Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Bithia, R"'
Autor:
Datta, Ankur a, 1, George, Neethu a, Koppolu, Tejaswini a, Kumar. S, Udhaya a, b, 2, Bithia, R. a, 3, Zayed, Hatem c, 4, Doss. C, George Priya a, ⁎, 5
Publikováno v:
In Computational Biology and Chemistry October 2024 112
Autor:
Thirumal Kumar, D. a, Udhaya Kumar, S. a, Nishaat Laeeque, Ahmed Shaikh a, Apurva Abhay, Shivalkar a, Bithia, R. a, Magesh, R. b, Kumar, Maignana c, Zayed, Hatem d, ∗, George Priya Doss, C. a, ∗
Publikováno v:
In Advances in Protein Chemistry and Structural Biology 2020 120:379-408
Autor:
Thirumal Kumar, D. a, Shaikh, Nishaat b, Bithia, R. c, Karthick, V. d, George Priya Doss, C. c, *, Magesh, R. e
Publikováno v:
In Advances in Protein Chemistry and Structural Biology 2023 135:57-96
Publikováno v:
Journal of Biomolecular Structure and Dynamics. 40:1571-1585
K-Ras is a small GTPase and acts as a molecular switch by recruiting GEFs and GAPs, and alternates between the inert GDP-bound and the dynamic GTP-bound forms. The amino acid at position 12 of K-Ras is a hot spot for oncogenic mutations (G12A, G12C,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::510ad9f88dd458899643cab4cfea9aa6
https://doi.org/10.1080/07391102.2020.1830177
https://doi.org/10.1080/07391102.2020.1830177
Autor:
Udhaya Kumar, S. a, Kamaraj, Balu b, Varghese, Rinku Polachirakkal a, Preethi, V. Anu c, Bithia, R. a, George Priya Doss, C. a, ⁎
Publikováno v:
In Advances in Protein Chemistry and Structural Biology 2022 130:351-373
Autor:
Srivarshini Sankar, C. George Priya Doss, Bithia R, R. Magesh, D. Thirumal Kumar, S. Udhaya Kumar, Hatem Zayed, Mariem Sidenna
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 11 (2020)
Frontiers in Genetics, Vol 11 (2020)
Background and Aims: Familial hypercholesterolemia (FH) is one of the major risk factor for the progression of atherosclerosis and coronary artery disease. This study focused on identifying the dysregulated molecular pathways and core genes that are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b484b29e2253df859b944f68e8718bdc
http://europepmc.org/articles/PMC7373787
http://europepmc.org/articles/PMC7373787
Autor:
Thirumal Kumar, D, Udhaya Kumar, S, Nishaat Laeeque, Ahmed Shaikh, Apurva Abhay, Shivalkar, Bithia, R, Magesh, R., Kumar, Maignana, Zayed, Hatem, George Priya Doss, C
Blau syndrome (BS), which affects the eyes, skin, and joints, is an autosomal dominant genetic inflammatory disorder. BS is caused by mutations in the NOD2 gene. However, there are no direct treatments, and treatment with conventional anti-inflammato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1664::0361dd38652a5245a04119ec2f2ff768
https://hdl.handle.net/10576/13473
https://hdl.handle.net/10576/13473
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Shivalkar Apurva Abhay, S. Udhaya Kumar, D Thirumal Kumar, Ahmed Shaikh Nishaat Laeeque, Maignana Kumar, Hatem Zayed, Bithia R, R. Magesh, C. George Priya Doss
Publikováno v:
Advances in Protein Chemistry and Structural Biology ISBN: 9780128213223
Blau syndrome (BS), which affects the eyes, skin, and joints, is an autosomal dominant genetic inflammatory disorder. BS is caused by mutations in the NOD2 gene. However, there are no direct treatments, and treatment with conventional anti-inflammato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a68c2acb27d9d4bfa344c7a1bc1845c
https://doi.org/10.1016/bs.apcsb.2019.11.005
https://doi.org/10.1016/bs.apcsb.2019.11.005