Zobrazeno 1 - 10
of 338
pro vyhledávání: '"Vinod, Scaria"'
Autor:
Pragya Gupta, Sangam Giri Goswami, Geeta Kumari, Vinodh Saravanakumar, Nupur Bhargava, Akhila Balakrishna Rai, Praveen Singh, Rahul C. Bhoyar, V. R. Arvinden, Padma Gunda, Suman Jain, Vanya Kadla Narayana, Sayali C. Deolankar, T. S. Keshava Prasad, Vivek T. Natarajan, Vinod Scaria, Shailja Singh, Sivaprakash Ramalingam
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-18 (2024)
Abstract Ex vivo cellular system that accurately replicates sickle cell disease and β-thalassemia characteristics is a highly sought-after goal in the field of erythroid biology. In this study, we present the generation of erythroid progenitor lines
Externí odkaz:
https://doaj.org/article/057cee76498e45b68c0e7b95f3a332c8
Autor:
Shahzad Mirza, V. R. Arvinden, Mercy Rophina, Jitendra Bhawalkar, Uzair Khan, Bhavin Chothani, Shivankur Singh, Tanya Sharma, Aryan Dwivedi, Ellora Pandey, Shivam Garg, Sahjid Sadrudin Mukhida, Zeeshan Shabbir Ahmed Sange, Shalini Bhaumik, Jessin Varughese, Vishwamohini Yallappa Devkar, Jyoti Singh, AnjuMol V. K., Veena K., Husen Shabbir Husen Mandviwala, Vinod Scaria, Aayush Gupta
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract Numerous speculations have continually emerged, trying to explore the association between COVID-19 infection and a varied range of demographic and clinical factors. Frontline healthcare workers have been the primary group exposed to this inf
Externí odkaz:
https://doaj.org/article/b8f6ba4503434cb6bf9331964de2e6bc
Autor:
Anura V Kurpad, Disha Sharma, KM Venkat Narayan, Ambily Sivadas, Arpita Mukhopadhyay, Greg Gibson, Abhinav Jain, S Sahana, Bani Jolly, Rahul C Bhoyar, Mohamed Imran, Vigneshwar Senthivel, Mohit Kumar Divakar, Anushree Mishra, Sridhar Sivasubbu, Vinod Scaria
Publikováno v:
BMJ Open Diabetes Research & Care, Vol 12, Iss 2 (2024)
Introduction Genetic variants contribute to differential responses to non-insulin antidiabetic drugs (NIADs), and consequently to variable plasma glucose control. Optimal control of plasma glucose is paramount to minimizing type 2 diabetes-related lo
Externí odkaz:
https://doaj.org/article/5f63fe82d3b64dc390f49848b985ce41
Autor:
Ramcharan Singh Angom, Adita Joshi, Ashok Patowary, Ambily Sivadas, Soundhar Ramasamy, Shamsudheen K. V., Kriti Kaushik, Ankit Sabharwal, Mukesh Kumar Lalwani, Subburaj K., Naresh Singh, Vinod Scaria, Sridhar Sivasubbu
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 12 (2024)
LncRNA-based control affects cardiac pathophysiologies like myocardial infarction, coronary artery disease, hypertrophy, and myotonic muscular dystrophy. This study used a gene-break transposon (GBT) to screen zebrafish (Danio rerio) for insertional
Externí odkaz:
https://doaj.org/article/e5967b2e3f234059a3f2916dd3a79a73
Publikováno v:
PLoS ONE, Vol 19, Iss 5, p e0303787 (2024)
BackgroundAdvances in Next Generation Sequencing have made rapid variant discovery and detection widely accessible. To facilitate a better understanding of the nature of these variants, American College of Medical Genetics and Genomics and the Associ
Externí odkaz:
https://doaj.org/article/9eae5062c8ea46b4ae40bee5cc582de0
Autor:
