Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Mehdi, Keddache"'
Autor:
Chirayu Goswami, Michael Sheldon, Christian Bixby, Mehdi Keddache, Alexander Bogdanowicz, Yihe Wang, Jonathan Schultz, Jessica McDevitt, James LaPorta, Elaine Kwon, Steven Buyske, Dana Garbolino, Glenys Biloholowski, Alex Pastuszak, Mary Storella, Amit Bhalla, Florence Charlier-Rodriguez, Russ Hager, Robin Grimwood, Shareef A. Nahas
Publikováno v:
BMC Infectious Diseases, Vol 22, Iss 1, Pp 1-12 (2022)
Abstract Background The Centers for Disease Control and Prevention contracted with laboratories to sequence the SARS-CoV-2 genome from positive samples across the United States to enable public health officials to investigate the impact of variants o
Externí odkaz:
https://doaj.org/article/e8bee7780dda4d538db015dfa1fe10c0
Autor:
Nathan Salomonis, Phillip J. Dexheimer, Larsson Omberg, Robin Schroll, Stacy Bush, Jeffrey Huo, Lynn Schriml, Shannan Ho Sui, Mehdi Keddache, Christopher Mayhew, Shiva Kumar Shanmukhappa, James Wells, Kenneth Daily, Shane Hubler, Yuliang Wang, Elias Zambidis, Adam Margolin, Winston Hide, Antonis K. Hatzopoulos, Punam Malik, Jose A. Cancelas, Bruce J. Aronow, Carolyn Lutzko
Publikováno v:
Stem Cell Reports, Vol 7, Iss 1, Pp 110-125 (2016)
The rigorous characterization of distinct induced pluripotent stem cells (iPSC) derived from multiple reprogramming technologies, somatic sources, and donors is required to understand potential sources of variability and downstream potential. To achi
Externí odkaz:
https://doaj.org/article/7257d13864d04b54a5863b5373af033d
Autor:
Chirayu Goswami, Michael Sheldon, Christian Bixby, Mehdi Keddache, Alexander Bogdanowicz, Yihe Wang, Jonathan Schultz, Jessica McDevitt, James LaPorta, Elaine Kwon, Steven Buyske, Dana Garbolino, Glenys Biloholowski, Alex Pastuszak, Mary Storella, Amit Bhalla, Florence Charlier-Rodriguez, Russ Hager, Robin Grimwood, Shareef Amin Nahas
Background The Centers for Disease Control and Prevention contracted with laboratories to sequence the SARS-CoV-2 genome from positive samples across the United States to enable public health officials to investigate the impact of variants on disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf391492e2ba2996fbed7ceba2c02ccd
https://doi.org/10.21203/rs.3.rs-1134436/v1
https://doi.org/10.21203/rs.3.rs-1134436/v1
Autor:
Nupur Dasgupta, You-Hai Xu, Sunghee Oh, Ying Sun, Li Jia, Mehdi Keddache, Gregory A Grabowski
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e74912 (2013)
Gaucher disease type 1, an inherited lysosomal storage disorder, is caused by mutations in GBA1 leading to defective glucocerebrosidase (GCase) function and consequent excess accumulation of glucosylceramide/glucosylsphingosine in visceral organs. En
Externí odkaz:
https://doaj.org/article/3906fe1689964fcda5bef74993202cc5
Autor:
Muhammad Tariq, Thanh-Tam Le, Patrick Putnam, Steven Kindel, Mehdi Keddache, Stephanie M. Ware
Publikováno v:
Cardiogenetics, Vol 2, Iss 1, Pp e7-e7 (2012)
Pediatric cardiomyopathy is a genetically heterogeneous disease associated with significant morbidity. Although identification of underlying etiology is important for management, therapy, and screening of at risk family members, molecular diagnosis i
Externí odkaz:
https://doaj.org/article/559b6dbb7f6144e78ec72a5578381b5f
Autor:
