Prediction of protein targets of kinetin using in silico and in vitro methods: a case study on spinach seed germination mechanism

gan Kumar, Sivakumar Prasanth, Parmar, Vilas R., Jasrai, Yogesh T., Pandya, Himanshu A.
Cyhoeddwyd yn J Chem Biol (2015)

Identification of potential inhibitors of coronavirus hemagglutinin-esterase using molecular docking, molecular dynamics simulation and binding free energy calculation

gan Patel, Chirag N., Kumar, Sivakumar Prasanth, Pandya, Himanshu A., Rawal, Rakesh M.
Cyhoeddwyd yn Mol Divers (2020)

Evolutionary and Molecular Aspects of Indian Tomato Leaf Curl Virus Coat Protein

gan Kumar, Sivakumar Prasanth, Patel, Saumya K., Kapopara, Ravi G., Jasrai, Yogesh T., Pandya, Himanshu A.
Cyhoeddwyd 2012

Development of cardiotoxicity model using ligand-centric and receptor-centric descriptors

gan Chirag N Patel, Sivakumar Prasanth Kumar, Rakesh M Rawal, Manishkumar B Thaker, Himanshu A Pandya
Cyhoeddwyd 2020-11-01

A multiparametric organ toxicity predictor for drug discovery

gan Patel, Chirag N., Kumar, Sivakumar Prasanth, Rawal, Rakesh M., Patel, Daxesh P., Gonzalez, Frank J., Pandya, Himanshu A.
Cyhoeddwyd yn Toxicol Mech Methods (2019)

Epitope-Based Immunoinformatics and Molecular Docking Studies of Nucleocapsid Protein and Ovarian Tumor Domain of Crimean–Congo Hemorrhagic Fever Virus

gan Srinivasan, Pappu, Kumar, Sivakumar Prasanth, Karthikeyan, Muthusamy, Jeyakanthan, Jeyaram, Jasrai, Yogesh T., Pandya, Himanshu A., Rawal, Rakesh M., Patel, Saumya K.
Cyhoeddwyd 2011

Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in ‘FUSDelta14’ knockin mice

gan Devoy, Anny, Kalmar, Bernadett, Stewart, Michelle, Park, Heesoon, Burke, Beverley, Noy, Suzanna J, Redhead, Yushi, Humphrey, Jack, Lo, Kitty, Jaeger, Julian, Mejia Maza, Alan, Sivakumar, Prasanth, Bertolin, Cinzia, Soraru, Gianni, Plagnol, Vincent, Greensmith, Linda, Acevedo Arozena, Abraham, Isaacs, Adrian M, Davies, Benjamin, Fratta, Pietro, Fisher, Elizabeth M C
Cyhoeddwyd yn Brain (2017)

Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia

gan Cortese, Andrea, Simone, Roberto, Sullivan, Roisin, Vandrovcova, Jana, Tariq, Huma, Yau, Wai Yan, Humphrey, Jack, Jaunmuktane, Zane, Sivakumar, Prasanth, Polke, James, Ilyas, Muhammad, Tribollet, Eloise, Tomaselli, Pedro J., Devigili, Grazia, Callegari, Ilaria, Versino, Maurizio, Salpietro, Vincenzo, Efthymiou, Stephanie, Kaski, Diego, Wood, Nick W., Andrade, Nadja S., Buglo, Elena, Rebelo, Adriana, Rossor, Alexander M., Bronstein, Adolfo, Fratta, Pietro, Marques, Wilson J., Züchner, Stephan, Reilly, Mary M., Houlden, Henry
Cyhoeddwyd yn Nat Genet (2019)

Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia

gan Cortese, Andrea, Simone, Roberto, Sullivan, Roisin, Vandrovcova, Jana, Tariq, Huma, Yau, Wai Yan, Humphrey, Jack, Jaunmuktane, Zane, Sivakumar, Prasanth, Polke, James, llyas, Muhammad, Tribollet, Eloise, Tomaselli, Pedro J., Devigili, Grazia, Callegari, Ilaria, Versino, Maurizio, Salpietro, Vincenzo, Efthymiou, Stephanie, Kaski, Diego, Wood, Nick W., Andrade, Nadja S., Buglo, Elena, Rebelo, Adriana, Rossor, Alexander M., Bronstein, Adolfo, Fratta, Pietro, Marques, Wilson J., Züchner, Stephan, Reilly, Mary M., Houlden, Henry
Cyhoeddwyd yn Nat Genet (2019)

