Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Stacy, Caillier"'
Autor:
Kristen J. Wade, Rayo Suseno, Kerry Kizer, Jacqueline Williams, Juliano Boquett, Stacy Caillier, Nicholas R. Pollock, Adam Renschen, Adam Santaniello, Jorge R. Oksenberg, Paul J. Norman, Danillo G. Augusto, Jill A. Hollenbach
Publikováno v:
Genome Biology, Vol 25, Iss 1, Pp 1-23 (2024)
Abstract The extremely high levels of genetic polymorphism within the human major histocompatibility complex (MHC) limit the usefulness of reference-based alignment methods for sequence assembly. We incorporate a short-read, de novo assembly algorith
Externí odkaz:
https://doaj.org/article/da420c82ac434ddc86e06bc9431d32c9
Autor:
Brooke Rhead, Xiaorong Shao, Jennifer S. Graves, Tanuja Chitnis, Amy T. Waldman, Timothy Lotze, Teri Schreiner, Anita Belman, Lauren Krupp, Benjamin M. Greenberg, Bianca Weinstock–Guttman, Gregory Aaen, Jan M. Tillema, Moses Rodriguez, Janace Hart, Stacy Caillier, Jayne Ness, Yolanda Harris, Jennifer Rubin, Meghan S. Candee, Mark Gorman, Leslie Benson, Soe Mar, Ilana Kahn, John Rose, T. Charles Casper, Hong Quach, Diana Quach, Catherine Schaefer, Emmanuelle Waubant, Lisa F. Barcellos, the US Network of Pediatric MS Centers
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 6, Pp 1053-1061 (2019)
Abstract Objective Onset of multiple sclerosis (MS) occurs in childhood for approximately 5% of cases (pediatric MS, or ped‐MS). Epigenetic influences are strongly implicated in MS pathogenesis in adults, including the contribution from microRNAs (
Externí odkaz:
https://doaj.org/article/7e4b193be7ec429facf7230a6a5acd9e
Autor:
Leonardo M. Amorim, Danillo G. Augusto, Neda Nemat-Gorgani, Gonzalo Montero-Martin, Wesley M. Marin, Hengameh Shams, Ravi Dandekar, Stacy Caillier, Peter Parham, Marcelo A. Fernández-Viña, Jorge R. Oksenberg, Paul J. Norman, Jill A. Hollenbach
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
The KIR (killer-cell immunoglobulin-like receptor) region is characterized by structural variation and high sequence similarity among genes, imposing technical difficulties for analysis. We undertook the most comprehensive study to date of KIR geneti
Externí odkaz:
https://doaj.org/article/aa5a1107c343415581b1d8b8a30fec56
Autor:
Silvia Rossi, Valeria Studer, Alessandro Moscatelli, Caterina Motta, Giancarlo Coghe, Giuseppe Fenu, Stacy Caillier, Fabio Buttari, Francesco Mori, Francesca Barbieri, Maura Castelli, Valentina De Chiara, Fabrizia Monteleone, Raffaele Mancino, Giorgio Bernardi, Sergio E Baranzini, Maria G Marrosu, Jorge R Oksenberg, Diego Centonze
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e67357 (2013)
Synaptic transmission and plasticity mediated by NMDA receptors (NMDARs) could modulate the severity of multiple sclerosis (MS). Here the role of NMDARs in MS was first explored in 691 subjects carrying specific allelic variants of the NR1 subunit ge
Externí odkaz:
https://doaj.org/article/ac849ca193ad4a9c8c5893d2677a3459
Autor:
Bruce A C, Cree, Pierre-Antoine, Gourraud, Jorge R, Oksenberg, Carolyn, Bevan, Elizabeth, Crabtree-Hartman, Jeffrey M, Gelfand, Douglas S, Goodin, Jennifer, Graves, Ari J, Green, Ellen, Mowry, Darin T, Okuda, Daniel, Pelletier, H-Christian, von Büdingen, Scott S, Zamvil, Alisha, Agrawal, Stacy, Caillier, Caroline, Ciocca, Refujia, Gomez, Rachel, Kanner, Robin, Lincoln, Antoine, Lizee, Pamela, Qualley, Adam, Santaniello, Leena, Suleiman, Monica, Bucci, Valentina, Panara, Nico, Papinutto, William A, Stern, Alyssa H, Zhu, Gary R, Cutter, Sergio, Baranzini, Roland G, Henry, Stephen L, Hauser
Publikováno v:
Annals of Neurology
Objective To characterize the accrual of long‐term disability in a cohort of actively treated multiple sclerosis (MS) patients and to assess whether clinical and magnetic resonance imaging (MRI) data used in clinical trials have long‐term prognos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73cff46e688bcc50e28a7735b32ba7e7
https://pubmed.ncbi.nlm.nih.gov/27464262
https://pubmed.ncbi.nlm.nih.gov/27464262
Autor:
Maria, Ban, Stacy, Caillier, Inger-Lise, Mero, Kjell-Morten, Myhr, Elisabeth G, Celius, Jan, Aarseth, Øivind, Torkildsen, Hanne F, Harbo, Jorge, Oksenberg, Stephen L, Hauser, Stephen, Sawcer, Alastair, Compston
Publikováno v:
Annals of neurology. 73(3)
An association has previously been reported between susceptibility to multiple sclerosis and the rare mutant alleles of the CYP27B1 gene responsible for autosomal recessive vitamin D-dependent rickets type 1 (VDDR1). In an attempt to replicate this f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::89b36ec916668313a10be8285cdfbc57
https://pubmed.ncbi.nlm.nih.gov/23444327
https://pubmed.ncbi.nlm.nih.gov/23444327