Hasil Pencarian - Moulinath Acharya
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P142: Whole-exome analyses of non-syndromic hearing loss patients from India reveal a wide spectrum of known and novel mutations* oleh Sudipta Chakraborty, Sukanya Mitra, Shamita Sanga, Arnab Ghosh, Suchandra Mukherjee, Nidhan Biswas, Moulinath Acharya
Diterbitkan 2023-01-01
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Amyloid beta precursor protein and prion protein have a conserved interaction affecting cell adhesion and CNS development. oleh Darcy M Kaiser, Moulinath Acharya, Patricia L A Leighton, Hao Wang, Nathalie Daude, Serene Wohlgemuth, Beipei Shi, W Ted Allison
Diterbitkan 2012-01-01
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NOTCH pathway inactivation reprograms stem-like oral cancer cells to JAK-STAT dependent state and provides the opportunity of synthetic lethality oleh Subhashis Ghosh, Paromita Mitra, Uday Saha, Rimpa Nandi, Subhashree Jena, Arnab Ghosh, Shantanu Saha Roy, Moulinath Acharya, Nidhan Kumar Biswas, Sandeep Singh
Diterbitkan 2023-06-01
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Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy oleh Shamita Sanga, Sudipta Chakraborty, Mainak Bardhan, Kiran Polavarapu, Veeramani Preethish Kumar, Chandrika Bhattacharya, Saraswati Nashi, Seena Vengalil, Thenral S. Geetha, Vedam Ramprasad, Atchayaram Nalini, Analabha Basu, Moulinath Acharya
Diterbitkan 2023-09-01
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