Targeted Gene Delivery Of Bmpr2 Attenuates Pulmonary Hypertension

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Targeted gene delivery of BMPR2 attenuates pulmonary ...

    https://erj.ersjournals.com/content/39/2/329
    Feb 01, 2012 · BMPR2 is predominantly expressed on pulmonary endothelium and has complex interactions with transforming growth factor (TGF)-β signalling mechanisms. Our objectives were to assess the effect on PAH of upregulating BMPR2 by targeted adenoviral BMPR2 gene delivery to the pulmonary vascular endothelium.Author: A. M. Reynolds, M. D. Holmes, M. D. Holmes, Sergei M. Danilov, P. N. Reynolds, P. N. Reynolds

(PDF) Targeted gene delivery of BMPR2 attenuates pulmonary ...

    https://www.researchgate.net/publication/51475337_Targeted_gene_delivery_of_BMPR2_attenuates_pulmonary_hypertension
    Targeted gene delivery of BMPR2 attenuates pulmonary hypertension Article (PDF Available) in European Respiratory Journal 39(2):329-43 · July 2011 with 41 Reads How we measure 'reads'

Targeted gene delivery of BMPR2

    https://erj.ersjournals.com/content/erj/39/2/329.full.pdf
    Targeted gene delivery of BMPR2 attenuates pulmonary hypertension A.M. Reynolds*,#, M.D. Holmes*,#,", S.M. Danilov+,1 and P.N. Reynolds*,#," ABSTRACT: Pulmonary arterial hypertension (PAH) remains a fatal disease despite modern pharmacotherapy. Mutations in the gene for bone morphogenetic protein receptor type II (BMPR2)Author: A. M. Reynolds, M. D. Holmes, M. D. Holmes, Sergei M. Danilov, P. N. Reynolds, P. N. Reynolds

Selective enhancement of endothelial BMPR-II with BMP9 ...

    https://www.nature.com/articles/nm.3877
    Jun 15, 2015 · BMP9 activates signaling through the BMPR-II receptor in endothelial cells and reverses established disease in three animal models of pulmonary hypertension, thus pointing to a potential new ...Author: Lu Long, Mark Leonard Ormiston, XuDong Yang, Mark Southwood, Stefan Andreas Gräf, Rajiv D Machado, M...

MicroRNA-140-5p and SMURF1 regulate pulmonary arterial ...

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4922709/
    Jul 01, 2016 · Loss of the growth-suppressive effects of bone morphogenetic protein (BMP) signaling has been demonstrated to promote pulmonary arterial endothelial cell dysfunction and induce pulmonary arterial smooth muscle cell (PASMC) proliferation, leading to the development of pulmonary arterial hypertension (PAH).Author: Alexander M.K. Rothman, Nadine D. Arnold, Josephine A. Pickworth, James Iremonger, Loredana Ciuclan,...

811. ACE-Targeted eNOS and BMPR2 Gene Therapy Attenuates ...

    https://www.researchgate.net/publication/31957811_811_ACE-Targeted_eNOS_and_BMPR2_Gene_Therapy_Attenuates_Pulmonary_Hypertension_in_a_Chronic_Hypoxia_Rat_Model
    ACE-Targeted eNOS and BMPR2 Gene Therapy Attenuates Pulmonary Hypertension in a Chronic Hypoxia Rat Model ... that BMPR2 gene delivery attenuated the …

Targeted gene delivery of BMPR2 attenuates pulmonary ...

    http://core.ac.uk/display/12793062
    BMPR2 is predominantly expressed on pulmonary endothelium and has complex interactions with transforming growth factor (TGF)-b signalling mechanisms. Our objectives were to assess the effect on PAH of upregulating BMPR2 by targeted adenoviral BMPR2 gene …

FK506 activates BMPR2, rescues ... - PubMed Central (PMC)

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3726153/
    Aug 01, 2013 · Furthermore, patients with a BMPR2 mutation have worse pulmonary vascular remodeling . The importance of BMPR2 dysfunction in PAH is supported by studies in transgenic mice. Mice with deletion of BMPR2 in ECs develop PAH, as do mice expressing a dominant-negative Bmpr2 gene after birth in vascular SMCs .Author: Edda Spiekerkoetter, Xuefei Tian, Jie Cai, Rachel K. Hopper, Deepti Sudheendra, Caiyun G. Li, Nesrin...

[Full text] Paeoniflorin Ameliorates Chronic Hypoxia ...

    https://www.dovepress.com/paeoniflorin-ameliorates-chronic-hypoxiasu5416-induced-pulmonary-arter-peer-reviewed-fulltext-article-DDDT
    BMPR2 and its related signaling pathway have been recognized as a key regulator of pulmonary vascular homeostasis, as an estimated 80% of familial and 20% of idiopathic PAH patients carrying a heterozygous BMPR2 mutation. 28,29 BMPR2 gene mutations have also been found in patients with pulmonary hypertension caused by other factors (congenital ...Author: Min Yu, Liyao Peng, Ping Liu, Mingxia Yang, Hong Zhou, Yirui Ding, Jingjing Wang, Wen Huang, Qi Tan,...

BMPR2‐expressing bone marrow‐derived endothelial‐like ...

    https://onlinelibrary.wiley.com/doi/full/10.1111/resp.13552
    INTRODUCTION. Pulmonary arterial hypertension (PAH) is a devastating disease and despite available therapeutics, median survival remains at 3–5 years after diagnosis. 1 The disease is characterized by increased pulmonary resistance due to vascular remodelling. Mutations in the bone morphogenetic protein receptor type 2 (BMPR2), leading to reduced receptor expression, are strongly associated ...Author: Rebecca L. Harper, Rebecca L. Harper, Suzanne Maiolo, Suzanne Maiolo, Rebekah J. Ward, Jemma Seyfang...

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