Výsledky vyhledávání - Patel, Vipulkumar

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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