(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