KALRN Rare and Common Variants and Susceptibility to Ischemic Stroke in Chinese Han Population (Q41007600)

25 September 2017

KALRN Rare and Common Variants and Susceptibility to Ischemic Stroke in Chinese Han Population (English)

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25 September 2017

Meizheng Dang

1

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25 September 2017

Zhenzhen Wang

2

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25 September 2017

Ruyou Zhang

3

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25 September 2017

Xiaoying Li

4

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25 September 2017

Yanqing Peng

5

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25 September 2017

Xuesong Han

6

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25 September 2017

Litao Sun

7

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25 September 2017

Jiawei Tian

8

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25 September 2017

28 April 2015

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25 September 2017

NeuroMolecular Medicine

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25 September 2017

17

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25 September 2017

3

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25 September 2017

241-250

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https://scigraph.springernature.com/pub.10.1007/s12017-015-8352-z

25 September 2017

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cites work

Rare variant association analysis methods for complex traits

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Kalirin-7, a protein enriched in postsynaptic density, is involved in ischemic signal transduction.

21 January 2018

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Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12017-015-8352-Z

Common and rare variants in multifactorial susceptibility to common diseases

21 January 2018

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Renalase gene polymorphisms in patients with type 2 diabetes, hypertension and stroke

21 January 2018

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Control of interneuron dendritic growth through NRG1/erbB4-mediated kalirin-7 disinhibition

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12017-015-8352-Z

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12017-015-8352-Z

Scaffold protein X11α interacts with kalirin-7 in dendrites and recruits it to Golgi outposts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12017-015-8352-Z

Kalirin: a novel genetic risk factor for ischemic stroke.

21 January 2018

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Stroke in China: epidemiology, prevention, and management strategies

21 January 2018

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Gene variants associated with ischemic stroke: the cardiovascular health study

21 January 2018

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Kalirin, a key player in synapse formation, is implicated in human diseases

21 January 2018

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Variants within the nitric oxide synthase 1 gene are associated with stroke susceptibility.

21 January 2018

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Functional SNP of ARHGEF10 confers risk of atherothrombotic stroke

21 January 2018

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Severity of coronary atherosclerosis and stroke incidence in 7-year follow-up

21 January 2018

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The variant rs8048002 T>C in intron 3 of the MHC2TA gene is associated with risk of developing acute coronary syndrome.

21 January 2018

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Association of the suppressor of cytokine signaling 1 (SOCS1) gene polymorphisms with acute coronary syndrome in Mexican patients.

21 January 2018

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Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease

21 January 2018

1 reference

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Kalirin promotes neointimal hyperplasia by activating Rac in smooth muscle cells

21 January 2018

1 reference

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An association study on renalase polymorphisms and ischemic stroke in a Chinese population

21 January 2018

1 reference

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Lack of association between genetic variations in the KALRN region and ischemic stroke

21 January 2018

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12 December 2020

Kalirin-9 and Kalirin-12 Play Essential Roles in Dendritic Outgrowth and Branching

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12 December 2020

Overexpression of inducible nitric oxide synthase by neointimal smooth muscle cells

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12 December 2020

A functional polymorphism at miR-491-5p binding site in the 3'-UTR of MMP-9 gene confers increased risk for atherosclerotic cerebral infarction in a Chinese population

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12 December 2020

Una nueva guía de la Organización Mundial de la Salud y la Sociedad Internacional de Hipertensión para el manejo de la hipertensión arterial: hacia la guía común

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12 December 2020

Familial aggregation of coronary heart disease and its relation to known genetic risk factors

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12 December 2020

Family history as an independent risk factor for coronary artery disease

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12 December 2020

10.1007/S12017-015-8352-Z

Identifiers

DOI

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25 September 2017

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