonio Augusto Lopes

Tiago P Sobreira

P577

2009-11-03T00:00:00Z

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

P5875

38065011

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

P6179

1033822695

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

P698

19886994

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

P921

P932

2779186

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