A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. - Wikidata - awgldk - TriplyDB

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.

http://www.wikidata.org/entity/Q33481614

about

Heart Disease and Stroke Statistics--2013 Update: A Report From the American Heart Association Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma Characterization of nuclear localization and SUMOylation of the ATBF1 transcription factor in epithelial cells Emerging directions in the genetics of atrial fibrillation Stroke genetics: prospects for personalized medicine Genome-wide association studies of late-onset cardiovascular disease Aberrant sodium influx causes cardiomyopathy and atrial fibrillation in mice 2014 AHA/ACC/HRS guideline for the management of patients with atrial fibrillation: a report of the American College of Cardiology/American Heart Association Task Force on practice guidelines and the Heart Rhythm Society.Genetic susceptibility to cerebrovascular disease Genetic Risk Factors for Ischemic and Hemorrhagic Stroke A rare variant in MYH6 is associated with high risk of sick sinus syndrome Genetic mutations in African patients with atrial fibrillation: Rationale and design of the Study of Genetics of Atrial Fibrillation in an African Population (SIGNAL)Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.Heart disease and stroke statistics--2014 update: a report from the American Heart Association Heart disease and stroke statistics--2012 update: a report from the American Heart Association Heart Disease and Stroke Statistics-2017 Update: A Report From the American Heart Association Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2 Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.Targeted deep sequencing reveals no definitive evidence for somatic mosaicism in atrial fibrillation.No Additional Prognostic Value of Genetic Information in the Prediction of Vascular Events after Cerebral Ischemia of Arterial Origin: The PROMISe Study.Deletion of atbf1/zfhx3 in mouse prostate causes neoplastic lesions, likely by attenuation of membrane and secretory proteins and multiple signaling pathways.Genetic susceptibility to ischemic stroke.Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis Whole Exome Sequencing in Atrial Fibrillation.Personalized management of atrial fibrillation: Proceedings from the fourth Atrial Fibrillation competence NETwork/European Heart Rhythm Association consensus conference.Unravelling the genetics of ischaemic stroke.Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies.Lone atrial fibrillation: does it exist?Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese.Relation of Obstructive Sleep Apnea and a Common Variant at Chromosome 4q25 to Atrial Fibrillation.Genetic Investigation Into the Differential Risk of Atrial Fibrillation Among Black and White Individuals.Pitx2, an atrial fibrillation predisposition gene, directly regulates ion transport and intercalated disc genes.Decoding the complex genetic causes of heart diseases using systems biology Identification of six polymorphisms as novel susceptibility loci for ischemic or hemorrhagic stroke by exome-wide association studies.Epigenome-wide association of myocardial infarction with DNA methylation sites at loci related to cardiovascular disease.The environmental epidemiology of atrial arrhythmogenesis Severity of obstructive sleep apnea influences the effect of genotype on response to anti-arrhythmic drug therapy for atrial fibrillation.A contemporary review on the genetic basis of atrial fibrillation.A Potential Role of Esophageal Cancer Related Gene-4 for Atrial Fibrillation.

