Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Gabriella L Robertson"'
Autor:
Dina Simkin, Kelly A Marshall, Carlos G Vanoye, Reshma R Desai, Bernabe I Bustos, Brandon N Piyevsky, Juan A Ortega, Marc Forrest, Gabriella L Robertson, Peter Penzes, Linda C Laux, Steven J Lubbe, John J Millichap, Alfred L George Jr, Evangelos Kiskinis
Publikováno v:
eLife, Vol 10 (2021)
Mutations in KCNQ2, which encodes a pore-forming K+ channel subunit responsible for neuronal M-current, cause neonatal epileptic encephalopathy, a complex disorder presenting with severe early-onset seizures and impaired neurodevelopment. The conditi
Externí odkaz:
https://doaj.org/article/77a9457c95724ba991f9276aa4d1ab55
Autor:
Connor J. Beebout, Gabriella L. Robertson, Bradley I. Reinfeld, Alexandra M. Blee, Grace H. Morales, John R. Brannon, Walter J. Chazin, W. Kimryn Rathmell, Jeffrey C. Rathmell, Vivian Gama, Maria Hadjifrangiskou
Publikováno v:
Nat Microbiol
Urinary tract infections are among the most common human bacterial infections and place a significant burden on healthcare systems due to associated morbidity, cost, and antibiotic use. Despite being a facultative anaerobe, uropathogenic Escherichia
Autor:
Gabriella L. Robertson, Stellan Riffle, Mira Patel, Caroline Bodnya, Andrea Marshall, Heather K. Beasley, Edgar Garza-Lopez, Jianqiang Shao, Zer Vue, Antentor Hinton, Maria S. Stoll, Sholto de Wet, Rensu P. Theart, Ram Prosad Chakrabarty, Ben Loos, Navdeep S. Chandel, Jason A. Mears, Vivian Gama
Publikováno v:
Journal of Cell Science. 136
Mitochondria and peroxisomes are dynamic signaling organelles that constantly undergo fission, driven by the large GTPase dynamin-related protein 1 (DRP1; encoded by DNM1L). Patients with de novo heterozygous missense mutations in DNM1L present with
Autor:
Andrew R. Patterson, Gabriel A. Needle, Ayaka Sugiura, Channing Chi, KayLee K. Steiner, Emilie L. Fisher, Gabriella L. Robertson, Caroline Bodnya, Janet G. Markle, Vivian Gama, Jeffrey C. Rathmell
Publikováno v:
bioRxiv
SUMMARYInborn Errors of Metabolism (IEM) and Immunity (IEI) are Mendelian diseases in which complex phenotypes and patient rarity can limit clinical annotations. Few genes are assigned to both IEM and IEI, but immunometabolic demands suggest function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d03e22ef76f827ee75ea22de50a86e49
https://doi.org/10.1101/2023.01.24.525419
https://doi.org/10.1101/2023.01.24.525419
Autor:
Gabriella L. Robertson, Stellan Riffle, Mira Patel, Andrea Marshall, Heather Beasley, Edgar Garza Lopez, Jianqiang Shao, Zer Vue, Maria S. Stoll, Sholto de Wet, Rensu P. Theart, Ben Loos, Antentor Hinton, Jason A. Mears, Vivian Gama
Mitochondria and peroxisomes are both dynamic signaling organelles that constantly undergo fission. While mitochondrial fission is known to coordinate cellular metabolism, proliferation, and apoptosis, the physiological relevance of peroxisome dynami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6f69be0c8bc178ab0722c9bf247c111
https://doi.org/10.1101/2021.12.31.474637
https://doi.org/10.1101/2021.12.31.474637
Publikováno v:
Cell Metab
Mitochondrial plasticity is a key regulator of cell fate decisions. Mitochondrial division involves Dynamin-related protein-1 (Drp1) oligomerization, which constricts membranes at endoplasmic reticulum (ER) contact sites. The mechanisms driving the f
Autor:
Reshma R. Desai, John Millichap, Kelly A Marshall, Evangelos Kiskinis, Gabriella L Robertson, Marc P. Forrest, Linda Laux, Dina Simkin, Alfred L. George, Peter Penzes, Steven J. Lubbe, Bernabé I. Bustos, Juan A. Ortega, Brandon N Piyevsky, Carlos G. Vanoye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0bf16ea33ef217dbd275aa0d951f319
https://doi.org/10.7554/elife.64434.sa2
https://doi.org/10.7554/elife.64434.sa2
Autor:
Steven J. Lubbe, Gabriella L Robertson, Carlos G. Vanoye, Reshma R. Desai, Peter Penzes, John Millichap, Evangelos Kiskinis, Bernabé I. Bustos, Kelly A Marshall, Dina Simkin, Brandon N Piyevsky, Alfred L. George, Juan A. Ortega, Linda Laux, Marc P. Forrest
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
eLife
eLife, Vol 10 (2021)
Universidad de Barcelona
eLife
eLife, Vol 10 (2021)
Mutations in KCNQ2, which encodes a pore-forming K+ channel subunit responsible for neuronal M-current, cause neonatal epileptic encephalopathy, a complex disorder presenting with severe early-onset seizures and impaired neurodevelopment. The conditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bb3f591130ed352737002c9c4ded72b
http://hdl.handle.net/2445/185597
http://hdl.handle.net/2445/185597
Autor:
Alejandra I. Romero-Morales, Gabriella L. Robertson, Anuj Rastogi, Megan L. Rasmussen, Hoor Temuri, Gregory Scott McElroy, Ram Prosad Chakrabarty, Lawrence Hsu, Paula M. Almonacid, Bryan A. Millis, Navdeep S. Chandel, Jean-Philippe Cartailler, Vivian Gama
Summary Leigh syndrome (LS) is a rare, inherited neuro-metabolic disorder that presents with bilateral brain lesions. This disease is caused by defects in the mitochondrial respiratory chain and associated nuclear-encoded proteins. We generated induc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37a35740bdd821b8fc49a0328eef92ba
Autor:
Vivian Gama, Megan L. Rasmussen, Bjorn C. Knollmann, Stellan N. Riffle, Lili Wang, Linzheng Shi, Dylan T. Burnette, Nilay Taneja, Abigail C. Neininger, Gabriella L. Robertson
Publikováno v:
iScience
iScience, Vol 23, Iss 4, Pp-(2020)
iScience, Vol 23, Iss 4, Pp-(2020)
Summary MCL-1 is a well-characterized inhibitor of cell death that has also been shown to be a regulator of mitochondrial dynamics in human pluripotent stem cells. We used cardiomyocytes derived from human-induced pluripotent stem cells (hiPSC-CMs) t