Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mai Baalbaki"'
Autor:
Teresa Kortz, Mai Baalbaki, Chayse Jones, Raya Mussa, Joel Manyahi, Hendry Sawe, Michael Matthay
Publikováno v:
Critical Care Medicine. 51:314-314
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecc93401edff45b0e2aaac44b893c51a
https://doi.org/10.1097/01.ccm.0000908328.66018.6c
https://doi.org/10.1097/01.ccm.0000908328.66018.6c
Autor:
Jun Zou, Diana Tran, Mai Baalbaki, Ling Fung Tang, Annie Poon, Angelo Pelonero, Erron W Titus, Christiana Yuan, Chenxu Shi, Shruthi Patchava, Elizabeth Halper, Jasmine Garg, Irina Movsesyan, Chaoying Yin, Roland Wu, Lisa D Wilsbacher, Jiandong Liu, Ronald L Hager, Shaun R Coughlin, Martin Jinek, Clive R Pullinger, John P Kane, Daniel O Hart, Pui-Yan Kwok, Rahul C Deo
Publikováno v:
eLife, Vol 4 (2015)
Truncating mutations in the giant sarcomeric protein Titin result in dilated cardiomyopathy and skeletal myopathy. The most severely affected dilated cardiomyopathy patients harbor Titin truncations in the C-terminal two-thirds of the protein, sugges
Externí odkaz:
https://doaj.org/article/64ef752df04c4b96ab2dff639a70afb6
Autor:
Akiko Hata, Xuan Jiang, Daniel O. Hart, Jamie McDonald, Melissa Sandoval, Mai Baalbaki, Giorgio Lagna, Whitney Wooderchak-Donahue, Shaun R. Coughlin, Pinar Bayrak-Toydemir, Hilary Clay, Prajakta Ghatpande
Publikováno v:
Science signaling, vol 11, iss 513
Jiang, Xuan; Wooderchak-Donahue, Whitney L; McDonald, Jamie; Ghatpande, Prajakta; Baalbaki, Mai; Sandoval, Melissa; et al.(2018). Inactivating mutations in Drosha mediate vascular abnormalities similar to hereditary hemorrhagic telangiectasia.. Science signaling, 11(513), eaan6831-eaan6831. doi: 10.1126/scisignal.aan6831. UCSF: Retrieved from: http://www.escholarship.org/uc/item/1mh2x7w0
Jiang, Xuan; Wooderchak-Donahue, Whitney L; McDonald, Jamie; Ghatpande, Prajakta; Baalbaki, Mai; Sandoval, Melissa; et al.(2018). Inactivating mutations in Drosha mediate vascular abnormalities similar to hereditary hemorrhagic telangiectasia.. Science signaling, 11(513), eaan6831-eaan6831. doi: 10.1126/scisignal.aan6831. UCSF: Retrieved from: http://www.escholarship.org/uc/item/1mh2x7w0
The transforming growth factor–β (TGF-β) and bone morphogenetic protein (BMP) family of cytokines critically regulates vascular morphogenesis and homeostasis. Impairment of TGF-β or BMP signaling leads to heritable vascular disorders, including
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f93f32bb541c3db26147892261c6c90
https://escholarship.org/uc/item/1mh2x7w0
https://escholarship.org/uc/item/1mh2x7w0
Autor:
Erron W. Titus, Roland S. Wu, Clive R. Pullinger, Annie Poon, Chenxu Shi, Irina Movsesyan, Jiandong Liu, Christiana Yuan, Mai Baalbaki, Jun Zou, John P. Kane, Shruthi Patchava, Ronald L. Hager, Ling Fung Tang, Chaoying Yin, Pui-Yan Kwok, Martin Jinek, Diana Tran, Shaun R. Coughlin, Lisa D. Wilsbacher, Rahul C. Deo, Daniel O. Hart, Jasmine Garg, Angelo Pelonero, Elizabeth Halper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74bd3a7343db637081a2c4a78e3d2890
https://doi.org/10.7554/elife.09406.025
https://doi.org/10.7554/elife.09406.025
Autor:
David Jones, Mai Baalbaki, Anna-Pavlina Haramis, Nullin Divecha, Yvette Stijf-Bultsma, Wolfgang Fischle, Daniel Hart, Panagiota Giardoglou, Lilly Sommer, Maria Tauber, Shannon Lauberth, Kathy Gelato
Publikováno v:
The FASEB Journal. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1b1735a81034b280859a7a8b698fc68
https://doi.org/10.1096/fasebj.29.1_supplement.90.2
https://doi.org/10.1096/fasebj.29.1_supplement.90.2
Autor:
Ling Fung Tang, Angelo Pelonero, Christiana Yuan, Chenxu Shi, Mai Baalbaki, Shaun R. Coughlin, Erron W. Titus, Ronald L. Hager, Annie Poon, Jasmine Garg, Lisa D. Wilsbacher, Clive R. Pullinger, Pui-Yan Kwok, Chaoying Yin, Daniel O. Hart, Roland S. Wu, Rahul C. Deo, Elizabeth Halper, Shruthi Patchava, Martin Jinek, Diana Tran, Jun Zou, John P. Kane, Irina Movsesyan, Jiandong Liu
Publikováno v:
eLife
eLife, Vol 4 (2015)
eLife, Vol 4 (2015)
Truncating mutations in the giant sarcomeric protein Titin result in dilated cardiomyopathy and skeletal myopathy. The most severely affected dilated cardiomyopathy patients harbor Titin truncations in the C-terminal two-thirds of the protein, sugges
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf3ddd548e60b95ee344eadd0a83c767
https://doi.org/10.5167/uzh-118340
https://doi.org/10.5167/uzh-118340
Autor:
Jiang, Xuan, Wooderchak-Donahue, Whitney L., McDonald, Jamie, Ghatpande, Prajakta, Baalbaki, Mai, Sandoval, Melissa, Hart, Daniel, Clay, Hilary, Coughlin, Shaun, Lagna, Giorgio, Bayrak-Toydemir, Pinar, Hata, Akiko
Publikováno v:
Science Signaling; 1/16/2018, Vol. 11 Issue 513, p1-N.PAG, 13p
Autor:
Kortz, Teresa, Baalbaki, Mai, Jones, Chayse, Mussa, Raya, Manyahi, Joel, Sawe, Hendry, Matthay, Michael
Publikováno v:
Critical Care Medicine; 2023 Supplement, Vol. 51, p314-314, 1p