检索结果 - Patel, Vipulkumar

Early detection of metabolic dysregulation using water T(2) analysis of biobanked samples 由 Mishra, Ina, Jones, Clinton, Patel, Vipulkumar, Deodhar, Sneha, Cistola, David P

获取全文 获取全文 获取全文

Radiofrequency Ablation, Where It Stands in Interventional Radiology Today 由 Patel, Vipulkumar, Ritchie, Charles A., Padula, Carlos, McKinney, J. Mark

获取全文 获取全文 获取全文

Diffusion Tensor Imaging of Forearm Nerves in Humans 由 Zhou, Yuxiang, Kumaravel, Manickam, Patel, Vipulkumar S, Sheikh, Kazim A, Narayana, Ponnada A

获取全文 获取全文 获取全文

Aptamer-based search for correlates of plasma and serum water T(2): implications for early metabolic dysregulation and metabolic syndrome 由 Patel, Vipulkumar, Dwivedi, Alok K., Deodhar, Sneha, Mishra, Ina, Cistola, David P.

获取全文 获取全文 获取全文

High Resolution Diffusion Tensor Imaging of Human Nerves in Forearm 由 Zhou, Yuxiang, Narayana, Ponnada A, Kumaravel, Manickam, Athar, Parveen, Patel, Vipulkumar S, Sheikh, Kazim A

获取全文 获取全文 获取全文

Neuropsychological, Neurovirological and Neuroimmune Aspects of Abnormal GABAergic Transmission in HIV Infection 由 Buzhdygan, Tetyana, Lisinicchia, Joshua, Patel, Vipulkumar, Johnson, Kenneth, Neugebauer, Volker, Paessler, Slobodan, Jennings, Kristofer, Gelman, Benjamin

获取全文 获取全文 获取全文

Novel functions of CCM1 delimit the relationship of PTB/PH domains 由 Zhang, Jun, Dubey, Pallavi, Padarti, Akhil, Zhang, Aileen, Patel, Rinkal, Patel, Vipulkumar, Cistola, David, Badr, Ahmed

获取全文 获取全文 获取全文

Investigation of a Bicyclo[1.1.1]pentane as a Phenyl Replacement within an LpPLA(2) Inhibitor 由 Measom, Nicholas D., Down, Kenneth D., Hirst, David J., Jamieson, Craig, Manas, Eric S., Patel, Vipulkumar K., Somers, Don O.

获取全文 获取全文 获取全文

Water T(2) as an early, global and practical biomarker for metabolic syndrome: an observational cross-sectional study 由 Robinson, Michelle D., Mishra, Ina, Deodhar, Sneha, Patel, Vipulkumar, Gordon, Katrina V., Vintimilla, Raul, Brown, Kim, Johnson, Leigh, O’Bryant, Sid, Cistola, David P.

获取全文 获取全文 获取全文

Differential recognition of HIV-stimulated IL-1β and IL-18 secretion through NLR and NAIP signalling in monocyte-derived macrophages 由 Triantafilou, Kathy, Ward, Christopher J. K., Czubala, Magdalena, Ferris, Robert G., Koppe, Emma, Haffner, Curt, Piguet, Vincent, Patel, Vipulkumar K., Amrine-Madsen, Heather, Modis, Louise K., Masters, Seth L., Triantafilou, Martha

获取全文 获取全文 获取全文

Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal Diagnosis 由 Vossaert, Liesbeth, Wang, Qun, Salman, Roseen, McCombs, Anne K., Patel, Vipulkumar, Qu, Chunjing, Mancini, Michael A., Edwards, Dean P., Malovannaya, Anna, Liu, Pengfei, Shaw, Chad A., Levy, Brynn, Wapner, Ronald J., Bi, Weimin, Breman, Amy M., Van den Veyver, Ignatia B., Beaudet, Arthur L.