Rachel Sheridan, Kristin Lampe, Shiva Kumar Shanmukhappa, Patrick Putnam, Mehdi Keddache, Senad Divanovic, Jorge Bezerra, Kasper Hoebe
Publikováno v:
PLoS ONE, Vol 6, Iss 7, p e21979 (2011)
Using a small scale ENU mutagenesis approach we identified a recessive germline mutant, designated Lampe1 that exhibited growth retardation and spontaneous hepatosteatosis. Low resolution mapping based on 20 intercrossed Lampe1 mice revealed linkage
Externí odkaz:
https://doaj.org/article/33e71703d69d4f61ae6f46f632937462
Autor:
Valerie P. O’Brien, Shlomo Shinnar, Avital Cnaan, Deborah Hirtz, Tracy A. Glauser, Katherine D. Holland, Dennis J. Dlugos, Peggy Clark, Mehdi Keddache, Lisa J. Martin, Gregory A. Grabowski
Publikováno v:
Annals of Neurology. 81:444-453
Objective To determine whether common polymorphisms in CACNA1G, CACNA1H, CACNA1I, and ABCB1 are associated with differential short-term seizure outcome in childhood absence epilepsy (CAE). Methods Four hundred forty-six CAE children in a randomized d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::293c18c37c8ec4fed5562fcbe5d32c99
https://doi.org/10.1002/ana.24886
https://doi.org/10.1002/ana.24886
Autor:
Phillip J. Dexheimer, Kristine S. Vogel, Kwangmin Choi, Hilde Brems, Jianqiang Wu, Eric Legius, Jose A. Cancelas, Yanan Yu, Mehdi Keddache, Margaret R. Wallace, Lisa J. Martin, Paul R. Andreassen, Nancy Ratner, Robert J. Spinner
Publikováno v:
Acta Neuropathol
In Neurofibromatosis type 1, NF1 gene mutations in Schwann cells (SC) drive benign plexiform neurofibroma (PNF), and no additional SC changes explain patient-to-patient variability in tumor number. Evidence from twin studies suggests that variable ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a289fee013eaecff21fbe2891c7fceef
https://pubmed.ncbi.nlm.nih.gov/31664505
https://pubmed.ncbi.nlm.nih.gov/31664505
Autor:
Shiva Kumar Shanmukhappa, Jeffrey S. Huo, Adam A. Margolin, Shane L. Hubler, Punam Malik, Robin Schroll, Carolyn Lutzko, Elias T. Zambidis, James A. Wells, Kenneth Daily, Winston Hide, Christopher N. Mayhew, Stacy Bush, Yuliang Wang, Bruce J. Aronow, Nathan Salomonis, Phillip J. Dexheimer, Mehdi Keddache, Antonis K. Hatzopoulos, Shannan J. Ho Sui, Jose A. Cancelas, Larsson Omberg, Lynn M. Schriml
Publikováno v:
Stem Cell Reports, Vol 7, Iss 1, Pp 110-125 (2016)
Stem Cell Reports
Stem Cell Reports
Summary The rigorous characterization of distinct induced pluripotent stem cells (iPSC) derived from multiple reprogramming technologies, somatic sources, and donors is required to understand potential sources of variability and downstream potential.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2412ef7349e985fd1fbcbacb59c03f9
Autor:
Johannes Christiaan Maria van der Loo, Mehdi Keddache, Paritha Arumugam, Michael A. Goodman, Dennis D. Hickstein, Danielle Lynn, Phillip J. Dexheimer, Anastacia Loberg, Mohammed Nasimuzzaman, Devin Pillis, David W. Russell, Punam Malik, Thomas R. Bauer
Publikováno v:
Journal of virology. 92(1)
Strong viral enhancers in gammaretrovirus vectors have caused cellular proto-oncogene activation and leukemia, necessitating the use of cellular promoters in “enhancerless” self-inactivating integrating vectors. However, cellular promoters result
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::759ff39dabe4087e2778bef3f265441f
https://pubmed.ncbi.nlm.nih.gov/29046446
https://pubmed.ncbi.nlm.nih.gov/29046446