Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Sanjiban Chakrabarty"'
Autor:
Shreyas Hulusemane Karunakara, Sangavi Eswaran, Sandeep Mallya, Padmanaban S. Suresh, Sanjiban Chakrabarty, Shama Prasada Kabekkodu
Publikováno v:
BMC Research Notes, Vol 17, Iss 1, Pp 1-11 (2024)
Abstract Objective miR-497/195, located at 17p13.1, is a highly conserved miRNA cluster whose abnormal expression is a key regulator of carcinogenesis. We performed a comprehensive analysis of the miR-497/195 cluster to determine its prognostic utili
Externí odkaz:
https://doaj.org/article/e0cf0db1b3a0445a8d93baf981d442c4
Autor:
Sriharikrishnaa Srinath, Padacherri Vethil Jishnu, Vinay Koshy Varghese, Vaibhav Shukla, Divya Adiga, Sandeep Mallya, Sanjiban Chakrabarty, Krishna Sharan, Deeksha Pandey, Aniruddha Chatterjee, Shama Prasada Kabekkodu
Publikováno v:
Molecular Oncology, Vol 18, Iss 6, Pp 1608-1630 (2024)
Cervical cancer (CC) is a key contributor to cancer‐related mortality in several countries. The identification of molecular markers and the underlying mechanism may help improve CC management. We studied the regulation and biological function of th
Externí odkaz:
https://doaj.org/article/cf41f896dd704757979fc5ce69d93704
Autor:
Amoolya Kandettu, Divya Adiga, Vasudha Devi, Padmanaban S. Suresh, Sanjiban Chakrabarty, Raghu Radhakrishnan, Shama Prasada Kabekkodu
Publikováno v:
Genes and Diseases, Vol 9, Iss 6, Pp 1443-1465 (2022)
Ovarian cancer (OC) is one of the most common and fatal types of gynecological cancer. OC is usually detected at the advanced stages of the disease, making it highly lethal. miRNAs are single-stranded, small non-coding RNAs with an approximate size r
Externí odkaz:
https://doaj.org/article/005fe28ecef84386b30e3b861c349b34
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2023)
Externí odkaz:
https://doaj.org/article/409715e2636d409f807daa6ab27b7bba
Autor:
Kanaka Sai Ram Padam, Richard Morgan, Keith Hunter, Sanjiban Chakrabarty, Naveena A. N. Kumar, Raghu Radhakrishnan
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract The role of evolutionarily conserved homeobox-containing HOX genes as transcriptional regulators in the developmental specification of organisms is well known. The contribution of HOX genes involvement in oral cancer phenotype has yet to be
Externí odkaz:
https://doaj.org/article/365347a3e8104a2d8be713bbf5028de8
Autor:
Raviprasad Kuthethur, Divya Adiga, Amoolya Kandettu, Maria Sona Jerome, Sandeep Mallya, Kamalesh Dattaram Mumbrekar, Shama Prasada Kabekkodu, Sanjiban Chakrabarty
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2023)
Introduction: Forkhead (FOX) transcription factors are involved in cell cycle control, cellular differentiation, maintenance of tissues, and aging. Mutation or aberrant expression of FOX proteins is associated with developmental disorders and cancers
Externí odkaz:
https://doaj.org/article/d5869414ceee40499dcc648cdc960e56
Publikováno v:
Pharmacological Research, Vol 180, Iss , Pp 106239- (2022)
DOC2B is a ubiquitously expressed isoform of the double C-2 protein family that requires Ca2+ for most of its physiological functions. Initial findings have indicated that DOC2B participates in exocytosis, vesicular transport, insulin secretion and r
Externí odkaz:
https://doaj.org/article/46c1f744c1d7403997761cefe6470ccd
Autor:
Samatha Bhat, Shama Prasada Kabekkodu, Vinay Koshy Varghese, Sanjiban Chakrabarty, Sandeep P Mallya, Harish Rotti, Deeksha Pandey, Pralhad Kushtagi, Kapaettu Satyamoorthy
Publikováno v:
Tumor Biology, Vol 39 (2017)
Multicomponent molecular modifications such as DNA methylation may offer sensitive and specific cervical intraepithelial neoplasia and cervical cancer biomarkers. In this study, we tested cervical tissues at various stages of tumor progression for 5-
Externí odkaz:
https://doaj.org/article/7affb66d9e33410c9331920aad1b1c00
Autor:
Divya Adiga, Samatha Bhat, Vaibhav Shukla, Henil Vinit Shah, Raviprasad Kuthethur, Sanjiban Chakrabarty, Shama Prasada Kabekkodu
Publikováno v:
Free Radical Biology and Medicine. 201:1-13
Publikováno v:
Biochimie. 207:122-136
Ribosomopathies are rare congenital disorders associated with defective ribosome biogenesis due to pathogenic variations in genes that encode proteins related to ribosome function and biogenesis. Defects in ribosome biogenesis result in a nucleolar s