Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Apurva Puvar"'
Autor:
Jayna Raghwani, Louis du Plessis, John T. McCrone, Sarah C. Hill, Kris V. Parag, Julien Thézé, Dinesh Kumar, Apurva Puvar, Ramesh Pandit, Oliver G. Pybus, Guillaume Fournié, Madhvi Joshi, Chaitanya Joshi
Publikováno v:
Emerging Infectious Diseases, Vol 28, Iss 4, Pp 751-758 (2022)
Limited genomic sampling in many high-incidence countries has impeded studies of severe respiratory syndrome coronavirus 2 (SARS-CoV-2) genomic epidemiology. Consequently, critical questions remain about the generation and global distribution of viru
Externí odkaz:
https://doaj.org/article/dda72a171cde471ab0bda7baf89135e7
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 13, Iss 4, Pp GD01-GD02 (2019)
Limb Girdle Muscular Dystrophy-Type 2A (LGMD-2A) is an autosomal recessive disease caused due to mutation in the Calpain-3 (CAPN3) gene, leading to partial or total loss of protein. In India, LGMD-2A is the most prevalence form of the disease account
Externí odkaz:
https://doaj.org/article/30c69ee5840c41619f588de93a40a634
Autor:
Purva Gohil, Kajal Patel, Kishan Purohit, Dhruvil Chavda, Apurva Puvar, Vishal S. Suthar, Deepak B. Patil, Madhavi Joshi, Chaitanya G. Joshi
Publikováno v:
Tropical Animal Health and Production. 54
The present study, using 16 s rRNA sequencing of the V3-V4 hypervariable region, was aimed to check diversity of vaginal microbiota throughout different stages of the estrous cycle in Bos indicus, with attention to changes in progesterone hormone and
Autor:
Ramesh J. Pandit, Chaitanya Joshi, Guillaume Fournie, Louis du Plessis, Sarah C. Hill, Madhvi Joshi, Kris V Parag, John T. McCrone, Apurva Puvar, Oliver G. Pybus, Julien Thézé, Jayna Raghwani, Dinesh Kumar
Genomic surveillance of SARS-CoV-2 has played a decisive role in understanding the transmission and evolution of the virus during its emergence and continued circulation. However, limited genomic sampling in many high-incidence countries has impeded
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7837d8ede9c492808af1e8eb07ab5671
https://doi.org/10.1101/2021.08.31.21262680
https://doi.org/10.1101/2021.08.31.21262680
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 13, Iss 4, Pp GD01-GD02 (2019)
Limb Girdle Muscular Dystrophy-Type 2A (LGMD-2A) is an autosomal recessive disease caused due to mutation in the Calpain-3 (CAPN3) gene, leading to partial or total loss of protein. In India, LGMD-2A is the most prevalence form of the disease account