Autologous correction in patient induced pluripotent stem cell‐endothelial cells to identify a novel pathogenic mutation of hereditary hemorrhagic telangiectasia-Reference-Cited by-同舟云学术

Autologous correction in patient induced pluripotent stem cell‐endothelial cells to identify a novel pathogenic mutation of hereditary hemorrhagic telangiectasia

Published:2020-10 Issue:4 Volume:10 Page:1-11
ISSN:2045-8940
Container-title:Pulmonary Circulation
language:en
Short-container-title:Pulm. circ.

Author:

Zhou Fang¹^ORCID,Zhao Xiuli²,Liu Xiu³,Liu Yanyan¹,Ma Feng⁴⁵,Liu Bao³,Yang Jun¹⁶^ORCID

Affiliation:

1. Department of Cell BiologyChinese Academy of Medical Sciences and School of Basic MedicineBeijingChina

2. Department of GeneticsChinese Academy of Medical Sciences and School of Basic MedicineBeijingChina

3. Department of Vascular SurgeryChinese Academy of Medical Science and Peking Union Medical CollegeBeijingChina

4. State Key Laboratory of Experimental HematologyInstitute of Hematology & Blood Diseases HospitalTianjinChina

5. Institute of Blood TransfusionChinese Academy of Medical Sciences & Peking Union Medical CollegeChengduChina

6. Department of PhysiologyZhejiang UniversitySchool of MedicineHangzhouZhejiangChina

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1177/2045894019885357

Reference40 articles.

1. Screening for children from families with Rendu‐Osler‐Weber disease: from geneticist to clinician;Giordano P;J Thromb Haemost,2006

2. Prevalence of pulmonary arteriovenous malformations (PAVMs) and occurrence of neurological symptoms in patients with hereditary haemorrhagic telangiectasia (HHT);Kjeldsen AD;J Intern Med,2000

3. Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers;Sabba C;J Thromb Haemost,2007

4. Endoglin, a TGF‐beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1;McAllister KA;Nat Genet,1994

5. A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12;Johnson DW;Genome Res,1995

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Human iPSCs as Model Systems for BMP-Related Rare Diseases;Cells;2023-09-02

2. The vascular niche in next generation microphysiological systems;Lab on a Chip;2021