Works matching AU Gupta, Vandana

Results: 196
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    NEW SOFT GENERALIZED ISOMETRIES WITH SOFT POINTS.

    Published in:
    Journal of Ramanujan Society of Mathematics & Mathematical Sciences, 2024, v. 11, n. 2, p. 117, doi. 10.56827/JRSMMS.2024.1102.8
    By:
    • Kumawat, Sandeep;
    • Gupta, Vandana;
    • Srivastava, Anjali
    Publication type:
    Article
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    Dynamic regulation of inter-organelle communication by ubiquitylation controls skeletal muscle development and disease onset.

    Published in:
    eLife, 2023, p. 1, doi. 10.7554/eLife.81966
    By:
    • Mansur, Arian;
    • Joseph, Remi;
    • Kim, Euri S.;
    • Jean-Beltran, Pierre M.;
    • Udeshi, Namrata D.;
    • Pearce, Cadence;
    • Hanjie Jiang;
    • Iwase, Reina;
    • Milev, Miroslav P.;
    • Almousa, Hashem A.;
    • McNamara, Elyshia;
    • Widrick, Jeffrey;
    • Perez, Claudio;
    • Ravenscroft, Gianina;
    • Sacher, Michael;
    • Cole, Philip A.;
    • Carr, Steven A.;
    • Gupta, Vandana A.
    Publication type:
    Article
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    Determining minimal clinically important differences in the North Star Ambulatory Assessment (NSAA) for patients with Duchenne muscular dystrophy.

    Published in:
    PLoS ONE, 2023, v. 18, n. 4, p. 1, doi. 10.1371/journal.pone.0283669
    By:
    • Ayyar Gupta, Vandana;
    • Pitchforth, Jacqueline M.;
    • Domingos, Joana;
    • Ridout, Deborah;
    • Iodice, Mario;
    • Rye, Catherine;
    • Chesshyre, Mary;
    • Wolfe, Amy;
    • Selby, Victoria;
    • Mayhew, Anna;
    • Mazzone, Elena S.;
    • Ricotti, Valeria;
    • Hogrel, Jean-Yves;
    • Niks, Erik H.;
    • de Groot, Imelda;
    • Servais, Laurent;
    • Straub, Volker;
    • Mercuri, Eugenio;
    • Manzur, Adnan Y.;
    • Muntoni, Francesco
    Publication type:
    Article
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    Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians.

    Published in:
    2020
    By:
    • Pellerin, David;
    • Aykanat, Asli;
    • Ellezam, Benjamin;
    • Troiano, Emily C.;
    • Karamchandani, Jason;
    • Dicaire, Marie‐Josée;
    • Petitclerc, Marc;
    • Robertson, Rebecca;
    • Allard‐Chamard, Xavier;
    • Brunet, Denis;
    • Konersman, Chamindra G.;
    • Mathieu, Jean;
    • Warman Chardon, Jodi;
    • Gupta, Vandana A.;
    • Beggs, Alan H.;
    • Brais, Bernard;
    • Chrestian, Nicolas;
    • Dicaire, Marie-Josée;
    • Allard-Chamard, Xavier
    Publication type:
    journal article
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    Mutation-specific effects on thin filament length in thin filament myopathy.

    Published in:
    2016
    By:
    • Winter, Josine M. de;
    • Joureau, Barbara;
    • Lee, Eun‐Jeong;
    • Kiss, Balázs;
    • Yuen, Michaela;
    • Gupta, Vandana A.;
    • Pappas, Christopher T.;
    • Gregorio, Carol C.;
    • Stienen, Ger J. M.;
    • Edvardson, Simon;
    • Wallgren‐Pettersson, Carina;
    • Lehtokari, Vilma‐Lotta;
    • Pelin, Katarina;
    • Malfatti, Edoardo;
    • Romero, Norma B.;
    • Engelen, Baziel G. van;
    • Voermans, Nicol C.;
    • Donkervoort, Sandra;
    • Bönnemann, C. G.;
    • Clarke, Nigel F.
    Publication type:
    journal article
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    Studies on phenothiazines. Part 16.

    Published in:
    Journal of Heterocyclic Chemistry, 1992, v. 29, n. 7, p. 1703, doi. 10.1002/jhet.5570290705
    By:
    • Gupta, R. R.;
    • Saraswat, Vandana;
    • Gupta, Archana;
    • Jain, Mukesh;
    • Gupta, Vandana
    Publication type:
    Article
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    ACTN2 mutations cause "Multiple structured Core Disease" (MsCD).

    Published in:
    Acta Neuropathologica, 2019, v. 137, n. 3, p. 501, doi. 10.1007/s00401-019-01963-8
    By:
    • Lornage, Xavière;
    • Romero, Norma B.;
    • Grosgogeat, Claire A.;
    • Malfatti, Edoardo;
    • Donkervoort, Sandra;
    • Marchetti, Michael M.;
    • Neuhaus, Sarah B.;
    • Foley, A. Reghan;
    • Labasse, Clémence;
    • Schneider, Raphaël;
    • Carlier, Robert Y.;
    • Chao, Katherine R.;
    • Medne, Livija;
    • Deleuze, Jean-François;
    • Orlikowski, David;
    • Bönnemann, Carsten G.;
    • Gupta, Vandana A.;
    • Fardeau, Michel;
    • Böhm, Johann;
    • Laporte, Jocelyn
    Publication type:
    Article
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    Polymorphisms in the MLL breakpoint cluster region (BCR).

    Published in:
    Human Genetics, 2003, v. 113, n. 1, p. 80, doi. 10.1007/s00439-003-0936-2
    By:
    • Echlin-Bell, Deborah R.;
    • Smith, Lydia L.;
    • Li, Loretta;
    • Strissel, Pamela L.;
    • Strick, Reiner;
    • Gupta, Vandana;
    • Banerjee, Jhula;
    • Larson, Richard;
    • Relling, Mary V.;
    • Raimondi, Susan C.;
    • Hayashi, Yasuhide;
    • Taki, Tomohiko;
    • Zeleznik-Le, Nancy;
    • Rowley, Janet D.
    Publication type:
    Article
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    Gram Shiksha Pragati Abhiyan.

    Published in:
    CURIE Journal, 2009, v. 2, n. 2, p. 67
    By:
    • Gupta, Vandana;
    • Gupta, Naveen;
    • Kumar, Manmeet
    Publication type:
    Article