(Q48406327)

English

A novel mutation in the HTRA1 gene identified in Chinese CARASIL pedigree.

scientific article published on 20 August 2012

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6493480

A novel mutation in the HTRA1 gene identified in Chinese CARASIL pedigree. (English)

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6493480

author name string

Xiao-Ling Wang

1

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6493480

Chuan-Fen Li

2

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6493480

Hong-Wei Guo

3

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6493480

Bing-Zhen Cao

4

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6493480

publication date

20 August 2012

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6493480

CNS Neuroscience & Therapeutics

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6493480

18

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6493480

10

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6493480

867-869

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6493480

Cerebral arterial pathology of CADASIL and CARASIL (Maeda syndrome).

1 reference

https://pubmed.ncbi.nlm.nih.gov/22900900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Chinese pedigree of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): clinical and radiological features.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22900900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22900900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular pathogenesis of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/22900900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A missense HTRA1 mutation expands CARASIL syndrome to the Caucasian population

1 reference

https://pubmed.ncbi.nlm.nih.gov/22900900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): from discovery to gene identification

1 reference

https://pubmed.ncbi.nlm.nih.gov/22900900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mutation in the HTRA1 gene causes CARASIL without alopecia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22900900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The structural basis of mode of activation and functional diversity: a case study with HtrA family of serine proteases

1 reference

https://pubmed.ncbi.nlm.nih.gov/22900900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial young-adult-onset arteriosclerotic leukoencephalopathy with alopecia and lumbago without arterial hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/22900900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial unusual encephalopathy of Binswanger's type without hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/22900900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1111/J.1755-5949.2012.00373.X

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6493480

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6493480

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

2 July 2019

http://europepmc.org/abstract/PMC/6493480

ResearchGate publication ID

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