Risultati della ricerca - Deepa Selvi Rani

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  1. 1
    Y Chromosome Deletions in Azoospermic Men in India

    Y Chromosome Deletions in Azoospermic Men in India di Kumarasamy Thangaraj, Nalini Gupta, Kadupu Pavani, Alla G. Reddy, Subbaya Subramainan, Deepa Selvi Rani, Bibaswan Ghosh, Baidyanath Chakravarty, Lalji Singh

    Pubblicazione 2003
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  2. 2
    Mechanistic Heterogeneity in Contractile Properties of α-Tropomyosin (TPM1) Mutants Associated with Inherited Cardiomyopathies

    Mechanistic Heterogeneity in Contractile Properties of α-Tropomyosin (TPM1) Mutants Associated with Inherited Cardiomyopathies di Tejas M. Gupte, Farah Haque, Binnu Gangadharan, Margaret S. Sunitha, Souhrid Mukherjee, Swetha Anandhan, Deepa Selvi Rani, Namita Mukundan, Amruta Jambekar, Kumarasamy Thangaraj, Ramanathan Sowdhamini, Ruth F. Sommese, Suman Nag, James A. Spudich, John A. Mercer

    Pubblicazione 2014
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  3. 3
    A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia

    A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia di Perundurai S. Dhandapany, Sakthivel Sadayappan, Yali Xue, Gareth T. Powell, Deepa Selvi Rani, Prathiba Nallari, Taranjit Singh, Madhu Khullar, Pedro Soares, Ajay Bahl, Jagan Mohan Tharkan, Pradeep Vaideeswar, Andiappan Rathinavel, Calambur Narasimhan, Dharma Rakshak Ayapati, Qasim Ayub, S. Qasim Mehdi, Stephen Oppenheimer, Martin Richards, Alkes L. Price, Nick Patterson, David Reich, Lalji Singh, Chris Tyler‐Smith, Kumarasamy Thangaraj

    Pubblicazione 2009
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  4. 4
    Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities

    Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities di Martin W. Breuss, Julian Ik‐Tsen Heng, Karine Poirier, Guoling Tian, Xavier H. Jaglin, Zhengdong Qu, Andreas Braun, Thomas Gstrein, Linh Ngo, Matilda Haas, Nadia Bahi‐Buisson, Marie‐Laure Moutard, Sandrine Passemard, Alain Verloès, Pierre Gressèns, Yunli Xie, Kathryn Robson, Deepa Selvi Rani, Kumarasamy Thangaraj, Tim Clausen, Jamel Chelly, Nicholas J. Cowan, David A. Keays

    Pubblicazione 2012
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  5. 5
    RAF1 mutations in childhood-onset dilated cardiomyopathy

    RAF1 mutations in childhood-onset dilated cardiomyopathy di Perundurai S. Dhandapany, Abdur Razzaque, Uthiralingam Muthusami, Sreejith Kunnoth, Jonathan J. Edwards, Sonia Mulero‐Navarro, Ilan Riess, Sherly Pardo, Jipo Sheng, Deepa Selvi Rani, Bindhu Rani, Periyasamy Govindaraj, Elisabetta Flex, Tomohiro Yokota, Michiko Furutani, Tsutomu Nishizawa, Toshio Nakanishi, Jeffrey Robbins, Giuseppe Limongelli, Roger J. Hajjar, Djamel Lebeche, Ajay Bahl, Madhu Khullar, Andiappan Rathinavel, Kirsten C. Sadler, Marco Tartaglia, Rumiko Matsuoka, Kumarasamy Thangaraj, Bruce D. Gelb

    Pubblicazione 2014
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