Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Suparna Mukhopadhyay"'
Autor:
Tapan Kumar Ray, Ashutosh Arora, Ashok Kumar Dargar, Chandra Mohan Arora, Suparna Mukhopadhyay, Pulak M. Pandey
Publikováno v:
Springer Proceedings in Energy ISBN: 9789811045752
This paper is discussing development of Hard Anodized Aluminium Oxide (HAAO) coated Solar Receivers with varying degree of surface roughness and finishing of HAAO coatings for comparative analysis. It is found that for lower DNI, roughness Ra 150 μm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f88d449b89ba78c7731359fd59affa32
https://doi.org/10.1007/978-981-10-4576-9_12
https://doi.org/10.1007/978-981-10-4576-9_12
Publikováno v:
Cancer Letters. 241:13-22
Mutations in DNA are generally considered to have an etiologic role in the development of cancer. If so, it follows that reducing the frequency of such mutations will reduce the incidence of cancer induced by mutagens. Recent advances in elucidating
Autor:
Elangovan Krishnan, Suparna Mukhopadhyay, W. Glenn McGregor, Bodduluri Haribabu, Chad A. Dumstorf
Publikováno v:
Molecular cancer research : MCR. 7(2)
The somatic mutation hypothesis of cancer predicts that reducing the frequency of mutations induced by carcinogens will reduce the incidence of cancer. To examine this, we developed an antimutator strategy based on the manipulation of the level of a
Publikováno v:
Nucleic Acids Research
Comparative mutagenesis of 1,N(6)-ethenoadenine (epsilonA) and 8-oxoguanine (8-oxoG), two endogenous DNA lesions that are also formed by exogenous DNA damaging agents, have been evaluated in HeLa and xeroderma pigmentosum variant (XPV) cell extracts.
Autor:
Nicholas B. Watson, Wolfgang Zacharias, Denise R. Clark, W. Glenn McGregor, Suparna Mukhopadhyay
Publikováno v:
Nucleic acids research. 32(19)
The REV1 gene encodes a Y-family DNA polymerase that has been postulated to have both catalytic and structural functions in translesion replication past UV photoproducts in mammalian cells. To examine if REV1 is implicated in DNA damage tolerance mec
Autor:
Neal S. Peachey, Maureen A. McCall, Suparna Mukhopadhyay, Machelle T. Pardue, Sherry L. Ball, Sophie I. Candille, Ronald G. Gregg
Publikováno v:
Investigative ophthalmologyvisual science. 44(1)
PURPOSE. The available evidence indicates that the naturally occurring mouse mutant nob (no b-wave) provides an animal model for the complete form of human X-linked congenital stationary night blindness (CSNB1). The goals of the present study were to
Publikováno v:
Molecular Therapy. 13:S374
Top of pageAbstract Recent advances in understanding the molecular mechanisms of carcinogen-induced mutagenesis indicate that most mutations are dependent on the activity of newly-described translesion DNA polymerases, which have reduced base-pairing