Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Aramati Bindu Madhava Reddy"'
Publikováno v:
Cell Death and Disease, Vol 14, Iss 12, Pp 1-19 (2023)
Abstract The E3 ubiquitin ligase WWP1 (WW Domain-containing E3 Ubiquitin Protein Ligase 1) is a member of the HECT (Homologous to the E6-associated protein Carboxyl Terminus) E3 ligase family. It is conserved across several species and plays crucial
Externí odkaz:
https://doaj.org/article/5c7b1f454df043da80631b80b9faf407
Autor:
Meher Bolisetti Gayatri, Rama Krishna Kancha, Abhayananda Behera, Dorababu Patchva, Nagaraj Velugonda, Sadasivudu Gundeti, Aramati Bindu Madhava Reddy
Publikováno v:
Cell Death Discovery, Vol 9, Iss 1, Pp 1-12 (2023)
Abstract Imatinib resistance remains an unresolved problem in CML disease. Activation of JAK2/STAT3 pathway and increased expression of RUNX1 have become one reason for development of imatinib resistance in CML subjects. Metformin has gained attentio
Externí odkaz:
https://doaj.org/article/3d3b4f3397d24ba483df1239aecf2893
Autor:
Rao, Kandrakonda Yelamanda, Basha, Shaik Jeelan, Monika, Kallubai, Gajula, Navya Naidu, Sivakumar, Irla, Kumar, Sandeep, Vadde, Ramakrishna, Aramati, Bindu Madhava Reddy, Subramanyam, Rajagopal, Damu, Amooru Gangaiah
Publikováno v:
Journal of Biomolecular Structure & Dynamics; 2023, Vol. 41 Issue 20, p11148-11165, 18p
Autor:
Yelamanda Rao, Kandrakonda, Jeelan Basha, Shaik, Monika, Kallubai, Naidu Gajula, Navya, Sivakumar, Irla, Kumar, Sandeep, Vadde, Ramakrishna, Aramati, Bindu Madhava Reddy, Subramanyam, Rajagopal, Damu, Amooru Gangaiah
Publikováno v:
Journal of Biomolecular Structure and Dynamics; December 2023, Vol. 41 Issue: 20 p11148-11165, 18p
Autor:
Sarfraz Ahmad, Afroz Alam, Saeed Ali, Sekani Allen, Dinakara Rao Ampasala, Santosh Anand, Vinit Singh Baghel, Obul Reddy Bandapalli, Ankit Banik, Serena Bao, Riyaz Basha, Lambodar Behera, Santosh Kumar Behera, L.V.K.S. Bhaskar, Shivaleela Biradar, Pallaval Veera Bramhachari, Amajala Krishna Chaitanya, Nyshadham S.N. Chaitanya, Anandita Chakraborty, Gayathri Chalikonda, Ambika Chamoli, Gorantla Sri Charitha, Aejaz Ahmad Dar, Vineeta Dixit, Ravindra Donde, Victoria Dulemba, Bala Prabhakar Girish, Gayatri Gouda, Manoj Kumar Gupta, Areeba Hafeez, Nwamaka Iloani, Sri Krishna Jayadev Magani, Kiran Kalia, Pavan Kumar Kancharla, Anupama Sindhghatta Kariyappa, K.M. Kiran Kumar, Narayanan Krishnaswamy, Neeraj Kulkarni, Binayak Kumar, Babu R. Lamani, Christoffer Lambring, Dhatri Madduru, Kishore Madhamanchi, Pradeep Madhamanchi, Rama Rao Malla, Amit Mandoli, Hariharasudan Mani, Sravanthi Mannem, Rakshmitha Marni, Arundhati Mehta, Neha Merchant, Mathavan Muthaiyan, Prakash Nadoor, Ganji Purnachandra Nagaraju, Rashmi Nagesh, M. Naveen Kumar, Prakash Babu Panithi, Pranathi Pappu, Rajeshwari H. Patil, Dahrii Paul, Sujatha Peela, Murugavel Ponnusamy, Gudivad Indu Priya, Senthilkumar Rajagopal, Sowbhagya Ramachandregowda, Panchareddy Madhava Rao, Fayyaz Rasool, Aramati Bindu Madhava Reddy, Bichismita Sahu, Tarun Sahu, Umesh T. Sankpal, Deepu Sharma, Karishma Shaw, Sapnita Shinde, Suchita Dattatray Shinde, Dhananjay Shukla, Vigneshwar Suriya Prakash Sinnarasan, Ngalah Bidii Stephen, Prashanth Suravajhala, Ravikiran Tekupalli, Atul Kumar Tiwari, Soumitra Tiwari, Ramakrishna Vadde, Amouda Venkatesan, Henu Kumar Verma, Urvashi Vijay, Naveen Kumar Vishvakarma, Muralidhar Yegireddy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b926ff77c6efc01e96ddf58176089aa
https://doi.org/10.1016/b978-0-323-98807-0.00029-6
https://doi.org/10.1016/b978-0-323-98807-0.00029-6
Akademický článek
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Autor:
Aramati Bindu Madhava, Reddy, Kiranpreet, Kaur, Anil Kumar, Mandal, Shirly George, Panicker, Ravi, Thomas, Seyed Ehtesham, Hasnain, Dorairajan, Balasubramanian, Subhabrata, Chakrabarti
Publikováno v:
Molecular vision. 10
The human Cytochrome P450 gene CYP1B1 has been implicated in primary congenital glaucoma worldwide. The aim of this study was to understand the role of CYP1B1 mutations in causing primary congenital glaucoma in Indian populations.The study included 6
Autor:
Sreelatha, Komatireddy, Subhabrata, Chakrabarti, Anil Kumar, Mandal, Aramati Bindu Madhava, Reddy, Srirangan, Sampath, Shirly George, Panicker, Dorairajan, Balasubramanian
Publikováno v:
Molecular vision. 9
Axenfeld-Rieger anomaly (ARA) is a form of anterior segment dysgenesis of the eye, mainly caused by mutations in the FOXC1 gene. We had earlier reported a novel mutation in the wing region of FOXC1 in an autosomal dominant family. The present study w