Neuronal intranuclear inclusion disease is genetically heterogeneous

gan Chen, Zhongbo, Yan Yau, Wai, Jaunmuktane, Zane, Tucci, Arianna, Sivakumar, Prasanth, Gagliano Taliun, Sarah A., Turner, Chris, Efthymiou, Stephanie, Ibáñez, Kristina, Sullivan, Roisin, Bibi, Farah, Athanasiou‐Fragkouli, Alkyoni, Bourinaris, Thomas, Zhang, David, Revesz, Tamas, Lashley, Tammaryn, DeTure, Michael, Dickson, Dennis W., Josephs, Keith A., Gelpi, Ellen, Kovacs, Gabor G., Halliday, Glenda, Rowe, Dominic B., Blair, Ian, Tienari, Pentti J., Suomalainen, Anu, Fox, Nick C., Wood, Nicholas W., Lees, Andrew J., Haltia, Matti J., Hardy, John, Ryten, Mina, Vandrovcova, Jana, Houlden, Henry
Cyhoeddwyd yn Ann Clin Transl Neurol (2020)

Mice with endogenous TDP‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis

gan Fratta, Pietro, Sivakumar, Prasanth, Humphrey, Jack, Lo, Kitty, Ricketts, Thomas, Oliveira, Hugo, Brito‐Armas, Jose M, Kalmar, Bernadett, Ule, Agnieszka, Yu, Yichao, Birsa, Nicol, Bodo, Cristian, Collins, Toby, Conicella, Alexander E, Mejia Maza, Alan, Marrero‐Gagliardi, Alessandro, Stewart, Michelle, Mianne, Joffrey, Corrochano, Silvia, Emmett, Warren, Codner, Gemma, Groves, Michael, Fukumura, Ryutaro, Gondo, Yoichi, Lythgoe, Mark, Pauws, Erwin, Peskett, Emma, Stanier, Philip, Teboul, Lydia, Hallegger, Martina, Calvo, Andrea, Chiò, Adriano, Isaacs, Adrian M, Fawzi, Nicolas L, Wang, Eric, Housman, David E, Baralle, Francisco, Greensmith, Linda, Buratti, Emanuele, Plagnol, Vincent, Fisher, Elizabeth MC, Acevedo‐Arozena, Abraham
Cyhoeddwyd yn EMBO J (2018)

Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia

gan Prudencio, Mercedes, Humphrey, Jack, Pickles, Sarah, Brown, Anna-Leigh, Hill, Sarah E., Kachergus, Jennifer M., Shi, J., Heckman, Michael G., Spiegel, Matthew R., Cook, Casey, Song, Yuping, Yue, Mei, Daughrity, Lillian M., Carlomagno, Yari, Jansen-West, Karen, de Castro, Cristhoper Fernandez, DeTure, Michael, Koga, Shunsuke, Wang, Ying-Chih, Sivakumar, Prasanth, Bodo, Cristian, Candalija, Ana, Talbot, Kevin, Selvaraj, Bhuvaneish T., Burr, Karen, Chandran, Siddharthan, Newcombe, Jia, Lashley, Tammaryn, Hubbard, Isabel, Catalano, Demetra, Kim, Duyang, Propp, Nadia, Fennessey, Samantha, Fagegaltier, Delphine, Phatnani, Hemali, Secrier, Maria, Fisher, Elizabeth M.C., Oskarsson, Björn, van Blitterswijk, Marka, Rademakers, Rosa, Graff-Radford, Neil R., Boeve, Bradley F., Knopman, David S., Petersen, Ronald C., Josephs, Keith A., Thompson, E. Aubrey, Raj, Towfique, Ward, Michael, Dickson, Dennis W., Gendron, Tania F., Fratta, Pietro, Petrucelli, Leonard
Cyhoeddwyd yn J Clin Invest (2020)