Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Aditya Venkatesh"'
Autor:
Kian Huat Lim, Zhou Han, Hyun Yong Jeon, Jacob Kach, Enxuan Jing, Sebastien Weyn-Vanhentenryck, Mikaela Downs, Anna Corrionero, Raymond Oh, Juergen Scharner, Aditya Venkatesh, Sophina Ji, Gene Liau, Barry Ticho, Huw Nash, Isabel Aznarez
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-13 (2020)
Restoration of normal gene expression is one way to treat monogenic disorders. Here the authors target naturally occurring non-productive alternative splicing using antisense oligonucleotides to promote the production of functional proteins.
Externí odkaz:
https://doaj.org/article/b4b17242c1b24dc9905cc03dd97077f2
Autor:
Jenny Xie, Min Peng, Shawna Guillemette, Steven Quan, Stephanie Maniatis, Yuliang Wu, Aditya Venkatesh, Scott A Shaffer, Robert M Brosh, Sharon B Cantor
Publikováno v:
PLoS Genetics, Vol 8, Iss 7, p e1002786 (2012)
BRCA1 promotes DNA repair through interactions with multiple proteins, including CtIP and FANCJ (also known as BRIP1/BACH1). While CtIP facilitates DNA end resection when de-acetylated, the function of FANCJ in repair processing is less well defined.
Externí odkaz:
https://doaj.org/article/55403aa009d0482db1dff30292132bf5
Autor:
Huw M. Nash, Barry Ticho, Juergen Scharner, Mikaela Downs, Hyun Yong Jeon, Sebastien M. Weyn-Vanhentenryck, Sophina Ji, Anna Corrionero, Isabel Aznarez, Enxuan Jing, Kian-Huat Lim, Jacob Kach, Aditya Venkatesh, Zhou Han, Raymond S Oh, Gene Liau
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-13 (2020)
Nature Communications
Nature Communications
While most monogenic diseases are caused by loss or reduction of protein function, the need for technologies that can selectively increase levels of protein in native tissues remains. Here we demonstrate that antisense-mediated modulation of pre-mRNA
Autor:
K. A. Sumithra Devi, Gagan Deep Shivamadhu, Aditya Venkatesh, Aishwarya Alva, Daniya Nausheer
Publikováno v:
International Journal of Recent Technology and Applied Science. 2:66-74
PortaX Secure Automation System Using IoT – A Survey In recent times, everything around us is automated. People are looking to make things easier and easier day by day, by reducing the work they do, but not reduce the efficiency of work. The most i
Publikováno v:
Emerging Technologies in Data Mining and Information Security ISBN: 9789811597732
There has been a shift in protest dynamics in the 2019 Hong Kong protests, when compared to the Hong Kong Umbrella Protests of 2014. The intensity, magnitude and characteristics of the movement in 2019 were perceptibly different. This work presents a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa84e61b2c4e893483e1e217d65ce205
https://doi.org/10.1007/978-981-15-9774-9_10
https://doi.org/10.1007/978-981-15-9774-9_10
Publikováno v:
International Journal of Aviation, Aeronautics, and Aerospace.
Autor:
Aditya Venkatesh, Aishwarya Alva, Daniya Nausheer, Gagan Deep Shivamadhu, K. A. Sumithra Devi
Publikováno v:
Lecture Notes in Networks and Systems ISBN: 9789811573446
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f534fec1b6d673d3d6dafa15cdd30a33
https://doi.org/10.1007/978-981-15-7345-3_81
https://doi.org/10.1007/978-981-15-7345-3_81
Publikováno v:
Molecular Vision
Purpose The apoptotic mechanisms responsible for secondary cone death in retinitis pigmentosa (RP) remain largely unknown. The cone-enriched apoptotic protease caspase-7 (Casp7) is thought to be triggered by endoplasmic reticulum (ER) stress and play
Autor:
Marybeth Baumgartner, Claudio Punzo, Ion I. Mandoiu, Aditya Venkatesh, Sahar Al Seesi, Rahul N. Kanadia, Ashley M Kilcollins, Sean Congdon, Abdul Rouf Banday, Christopher Lemoine, Devi Krishna Priya Karunakaran
Publikováno v:
Cell Cycle. 13:2526-2541
In the mammalian genome, each histone family contains multiple replication-dependent paralogs, which are found in clusters where their transcription is thought to be coupled to the cell cycle. Here, we wanted to interrogate the transcriptional regula
Retinitis pigmentosa (RP) is an inherited photoreceptor degenerative disorder that results in blindness. The disease is often caused by mutations in genes that are specific to rod photoreceptors; however, blindness results from the secondary loss of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0f87441a3bc43a1d3d18fcc7a872157