Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Marissa K. Cooper"'
Autor:
Akito Nakagawa, Marissa K. Cooper, Maria Kost-Alimova, James Berstler, Binglan Yu, Lorenzo Berra, Elizabeth S. Klings, Mary S. Huang, Matthew M. Heeney, Donald B. Bloch, Warren M. Zapol
Publikováno v:
ACS Omega. 7:14009-14016
Sickle cell disease (SCD) is an inherited disorder of hemoglobin (Hb); approximately 300,000 babies are born worldwide with SCD each year. In SCD, fibers of polymerized sickle Hb (HbS) form in red blood cells (RBCs), which cause RBCs to develop their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e95d2ae3e779781fcb4bdc7494aa1a1
https://doi.org/10.1021/acsomega.2c00541
https://doi.org/10.1021/acsomega.2c00541
Autor:
Rajeev Malhotra, Bryn Reinstadler, Aranya Bagchi, Daniel Bloch, Hardik Shah, Fumito Ichinose, Robert M. H. Grange, Eizo Marutani, Gregory R. Wojtkiewicz, Vamsi K. Mootha, Marissa K. Cooper, Yusuke Miyazaki, Grigorij Schleifer, Allyson G. Hindle, Akito Nakagawa, Warren M. Zapol, Olga Goldberger, Rohit Sharma, Annabelle Batten
Publikováno v:
Molecular Genetics and Metabolism. 133:83-93
Leigh syndrome is a severe mitochondrial neurodegenerative disease with no effective treatment. In the Ndufs4−/− mouse model of Leigh syndrome, continuously breathing 11% O2 (hypoxia) prevents neurodegeneration and leads to a dramatic extension (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b8dfb0c48990bb2740cda981f0aec86
https://doi.org/10.1016/j.ymgme.2021.03.005
https://doi.org/10.1016/j.ymgme.2021.03.005
Autor:
Robert M H, Grange, Rohit, Sharma, Hardik, Shah, Bryn, Reinstadler, Olga, Goldberger, Marissa K, Cooper, Akito, Nakagawa, Yusuke, Miyazaki, Allyson G, Hindle, Annabelle J, Batten, Gregory R, Wojtkiewicz, Grigorij, Schleifer, Aranya, Bagchi, Eizo, Marutani, Rajeev, Malhotra, Donald B, Bloch, Fumito, Ichinose, Vamsi K, Mootha, Warren M, Zapol
Publikováno v:
Mol Genet Metab
Leigh syndrome is a severe mitochondrial neurodegenerative disease with no effective treatment. In the Ndufs4(−/−) mouse model of LS, continuously breathing 11% O(2) (hypoxia) prevents neurodegeneration and leads to a dramatic extension (~5-fold)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0267752dcaa19019458cf3a795f5b069
https://pubmed.ncbi.nlm.nih.gov/33752971
https://pubmed.ncbi.nlm.nih.gov/33752971
Autor:
Daniel Bloch, Warren M. Zapol, Michele Ferrari, Marissa K. Cooper, Qiukan Chen, Elizabeth S. Klings, Lorenzo Berra, Binglan Yu, Faik N. Musayev, Grigorij Schleifer, Martin K. Safo, Akito Nakagawa, Osheiza Abdulmalik, Ronni S. Safo, Chen Liu
Publikováno v:
Molecular Pharmaceutics
Sickle cell disease is an inherited disorder of hemoglobin (Hb). During a sickle cell crisis, deoxygenated sickle hemoglobin (deoxyHbS) polymerizes to form fibers in red blood cells (RBCs), causing the cells to adopt “sickled” shapes. Using small
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2224b7a18f3c187e92c40826977f83e
http://europepmc.org/articles/PMC5942180
http://europepmc.org/articles/PMC5942180