Risultati della ricerca - Patel, Vipulkumar

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

Differential recognition of HIV-stimulated IL-1β and IL-18 secretion through NLR and NAIP signalling in monocyte-derived macrophages di 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

Testo Testo Testo

Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal Diagnosis di 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.

Testo Testo Testo

Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder di 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

Testo Testo Testo

Retrospective analysis of a clinical exome sequencing cohort reveals the mutational spectrum and identifies candidate disease-associated loci for BAFopathies di 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

Testo Testo Testo

De Novo Missense Variants in TRAF7 Cause Developmental Delay, Congenital Anomalies, and Dysmorphic Features di 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

Testo Testo Testo

Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies di 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

Testo Testo Testo