Search Results - Horvath, Shanti

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  1. 1
    Salicylates are interference compounds in TR-FRET assays

    Salicylates are interference compounds in TR-FRET assays by Hanley, Ronan P., Horvath, Shanti, An, Jianghong, Hof, Fraser, Wulff, Jeremy E.

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  2. 2
    Selective Inhibition of CBX6: A Methyllysine Reader Protein in the Polycomb Family

    Selective Inhibition of CBX6: A Methyllysine Reader Protein in the Polycomb Family by Milosevich, Natalia, Gignac, Michael C, McFarlane, James, Simhadri, Chakravarthi, Horvath, Shanti, Daze, Kevin D, Croft, Caitlin S, Dheri, Aman, Quon, Taylor T. H, Douglas, Sarah F, Wulff, Jeremy E, Paci, Irina, Hof, Fraser

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  3. 3
    Biallelic PTPMT1 variants disrupt cardiolipin metabolism and lead to a neurodevelopmental syndrome

    Biallelic PTPMT1 variants disrupt cardiolipin metabolism and lead to a neurodevelopmental syndrome by Falabella, Micol, Pizzamiglio, Chiara, Tabara, Luis Carlos, Munro, Benjamin, Abdel-Hamid, Mohamed S, Sonmezler, Ece, Macken, William L, Lu, Shanti, Tilokani, Lisa, Flannery, Padraig J, Patel, Nina, Pope, Simon A S, Heales, Simon J R, Hammadi, Dania B H, Alston, Charlotte L, Taylor, Robert W, Lochmuller, Hanns, Woodward, Cathy E, Labrum, Robyn, Vandrovcova, Jana, Houlden, Henry, Chronopoulou, Efstathia, Pierre, Germaine, Maroofian, Reza, Hanna, Michael G, Taanman, Jan-Willem, Hiz, Semra, Oktay, Yavuz, Zaki, Maha S, Horvath, Rita, Prudent, Julien, Pitceathly, Robert D S

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  4. 4
    Mutant PTPMT1 disrupts cardiolipin metabolism and mitochondrial bioenergetics leading to a neurodevelopmental syndrome

    Mutant PTPMT1 disrupts cardiolipin metabolism and mitochondrial bioenergetics leading to a neurodevelopmental syndrome by Falabella, Micol, Pizzamiglio, Chiara, Tabara, Luis Carlos, Munro, Benjamin, Abdel-Hamid, Mohamed S., Sonmezler, Ece, Macken, William L., Lu, Shanti, Tilokani, Lisa, Flannery, Padraig J., Pope, Simon A.S., Heales, Simon J.R., Hammadi, Dania B.H., Alston, Charlotte L., Taylor, Robert W., Lochmuller, Hanns, Chronopoulou, Efstathia, Pierre, Germaine, Maroofian, Reza, Hanna, Michael G., Taanman, Jan-Willem, Hiz, Semra, Oktay, Yavuz, Zaki, Maha S., Horvath, Rita, Prudent, Julien, Pitceathly, Robert D.S.

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  5. 5
    Biochemical signatures mimicking multiple carboxylase deficiency in children with mutations in MT-ATP6

    Biochemical signatures mimicking multiple carboxylase deficiency in children with mutations in MT-ATP6 by Larson, Austin A, Balasubramaniam, Shanti, Christodoulou, John, Burrage, Lindsay C, Marom, Ronit, Graham, Brett H, Diaz, George A, Glamuzina, Emma, Hauser, Natalie, Heese, Bryce, Horvath, Gabriella, Mattman, Andre, van Karnebeek, Clara, Lane Rutledge, S, Williamson, Amy, Estrella, Lissette, Van Hove, Johan K L, Weisfeld-Adams, James D

    Published in Mitochondrion
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