Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Krishna Kumar Rathnam"'
Autor:
Lalatendu Moharana, Soumya Surath Panda, Suma Devaraj, Ghanashyam Biswas, Ganesh Chandra Subudhi, Prasant Kumar Parida, Sourav Kumar Mishra, Jogamaya Pattnaik, Sambit Mohanty, Sukanya Karunanidhi, Sandhya Lakshmi Singuluri, S. V. Saju, Krishna Kumar Rathnam, Amit Sehrawat, Shikha Mudgal, Sunu Lazar Cyriac, Ashwin Philips, Anil Kumar Jose, Prasant Ganesan
Publikováno v:
South Asian Journal of Cancer, Vol 13, Iss 02, Pp 114-120 (2024)
Externí odkaz:
https://doaj.org/article/590a79baadb248298cd247cb3963a8fe
Autor:
Raja Thirumalairaj, Purvish M. Parikh, Amit Agarwal, Randeep Singh, Arvind Krishnamurthy, Sharad S. Desai, Amita Maheshwari, Prashant Mehta, Abdul Ghafur, S. P. Somashekhar, Ahamed Iqbal, Dhairyasheel N. Savant, Syed Md Akram Hussain, Amit Bhatt, Tashi Wangdi, Jyoti Bajpai, Anantbhushan A. Ranade, K. Govind Babu, Ajay Bapna, Ghanshyam Biswas, Hemant Malhotra, M. Vamshi Krishna, Rajendra Prasad Baral, Rajesh Vashishtha, Ahmad Javid Safi, Sharmila Agarwal, J. P. Agarwal, Krishna Kumar Rathnam, P. N. Mohapatra, Rajeev Vijay Kumar, Senthil Rajappa, Sewanti Atul Limaye, Amish Vora, Vijay A.P. Reddy, Bhavesh B. Parekh, G. K. Rath
Publikováno v:
South Asian Journal of Cancer, Vol 10, Iss 01, Pp 03-08 (2021)
We provide the South Asian Declaration, containing the consensus guidelines for coronavirus disease 2019 (COVID-19) vaccination in cancer patients.
Externí odkaz:
https://doaj.org/article/e4c4ceebd616401184eba80b615aacea
Autor:
Taruna Rajagopal, Arun Seshachalam, Krishna Kumar Rathnam, Srikanth Talluri, Sivaramakrishnan Venkatabalasubramanian, Nageswara Rao Dunna
Publikováno v:
PLoS ONE, Vol 17, Iss 1 (2022)
Background Homologous recombination repair (HRR) accurately repairs the DNA double-strand breaks (DSBs) and is crucial for genome stability. Genetic polymorphisms in crucial HRR pathway genes might affect genome stability and promote tumorigenesis. U
Externí odkaz:
https://doaj.org/article/dc1e492abef94ed5a095856a78bd7160
Publikováno v:
Oman Journal of Ophthalmology, Vol 2, Iss 2, Pp 102-103 (2009)
Externí odkaz:
https://doaj.org/article/a34378afcdd940978e6dccea0dfc76ba
Autor:
Arvind Krishnamurthy, R. P. Baral, Amish Vora, Hemant Malhotra, Krishna Kumar Rathnam, Sharad S. Desai, Raja Thirumalairaj, Randeep Singh, Tashi Wangdi, Purvish M. Parikh, Bhavesh B. Parekh, Sharmila Agarwal, Ajay Bapna, G. K. Rath, Abdul Ghafur, Ahamed Iqbal, Dhairyasheel Savant, Sewanti Limaye, Rajesh Vashishtha, Jyoti Bajpai, Amita Maheshwari, Rajeev Vijay Kumar, G. Biswas, Senthil Rajappa, Vijay Anand Reddy, Ahmad Javid Safi, Prashant Mehta, Syed Md Akram Hussain, K. Govind Babu, Jolly Agarwal, Amit Bhatt, Anantbhushan Ranade, Amit Agarwal, P. N. Mohapatra, S.P. Somashekhar, M. Vamshi Krishna
Publikováno v:
South Asian Journal of Cancer
South Asian Journal of Cancer, Vol 10, Iss 01, Pp 03-08 (2021)
South Asian Journal of Cancer, Vol 10, Iss 01, Pp 03-08 (2021)
We provide the South Asian Declaration, containing the consensus guidelines for coronavirus disease 2019 (COVID-19) vaccination in cancer patients.
Autor:
Arun Seshachalam, Nageswara Rao Dunna, Taruna Rajagopal, Swarna Viswanathan, Arunachalam Jothi, Krishna Kumar Rathnam, Srikanth Talluri
Publikováno v:
Molecular Biology Reports. 47:5081-5090
Identification of modifier genes predisposing to breast cancer (BC) phenotype remains a significant challenge and varies with ethnicity. The genetic variability observed in DNA repair genes may modulate the cell's ability to repair the damaged DNA an
Autor:
Arun Seshachalam, Taruna Rajagopal, Krishna Kumar Rathnam, Nageswara Rao Dunna, Sivaramakrishnan Venkatabalasubramanian, Arunachalam Jothi, Srikanth Talluri
Publikováno v:
Molecular biology reports. 49(4)
The frequency of triple-negative breast cancer (TNBC) incidence varies among different populations, suggesting the involvement of genetic component towards TNBC development. Previous studies have reported that BRCA1/2 germline mutations confer a life
Autor:
Nageswara Rao Dunna, Arunachalam Jothi, Srikanth Talluri, Krishna Kumar Rathnam, Arun Seshachalam, R.L. Akshaya, Taruna Rajagopal
Publikováno v:
Gene. 762
Until now, no study has reported the combined effect of genetic variants of HOTAIR and NME1 towards breast cancer (BC) pathogenesis. Hence, the aim of the present study is to determine the risk of breast cancer development with HOTAIR (rs920778 C T a
Publikováno v:
International Journal of Research in Medical Sciences. 9:236
Background: Cancer is a leading cause of death worldwide, accounting for 8.2 million deaths in 2012. Febrile neutropenia (FN) is fever associated with abnormally low neutrophil count signifying an immunocompromised state secondary to malignancy or it
Autor:
Franck E. Nicolini, Jayasree Sreenivasan, Michael J. Mauro, Hugues de Lavallade, Andrew Whiteley, Mudgal Kothekar, Krishna Kumar Rathnam, Gregor Verhoef, Alessandro Lucchesi, Tapan Saikia, Michael W. Deininger, Aude Charbonnier, Navin Khattry, Geetanjali Chimote, Bimba Hv, Jane F. Apperley, Carlo Gambacorti-Passerini, Jorge E. Cortes, Granacher Nikki, Siu-Long Yao, Dong-Wook Kim, Shashikant Apte
Publikováno v:
Blood. 134:4158-4158
Introduction: Despite availability of several BCR-ABL1 TKIs for treatment of CML, some patients (pts) fail ≥3 TKIs and/or have co-morbidities that limit use of 2nd generation TKIs (2GTKI: Nilotinib, Dasatinib and Ponatinib). K0706 is a novel third