Zobrazeno 1 - 10
of 4 784
pro vyhledávání: '"S. BANERJI"'
Autor:
Anthony Baptista, Alessandro Barp, Tapabrata Chakraborti, Chris Harbron, Ben D. MacArthur, Christopher R. S. Banerji
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract Deep neural networks (DNNs) are powerful tools for approximating the distribution of complex data. It is known that data passing through a trained DNN classifier undergoes a series of geometric and topological simplifications. While some pro
Externí odkaz:
https://doaj.org/article/97e8c4f8b80743829e934cc3478f8c28
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-14 (2024)
Abstract Complex biological processes, such as cellular differentiation, require intricate rewiring of intra-cellular signalling networks. Previous characterisations revealed a raised network entropy underlies less differentiated and malignant cell s
Externí odkaz:
https://doaj.org/article/e0128e2e8e774f77a26841625fa62c15
Autor:
Prasenjit Das, D. Padmalal, K.P.N. Kumaran, Ruta B. Limaye, S. Vishnu Mohan, Upasana S. Banerji, Ravi Bhushan
Publikováno v:
Quaternary Science Advances, Vol 14, Iss , Pp 100197- (2024)
The Central Kerala coast in Southwest India serves as a valuable natural archive for studies of the Late Quaternary coastal evolution, palaeoclimate, and maritime trades. The coast is an archeologically and culturally significant region in South Indi
Externí odkaz:
https://doaj.org/article/c851a722afb345efa7bd8c7c196b30e9
Autor:
Thuy-Hang Nguyen, Lise Paprzycki, Alexandre Legrand, Anne-Emilie Declèves, Philipp Heher, Maelle Limpens, Alexandra Belayew, Christopher R. S. Banerji, Peter S. Zammit, Alexandra Tassin
Publikováno v:
Skeletal Muscle, Vol 13, Iss 1, Pp 1-14 (2023)
Abstract Background Hypoxia is known to modify skeletal muscle biological functions and muscle regeneration. However, the mechanisms underlying the effects of hypoxia on human myoblast differentiation remain unclear. The hypoxic response pathway is o
Externí odkaz:
https://doaj.org/article/54f7e8b9df5a4c7f8986eef5f8194eb0
Publikováno v:
Lithosphere, Vol 2022, Iss Special 8 (2022)
AbstractDetrital zircons are frequently used for crustal evolutionary studies as they sample vast regions of the continental crust. In the present study, we utilise newly compiled U-Pb detrital zircon data from the Indian subcontinent as well as a co
Externí odkaz:
https://doaj.org/article/dfb33a8cc45d4832a93d6dba1a9a61f9
Publikováno v:
EMBO Molecular Medicine, Vol 13, Iss 8, Pp 1-25 (2021)
Abstract Facioscapulohumeral muscular dystrophy (FSHD) is characterised by progressive skeletal muscle weakness and wasting. FSHD is linked to epigenetic derepression of the subtelomeric D4Z4 macrosatellite at chromosome 4q35. Epigenetic derepression
Externí odkaz:
https://doaj.org/article/c5e23813bf1949a6b6aa84f1244f2a2a
Publikováno v:
Journal of Asian Earth Sciences: X, Vol 7, Iss , Pp 100091- (2022)
Reliable estimation of ages and temporal correlations through the Quaternary Period (
Externí odkaz:
https://doaj.org/article/27c9ec049c0b4a7b819c0232126475da
Autor:
Jithu Shaji, Upasana S. Banerji, K. Maya, Kumar Batuk Joshi, Ankur J. Dabhi, Nisha Bharti, Ravi Bhushan, D. Padmalal
Publikováno v:
Quaternary International. 642:48-62
Autor:
Christopher R. S. Banerji, Maryna Panamarova, Husam Hebaishi, Robert B. White, Frédéric Relaix, Simone Severini, Peter S. Zammit
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-13 (2017)
Facioscapulohumeral muscular dystrophy is a myopathy linked to ectopic expression of the DUX4 transcription factor. The authors show that the suppression of targets genes of the myogenesis regulator PAX7 is a signature of FSHD, and might explain oxid
Externí odkaz:
https://doaj.org/article/e4c41a2342de44989834fb0cef7eaaf9
Autor:
Christopher R. S. Banerji, Philipp Heher, John Hogan, Natalie Katz, Husain Bin Haidar, Michael D. Keegan, Colin Cernik, Rabi Tawil, Ketan Patel, Peter S. Zammit, Jeffery M. Statland
Facioscapulohumeral muscular dystrophy (FSHD) is an incurable skeletal myopathy. In absence of therapy, lifestyle factors impacting disease progression are important for clinical management. Monozygotic twins with FSHD often exhibit dramatically diff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6142fef6b8d2c2da9529c82b2413ba2c
https://doi.org/10.1101/2023.05.17.23290091
https://doi.org/10.1101/2023.05.17.23290091