Pragya Gupta, V. R. Arvinden, Priya Thakur, Rahul C. Bhoyar, Vinodh Saravanakumar, Narendra Varma Gottumukkala, Sangam Giri Goswami, Mehwish Nafiz, Aditya Ramdas Iyer, Harie Vignesh, Rajat Soni, Nupur Bhargava, Padma Gunda, Suman Jain, Vivek Gupta, Sridhar Sivasubbu, Vinod Scaria, Sivaprakash Ramalingam
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2023)
β-hemoglobinopathies such as β-thalassemia (BT) and Sickle cell disease (SCD) are inherited monogenic blood disorders with significant global burden. Hence, early and affordable diagnosis can alleviate morbidity and reduce mortality given the lack
Externí odkaz:
https://doaj.org/article/a6cb5d12882b4757acc144143da96ca8
Autor:
Arti Saini, Rahul Mewara, Bhawna Verma, Inder Singh, Vinod Scaria, Binukumar Bk, Neerja Gupta, Divya Radhakrishnan, A Elavarasi, Anu Gupta, Vishnu Vy, Mamta Singh, Rohit Bhatia, Achal Srivastava, Mv Srivastava, Roopa Rajan
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S930- (2023)
Externí odkaz:
https://doaj.org/article/b656b6afbc4645939a9d9302d3cb73b7
Autor:
Savino Sciascia, Dario Roccatello, Marco Salvatore, Claudio Carta, Laura L. Cellai, Gianluca Ferrari, Aimè Lumaka, Stephen Groft, Yasemin Alanay, Maleeha Azam, Gareth Baynam, Helene Cederroth, Eva Maria Cutiongco-de la Paz, Vajira Harshadeva Weerabaddana Dissanayake, Roberto Giugliani, Claudia Gonzaga-Jauregui, Dineshani Hettiarachchi, Oleg Kvlividze, Guida Landoure, Prince Makay, Béla Melegh, Ugur Ozbek, Ratna Dua Puri, Vanessa I. Romero, Vinod Scaria, Saumya S. Jamuar, Vorasuk Shotelersuk, William A. Gahl, Samuel A. Wiafe, Olaf Bodamer, Manuel Posada, Domenica Taruscio
Publikováno v:
Frontiers in Public Health, Vol 11 (2023)
BackgroundPatients, families, the healthcare system, and society as a whole are all significantly impacted by rare diseases (RDs). According to various classifications, there are currently up to 9,000 different rare diseases that have been recognized
Externí odkaz:
https://doaj.org/article/da71af76c6954864ad49d713a5a8c259
Autor:
K. Varsha Mohan, Alaknanda Mishra, Abaranjitha Muniyasamy, Prakriti Sinha, Parul Sahu, Ashwani Kesarwani, Kshama Jain, Perumal Nagarajan, Vinod Scaria, Manisha Agarwal, Naseem S. Akhter, Chanda Gupta, Pramod Upadhyay
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background Retinitis pigmentosa (RP) is a hereditary retinal disease which leads to visual impairment. The onset and progression of RP has physiological consequences that affects the ocular environment. Some of the key non-genetic factors wh
Externí odkaz:
https://doaj.org/article/f434b379cc6343818acff51001d5c769
Autor:
Anjali Bajaj, Vigneshwar Senthivel, Rahul Bhoyar, Abhinav Jain, Mohamed Imran, Mercy Rophina, Mohit Kumar Divakar, Bani Jolly, Ankit Verma, Anushree Mishra, Disha Sharma, Siddharthan Deepti, Gautam Sharma, Raghav Bansal, Rakesh Yadav, Vinod Scaria, Nitish Naik, Sridhar Sivasubbu
Publikováno v:
Human Genomics, Vol 16, Iss 1, Pp 1-15 (2022)
Abstract Background The prevalence and genetic spectrum of cardiac channelopathies exhibit population-specific differences. We aimed to understand the spectrum of cardiac channelopathy-associated variations in India, which is characterised by a genet
Externí odkaz:
https://doaj.org/article/52afe3dfd7c645cf9500eb6a4849bb92