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

by Kumar, Sivakumar Prasanth, Parmar, Vilas R., Jasrai, Yogesh T., Pandya, Himanshu A.
Published in J Chem Biol (2015)

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

by Patel, Chirag N., Kumar, Sivakumar Prasanth, Pandya, Himanshu A., Rawal, Rakesh M.
Published in Mol Divers (2020)

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

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

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

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

A multiparametric organ toxicity predictor for drug discovery

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

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

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

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

by 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
Published in Brain (2017)

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

by 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
Published in Nat Genet (2019)

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

by 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
Published in Nat Genet (2019)

Neuronal intranuclear inclusion disease is genetically heterogeneous

by 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
Published in Ann Clin Transl Neurol (2020)

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

by 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
Published in EMBO J (2018)

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

by 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
Published in J Clin Invest (2020)