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BMPR2‐expressing bone marrow‐derived endothelial‐like progenitor cells alleviate pulmonary arterial hypertension in vivo.
Published in:
Respirology, 2019, v. 24, n. 11, p. 1095, doi. 10.1111/resp.13552
By:
- Harper, Rebecca L.;
- Maiolo, Suzanne;
- Ward, Rebekah J.;
- Seyfang, Jemma;
- Cockshell, Michaelia P.;
- Bonder, Claudine S.;
- Reynolds, Paul N.
Publication type:
Article
Development of vascular disease models to explore disease causation and pathomechanisms of rare vascular diseases.
Published in:
Seminars in Immunopathology, 2022, v. 44, n. 3, p. 259, doi. 10.1007/s00281-022-00925-9
By:
- Harper, Rebecca L.;
- Ferrante, Elisa A.;
- Boehm, Manfred
Publication type:
Article
Reduced FOXF1 links unrepaired DNA damage to pulmonary arterial hypertension.
Published in:
Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-43039-y
By:
- Isobe, Sarasa;
- Nair, Ramesh V.;
- Kang, Helen Y.;
- Wang, Lingli;
- Moonen, Jan-Renier;
- Shinohara, Tsutomu;
- Cao, Aiqin;
- Taylor, Shalina;
- Otsuki, Shoichiro;
- Marciano, David P.;
- Harper, Rebecca L.;
- Adil, Mir S.;
- Zhang, Chongyang;
- Lago-Docampo, Mauro;
- Körbelin, Jakob;
- Engreitz, Jesse M.;
- Snyder, Michael P.;
- Rabinovitch, Marlene
Publication type:
Article
Mast cell activation and degranulation in acute artery injury: A target for post‐operative therapy.
Published in:
FASEB Journal, 2023, v. 37, n. 7, p. 1, doi. 10.1096/fj.202201745RR
By:
- Harper, Rebecca L.;
- Fang, Fang;
- San, Hong;
- Negro, Alejandra;
- St. Hilaire, Cynthia;
- Yang, Dan;
- Chen, Guibin;
- Yu, Zhen;
- Dmitrieva, Natalia I.;
- Lanzer, Jan;
- Davaine, Jean‐Michel;
- Schwartzbeck, Robin;
- Walts, Avram D.;
- Kovacic, Jason C.;
- Boehm, Manfred
Publication type:
Article
BMPR2 gene therapy for PAH acts via Smad and non- Smad signalling.
Published in:
Respirology, 2016, v. 21, n. 4, p. 727, doi. 10.1111/resp.12729
By:
- Harper, Rebecca L.;
- Reynolds, Ann M.;
- Bonder, Claudine S.;
- Reynolds, Paul N.
Publication type:
Article
BMPR2 gene delivery reduces mutation-related PAH and counteracts TGF-β-mediated pulmonary cell signalling.
Published in:
Respirology, 2016, v. 21, n. 3, p. 526, doi. 10.1111/resp.12712
By:
- Feng, Feng;
- Harper, Rebecca L;
- Reynolds, Paul N
Publication type:
Article
iPSC–endothelial cell phenotypic drug screening and in silico analyses identify tyrphostin-AG1296 for pulmonary arterial hypertension.
Published in:
Science Translational Medicine, 2021, v. 13, n. 592, p. 1, doi. 10.1126/scitranslmed.aba6480
By:
- Gu, Mingxia;
- Donato, Michele;
- Guo, Minzhe;
- Wary, Neil;
- Miao, Yifei;
- Mao, Shuai;
- Saito, Toshie;
- Otsuki, Shoichiro;
- Wang, Lingli;
- Harper, Rebecca L.;
- Sa, Silin;
- Khatri, Purvesh;
- Rabinovitch, Marlene
Publication type:
Article

Found: 7

BMPR2‐expressing bone marrow‐derived endothelial‐like progenitor cells alleviate pulmonary arterial hypertension in vivo.

Development of vascular disease models to explore disease causation and pathomechanisms of rare vascular diseases.

Reduced FOXF1 links unrepaired DNA damage to pulmonary arterial hypertension.

Mast cell activation and degranulation in acute artery injury: A target for post‐operative therapy.

BMPR2 gene therapy for PAH acts via Smad and non- Smad signalling.

BMPR2 gene delivery reduces mutation-related PAH and counteracts TGF-β-mediated pulmonary cell signalling.

iPSC–endothelial cell phenotypic drug screening and in silico analyses identify tyrphostin-AG1296 for pulmonary arterial hypertension.