P2860

Q22306356-42412E5B-CBD7-4F7C-922E-0917A53A36BD Q24263464-E8750149-1107-4298-8D29-BDCB80B2D64C Q24339436-12D256CF-834D-42A5-985B-A0D845D16B61 Q26852051-CAC452BE-9DDC-4590-8325-EB0A5AB4C255 Q27006885-04DEDACD-7EC2-4B19-B0A5-042F832F83E8 Q27012711-19EEB826-479C-4EC2-B404-52BEEEB8A551 Q27329882-F462ED85-6A4E-4198-965B-51B133181D5B Q27341873-56D19937-B391-4514-9069-65B87068BB42 Q28076438-34352F95-D8B6-45B7-81E1-991DD936C592 Q28079249-B84A906B-CE58-4BD6-9B68-2D9E414FAFFF Q28306661-38A8313B-06EE-4559-8242-7A541A339E3E Q28607469-6C98EBA7-F6E8-4172-9519-81876064DDE7 Q29417025-AD834A8C-EB3B-421E-B9DA-95DF8CCEAABD Q29417129-6BA9E6F6-9DF8-46B6-8C92-086C27EE11C6 Q29547691-C524D1C3-7AB0-46F8-B136-0B0C1385A041 Q29547909-A673E01F-434A-40E5-B68E-3CDFCB2601A4 Q30238784-A6667327-BBCE-433A-803C-A7C24BFA69A6 Q30354370-172FACF5-ECD7-4FAC-9EA3-823F4A8050EB Q30356365-FE10D9C4-E8DB-46E7-B179-46DC8DB398F3 Q30392171-D481D603-0496-4B4A-AF20-900DD0DBE570 Q30405365-E14556B5-740A-441D-AE16-4D9C74690319 Q30410016-08296CE5-9F8F-4D0C-9F57-9D07E7B00739 Q30414709-D839AEA1-5237-489A-B58F-18D0867CD727 Q30430623-E5D75352-8638-47B1-B11E-19F12005D2F9 Q30489794-780B0923-755B-407C-A72B-0B983C1CEFAD Q30663685-FCBAADF9-EE69-405D-AA71-42BA11969A6C Q33538069-68AB8EB8-0AEC-466B-8A9F-CCE272899A44 Q33553928-A854D26E-FCAF-44E0-9F9D-13E127BA9D40 Q33560948-44A8D705-9255-4D0D-89D4-36AADDE95938 Q33563000-E19FF715-8514-42EE-ABAB-7E3FFE5D0363 Q33566207-8EA85049-B560-478F-93F5-94038823A765 Q33574112-9E10B212-2319-470E-8EA9-B8583383DB33 Q33580059-F1DDAB66-A2F5-48C6-A4F6-0D2228AA2D9E Q33639681-DC768A54-342B-4CCE-83D7-F11AC36DCA62 Q33675091-EB089F56-1156-41A9-9BB3-40D1DC88F603 Q33691392-EE0835A7-5CC4-49E0-AC45-2049922ED99E Q33703467-5B4F7017-23E0-4A88-9758-C1AABFCE51E6 Q33714490-0FB9A16A-4AFA-41C4-8630-85551626D558 Q33732880-145879AE-C4DE-4FBE-B260-A1AF663ABAC5 Q33758744-C87864B9-975E-4B31-9478-ADAEFBB916D3

P2860

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.

http://www.wikidata.org/entity/Q33481614

description

2009 nî lūn-bûn

@nan

2009 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

A sequence variant in ZFHX3 on ...... rillation and ischemic stroke.

@ast

A sequence variant in ZFHX3 on ...... rillation and ischemic stroke.

@en

type

label

A sequence variant in ZFHX3 on ...... rillation and ischemic stroke.

@ast

A sequence variant in ZFHX3 on ...... rillation and ischemic stroke.

@en

prefLabel

A sequence variant in ZFHX3 on ...... rillation and ischemic stroke.

@ast

A sequence variant in ZFHX3 on ...... rillation and ischemic stroke.

