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of 3
pro vyhledávání: '"Reina Yu"'
Autor:
Reina Yu, Adel A. Rashad, Cameron F. Abrams, Irwin Chaiken, Bibek Parajuli, Brendon Ngo, Kriti Acharya
Publikováno v:
Biochemistry. 55(44)
We recently reported the discovery of a recombinant chimera, denoted DAVEI (dual-acting virucidal entry inhibitor), which is able to selectively cause specific and potent lytic inactivation of both pseudotyped and fully infectious human immunodeficie
Autor:
Monkol Lek, Samir H Al-Mueilo, Alhusain J. Alzahrani, Kelly A. Thomas, Dimitri S. Monos, Daniel G. MacArthur, Elena Carrigan, Ajay K. Israni, Eyas Mukhtar, Konrad J. Karczewski, Shefali S. Verma, Marylyn D. Ritchie, Brendan J. Keating, Hui Gao, Teresa Webster, Malek Kamoun, Ana Gonzalez, Jessica van Setten, Paul I.W. de Bakker, Laura Steel, Aubree Himes, Kim M. Olthoff, Pamala A. Jacobson, Maede Mohebnasab, Barbara Murphy, Kelsey M. Llyod, Hareesh R. Chandrupatla, Suganthi Balasubramanian, Takesha Lee, James Snyder, Abhinav Gangasani, Baolin Wu, B. Chang, Weihua Guan, Yun Li, Folkert W. Asselbergs, Kelly A. Birdwell, Matthew B. Lanktree, Abraham Shaked, Andrew Pasquier, Cisca Wijmenga, Cuiping Hou, Abigail Colasacco, Chanel Wong, Yontao Lu, Daniel E. McGinn, William S. Oetting, Fahad Al-Muhanna, Amein K. Al-Ali, Abdullah Akdere, Michael B. Miller, Jacob van Houten, David S. Schladt, Hongzhi Cao, Abdullah M. Al-Rubaish, Randy Phillips, Vinicius Tragante, Hakon Hakonarson, Nikhil Nair, Pablo García-Pavía, James Garifallou, Toumy Guettouche, Zach Michaud, Michael V. Holmes, Tiancheng Wang, Reina Yu
Publikováno v:
Li, Y R, van Setten, J, Verma, S S, Lu, Y, Holmes, M V, Gao, H, Lek, M, Nair, N, Chandrupatla, H, Chang, B, Karczewski, K J, Wong, C, Mohebnasab, M, Mukhtar, E, Phillips, R, Tragante, V, Hou, C, Steel, L, Lee, T, Garifallou, J, Guettouche, T, Cao, H, Guan, W, Himes, A, van Houten, J, Pasquier, A, Yu, R, Carrigan, E, Miller, M B, Schladt, D, Akdere, A, Gonzalez, A, Llyod, K M, McGinn, D, Gangasani, A, Michaud, Z, Colasacco, A, Snyder, J, Thomas, K, Wang, T, Wu, B, Alzahrani, A J, Al-Ali, A K, Al-Muhanna, F A, Al-Rubaish, A M, Al-Mueilo, S, Monos, D S, Murphy, B, Olthoff, K M, Wijmenga, C, Webster, T, Kamoun, M, Balasubramanian, S, Lanktree, M B, Oetting, W S, Garcia-Pavia, P, MacArthur, D G, de Bakker, P I W, Hakonarson, H, Birdwell, K A, Jacobson, P A, Ritchie, M D, Asselbergs, F W, Israni, A K, Shaked, A & Keating, B J 2015, ' Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies ', Genome Medicine, vol. 7, 90 . https://doi.org/10.1186/s13073-015-0211-x
Genome medicine, 7:90. BMC
Genome Medicine, 7(1). BioMed Central
Genome Medicine
Genome medicine, 7:90. BMC
Genome Medicine, 7(1). BioMed Central
Genome Medicine
Background In addition to HLA genetic incompatibility, non-HLA difference between donor and recipients of transplantation leading to allograft rejection are now becoming evident. We aimed to create a unique genome-wide platform to facilitate genomic
Publikováno v:
Acta Médica del Centro, Vol 6, Iss 4, Pp 97-101 (2012)
Steinert'scongenital myotonic dystrophy is a hereditary disease with a pattern of dominant autosomal inheritance that has broad forms of presentation and can occur from early life to adulthood. It presents with diverse symptoms including: respiratory
Externí odkaz:
https://doaj.org/article/92068a0073504d4b8b5aa9df8007263b