VEGF C2578A polymorphism does not contribute to amyotrophic lateral sclerosis susceptibility in sporadic Chinese patients (Q45246507)

11 December 2017

VEGF C2578A polymorphism does not contribute to amyotrophic lateral sclerosis susceptibility in sporadic Chinese patients (English)

1 reference

amyotrophic lateral sclerosis

11 December 2017

0 references

author name string

Yingshuang Zhang

1

1 reference

11 December 2017

Huagang Zhang

2

1 reference

11 December 2017

Yu Fu

3

1 reference

11 December 2017

Hongsong Song

4

1 reference

11 December 2017

Liping Wang

5

1 reference

11 December 2017

Jun Zhang

6

1 reference

11 December 2017

Dongsheng Fan

7

1 reference

11 December 2017

1 June 2006

1 reference

Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

11 December 2017

1 reference

11 December 2017

7

1 reference

11 December 2017

2

1 reference

11 December 2017

119-122

1 reference

Natural history of amyotrophic lateral sclerosis in a database population. Validation of a scoring system and a model for survival prediction.

11 December 2017

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Mice lacking the CNTF receptor, unlike mice lacking CNTF, exhibit profound motor neuron deficits at birth

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Alternative splicing of the 5'-sequences of the mouse EAAT2 glutamate transporter and expression in a transgenic model for amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Extra neurofilament NF-L subunits rescue motor neuron disease caused by overexpression of the human NF-H gene in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

A novel candidate region for ALS on chromosome 14q11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Therapies in amyotrophic lateral sclerosis-beyond riluzole.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Novel polymorphisms in the promoter and 5' UTR regions of the human vascular endothelial growth factor gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

VEGF promoter haplotype and amyotrophic lateral sclerosis (ALS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Mechanisms of angiogenesis and arteriogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Vascular endothelial growth factor (VEGF) stimulates neurogenesis in vitro and in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Assignment of the vascular endothelial growth factor gene to human chromosome 6p21.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Surviving ischemia: adaptive responses mediated by hypoxia-inducible factor 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Analysis of chromosome 5q13 genes in amyotrophic lateral sclerosis: Homozygous naip deletion in a sporadic case

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Amyotrophic lateral sclerosis: current understanding.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Screening of AP endonuclease as a candidate gene for amyotrophic lateral sclerosis (ALS)

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Potential role of LIF as a modifier gene in the pathogenesis of amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Mutation screening of manganese superoxide dismutase in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Polymorphisms of the vascular endothelial growth factor and susceptibility to diabetic microvascular complications in patients with type 1 diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

Favorable effect of VEGF gene transfer on ischemic peripheral neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600600657

10.1080/14660820600600657

21 January 2018

Identifiers

DOI

1 reference

11 December 2017

1 reference