@en

P1433

Q33481614-EFAAB986-9FCA-4D2B-B674-7772BDC387C6

P1476

Q33481614-A3D0D6AE-F8E6-4C9F-8FEF-6BC215B958BA

P2093

Q33481614-1202FF00-7D5E-41F9-A52C-BD64595C96C5

Q33481614-1AAA1C14-8EED-45CD-98A5-673037F52DEC

Q33481614-21CB7D9E-91B2-4CA2-8476-ACE61A6EC1A0

Q33481614-36F70FF9-AA7F-4AFC-9EDF-4B43F8A7108A

Q33481614-3F1DCD5C-6370-43BE-A173-DB58E6C4F644

Q33481614-3FFA555B-AFE9-4528-8480-479074A69B9D

Q33481614-4F539F30-3E46-45AC-809D-F82A5BAF9024

Q33481614-5452ED72-DD06-4101-9919-FF82DA34A500

Q33481614-575F2A14-27D7-4767-B6F9-B42A7626B837

Q33481614-618F55BB-FE06-4518-9C49-15E3D1AFEF92

P2860

Q33481614-1DBFC424-8A69-4A38-9515-8BE67F54D734

Q33481614-2E94EECD-FC1E-455F-92DE-13E37A7F611B

Q33481614-2EA97DFE-F646-4276-A336-7CAE64DB470E

Q33481614-49E3977D-3CD8-4B96-B018-430C2B07A86E

Q33481614-BC913D54-2010-48B1-8234-68E680E549C3

Q33481614-C707F6A3-C080-4AFD-B96A-B7491BAF8AA2

P2888

Q33481614-C163392D-08F1-4AF5-B2D9-09465C9D729B

P304

Q33481614-F6BADF82-1851-41C9-9B61-49B9C351BA7C

P31

Q33481614-CBE96542-E618-4EBB-8B14-40DC3662BE29

P356

Q33481614-D61B65B7-7436-4BBF-9965-3ABB2CB219B1

P407

Q33481614-8429D281-0A0F-4185-89AC-2F0599DC8EC4

P433

Q33481614-D1A2E1ED-589A-499A-9EF8-B41CB37C6D01

P478

Q33481614-94E8AB2C-3539-42BC-8C6A-F7DA9DAEC21B

P50

Q33481614-0C118F5F-F196-4653-91AA-298255615104

Q33481614-2F57392A-7C16-4AD9-A85B-9D89F3F4784D

Q33481614-3563D7EC-79EE-468D-B13B-E1056146E4B1

Q33481614-3695D893-C54C-4791-ABF7-FC096B10433A

Q33481614-49116D49-2671-4549-B163-2E05BCB0D68E

Q33481614-639545FA-CA6A-44F3-AD72-2936945C404D

Q33481614-70176960-7780-4349-BD4F-F7519CCBF030

Q33481614-82FE8664-DC13-4447-A9BB-264EE549929B

Q33481614-8579D242-9A3A-4092-A8CC-C85DF2CE5BA0

Q33481614-88F6A9DF-EEE3-42E1-993C-CBF3E0EE436B

P577

Q33481614-6846B4A4-3DA1-4A23-84EA-3DCAA4DFBEBF

P5875

Q33481614-3AFCEC0F-7B82-4C67-9A09-5CCD640F357A

P698

Q33481614-588B28E6-2CE7-4D82-8E7B-A6AF8AE7F510

P921

Q33481614-A5F6A3CD-EB09-449E-A2F3-2F0BFEC3DFF1

P932

Q33481614-90F6365C-F2BF-464D-B95D-EB24A8E54B3F

P356

P1433

Nature Genetics

P1476

A sequence variant in ZFHX3 on ...... rillation and ischemic stroke.

@en

P2093

Audhild Nyrnes

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

Dan Roden

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

David O Arnar

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

E Bernd Ringelstein

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

Einar M Valdimarsson

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

Ellisiv B Mathiesen

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

Erin M Hald

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

G Bragi Walters

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

Gayle Kucera

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

Gregor Kuhlenbäumer

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

P2860

Positive and negative regulation of myogenic differentiation of C2C12 cells by isoforms of the multiple homeodomain zinc finger transcription factor ATBF1

A human alpha-fetoprotein enhancer-binding protein, ATBF1, contains four homeodomains and seventeen zinc fingers

Variants conferring risk of atrial fibrillation on chromosome 4q25.

Lifetime risk for development of atrial fibrillation: the Framingham Heart Study.

Antithrombotic treatment in atrial fibrillation.

Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke.

P2888

P304

876-878

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

P31

scholarly article

P356

10.1038/NG.417

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

P407

P433

8

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

P478

41

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

P50

Christian Gieger

Gudmar Thorleifsson

Unnur Þorsteinsdóttir

Inger Njølstad

Daniel F Gudbjartsson

Martin Dichgans

Solveig Gretarsdottir

P577

2009-07-13T00:00:00Z

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

P5875

26666141

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

P698

19597491

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

P921

atrial fibrillation

P932

2740741

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