نتائج البحث - Rangasamy, Sampathkumar

Molecular Intricacies and the Role of ER Stress in Diabetes حسب Balasubramanyam, Muthuswamy, Singh, Lalit P., Rangasamy, Sampathkumar

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Diabetic Retinopathy and Inflammation: Novel Therapeutic Targets حسب Rangasamy, Sampathkumar, McGuire, Paul G., Das, Arup

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Epigenetics, Autism Spectrum, and Neurodevelopmental Disorders حسب Rangasamy, Sampathkumar, D’Mello, Santosh R., Narayanan, Vinodh

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A Potential Role for Angiopoietin 2 in the Regulation of the Blood–Retinal Barrier in Diabetic Retinopathy حسب Rangasamy, Sampathkumar, Srinivasan, Ramprasad, Maestas, Joann, McGuire, Paul G., Das, Arup

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Reduced neuronal size and mTOR pathway activity in the Mecp2 A140V Rett syndrome mouse model حسب Rangasamy, Sampathkumar, Olfers, Shannon, Gerald, Brittany, Hilbert, Alex, Svejda, Sean, Narayanan, Vinodh

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Do Genomic Factors Play a Role in Diabetic Retinopathy? حسب Cabrera, Andrea P., Monickaraj, Finny, Rangasamy, Sampathkumar, Hobbs, Sam, McGuire, Paul, Das, Arup

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Chemokine Mediated Monocyte Trafficking into the Retina: Role of Inflammation in Alteration of the Blood-Retinal Barrier in Diabetic Retinopathy حسب Rangasamy, Sampathkumar, McGuire, Paul G., Franco Nitta, Carolina, Monickaraj, Finny, Oruganti, Sreenivasa R., Das, Arup

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Transcriptomics Analysis of Pericytes from Retinas of Diabetic Animals reveals Novel Genes and Molecular Pathways relevant to Blood-Retinal Barrier alterations in Diabetic Retinopa... حسب Rangasamy, Sampathkumar, Monickaraj, Finny, Legendre, Christophe, Cabrera, Andrea P, Llaci, Lorida, Bilagody, Cherae, McGuire, Paul, Das, Arup

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A Common Nonsynonymous Single Nucleotide Polymorphism in the SLC30A8 Gene Determines ZnT8 Autoantibody Specificity in Type 1 Diabetes حسب Wenzlau, Janet M., Liu, Yu, Yu, Liping, Moua, Ong, Fowler, Kimberly T., Rangasamy, Sampathkumar, Walters, Jay, Eisenbarth, George S., Davidson, Howard W., Hutton, John C.

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Improved methods for RNAseq-based alternative splicing analysis حسب Halperin, Rebecca F., Hegde, Apurva, Lang, Jessica D., Raupach, Elizabeth A., Legendre, Christophe, Liang, Winnie S., LoRusso, Patricia M., Sekulic, Aleksandar, Sosman, Jeffrey A., Trent, Jeffrey M., Rangasamy, Sampathkumar, Pirrotte, Patrick, Schork, Nicholas J.

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Two additional males with X‐linked, syndromic mental retardation carry de novo mutations in HNRNPH2 حسب Jepsen, Wayne M., Ramsey, Keri, Szelinger, Szabolcs, Llaci, Lorida, Balak, Chris, Belnap, Newell, Bilagody, Cherae, De Both, Matthew, Gupta, Raj, Naymik, Marcus, Pandey, Richa, Piras, Ignazio S., Sanchez‐Castillo, Meredith, Rangasamy, Sampathkumar, Narayanan, Vinodh, Huentelman, Matthew J.

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Case Report: Novel mutations in TBC1D24 are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disabilit... حسب Banuelos, Erika, Ramsey, Keri, Belnap, Newell, Krishnan, Malavika, Balak, Chris, Szelinger, Szabolcs, Siniard, Ashley L., Russell, Megan, Richholt, Ryan, De Both, Matt, Piras, Ignazio, Naymik, Marcus, Claasen, Ana M., Rangasamy, Sampathkumar, Huentelman, Matthew J., Craig, David W., Campeau, Philippe M., Narayanan, Vinodh, Schrauwen, Isabelle

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Congenital myasthenic syndrome caused by a frameshift insertion mutation in GFPT1 حسب Szelinger, Szabolcs, Krate, Jonida, Ramsey, Keri, Strom, Samuel P., Shieh, Perry B., Lee, Hane, Belnap, Newell, Balak, Chris, Siniard, Ashley L., Russell, Megan, Richholt, Ryan, Both, Matt De, Claasen, Ana M., Schrauwen, Isabelle, Nelson, Stanley F., Huentelman, Matthew J., Craig, David W., Yang, Samuel P., Moore, Steven A., Sivakumar, Kumaraswamy, Narayanan, Vinodh, Rangasamy, Sampathkumar

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Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish حسب Siekierska, Aleksandra, Stamberger, Hannah, Deconinck, Tine, Oprescu, Stephanie N., Partoens, Michèle, Zhang, Yifan, Sourbron, Jo, Adriaenssens, Elias, Mullen, Patrick, Wiencek, Patrick, Hardies, Katia, Lee, Jeong-Soo, Giong, Hoi-Khoanh, Distelmaier, Felix, Elpeleg, Orly, Helbig, Katherine L., Hersh, Joseph, Isikay, Sedat, Jordan, Elizabeth, Karaca, Ender, Kecskes, Angela, Lupski, James R., Kovacs-Nagy, Reka, May, Patrick, Narayanan, Vinodh, Pendziwiat, Manuela, Ramsey, Keri, Rangasamy, Sampathkumar, Shinde, Deepali N., Spiegel, Ronen, Timmerman, Vincent, von Spiczak, Sarah, Helbig, Ingo, Weckhuysen, Sarah, Francklyn, Christopher, Antonellis, Anthony, de Witte, Peter, De Jonghe, Peter

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Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation حسب Balak, Chris, Benard, Marianne, Schaefer, Elise, Iqbal, Sumaiya, Ramsey, Keri, Ernoult-Lange, Michèle, Mattioli, Francesca, Llaci, Lorida, Geoffroy, Véronique, Courel, Maité, Naymik, Marcus, Bachman, Kristine K., Pfundt, Rolph, Rump, Patrick, ter Beest, Johanna, Wentzensen, Ingrid M., Monaghan, Kristin G., McWalter, Kirsty, Richholt, Ryan, Le Béchec, Antony, Jepsen, Wayne, De Both, Matt, Belnap, Newell, Boland, Anne, Piras, Ignazio S., Deleuze, Jean-François, Szelinger, Szabolcs, Dollfus, Hélène, Chelly, Jamel, Muller, Jean, Campbell, Arthur, Lal, Dennis, Rangasamy, Sampathkumar, Mandel, Jean-Louis, Narayanan, Vinodh, Huentelman, Matt, Weil, Dominique, Piton, Amélie

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