获取全文 获取全文 获取全文

Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder 由 Normand, Elizabeth A., Braxton, Alicia, Nassef, Salma, Ward, Patricia A., Vetrini, Francesco, He, Weimin, Patel, Vipulkumar, Qu, Chunjing, Westerfield, Lauren E., Stover, Samantha, Dharmadhikari, Avinash V., Muzny, Donna M., Gibbs, Richard A., Dai, Hongzheng, Meng, Linyan, Wang, Xia, Xiao, Rui, Liu, Pengfei, Bi, Weimin, Xia, Fan, Walkiewicz, Magdalena, Van den Veyver, Ignatia B., Eng, Christine M., Yang, Yaping

获取全文 获取全文 获取全文

Retrospective analysis of a clinical exome sequencing cohort reveals the mutational spectrum and identifies candidate disease-associated loci for BAFopathies 由 Chen, Chun-An, Lattier, John, Zhu, Wenmiao, Rosenfeld, Jill, Wang, Lei, Scott, Tiana M., Du, Haowei, Patel, Vipulkumar, Dang, Anh, Magoulas, Pilar, Streff, Haley, Sebastian, Jessica, Svihovec, Shayna, Curry, Kathryn, Delgado, Mauricio R., Hanchard, Neil, Lalani, Seema, Marom, Ronit, Madan-Khetarpal, Suneeta, Saenz, Margarita, Dai, Hongzheng, Meng, Linyan, Xia, Fan, Bi, Weimin, Liu, Pengfei, Posey, Jennifer E., Scott, Daryl A., Lupski, James R., Eng, Christine M., Xiao, Rui, Yuan, Bo

获取全文 获取全文 获取全文

De Novo Missense Variants in TRAF7 Cause Developmental Delay, Congenital Anomalies, and Dysmorphic Features 由 Tokita, Mari J., Chen, Chun-An, Chitayat, David, Macnamara, Ellen, Rosenfeld, Jill A., Hanchard, Neil, Lewis, Andrea M., Brown, Chester W., Marom, Ronit, Shao, Yunru, Novacic, Danica, Wolfe, Lynne, Wahl, Colleen, Tifft, Cynthia J., Toro, Camilo, Bernstein, Jonathan A., Hale, Caitlin L., Silver, Julia, Hudgins, Louanne, Ananth, Amitha, Hanson-Kahn, Andrea, Shuster, Shirley, Magoulas, Pilar L., Patel, Vipulkumar N., Zhu, Wenmiao, Chen, Stella M., Jiang, Yanjun, Liu, Pengfei, Eng, Christine M., Batkovskyte, Dominyka, di Ronza, Alberto, Sardiello, Marco, Lee, Brendan H., Schaaf, Christian P., Yang, Yaping, Wang, Xia

获取全文 获取全文 获取全文

Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies 由 Yuan, Bo, Neira, Juanita, Pehlivan, Davut, Santiago-Sim, Teresa, Song, Xiaofei, Rosenfeld, Jill, Posey, Jennifer E., Patel, Vipulkumar, Jin, Weihong, Adam, Margaret P., Baple, Emma L., Dean, John, Fong, Chin-To, Hickey, Scott E., Hudgins, Louanne, Leon, Eyby, Madan-Khetarpal, Suneeta, Rawlins, Lettie, Rustad, Cecilie F., Stray-Pedersen, Asbjørg, Tveten, Kristian, Wenger, Olivia, Diaz, Jullianne, Jenkins, Laura, Martin, Laura, McGuire, Marianne, Pietryga, Marguerite, Ramsdell, Linda, Slattery, Leah, Abid, Farida, Bertuch, Alison, Grange, Dorothy, Immken, LaDonna, Schaaf, Christian P., Van Esch, Hilde, Bi, Weimin, Cheung, Sau Wai, Breman, Amy M., Smith, Janice L., Shaw, Chad, Crosby, Andrew H., Eng, Christine, Yang, Yaping, Lupski, James R., Xiao, Rui, Liu, Pengfei

获取全文 获取全文 获取全文