Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Aryaman J"'
Autor:
Aryaman J. Singh, Siddharth Wala, Saiyadali H. Ladakhan, Rakshith B. Sreesha, Somashekara M Adinarayanappa
Publikováno v:
Materials Today: Proceedings.
Autor:
Jai Aditya Jhamb, Sanjiv Rampal, Ashish Jaiman, Ajantha Sinniah, Jia Bei Tong, Aryaman Jaiman
Publikováno v:
Ķazaķstannyṇ Klinikalyķ Medicinasy, Vol 20, Iss 5, Pp 4-8 (2023)
Air pollution is widely recognized as a future biohazard, yet its direct effects on human health, particularly in relation to bone health and vitamin D levels, are inadequately understood. While the detrimental impact on respiratory and cardiovascula
Externí odkaz:
https://doaj.org/article/50c0eb1433014ef4ae82a0a687514f91
Autor:
Aryaman Joshi, Shweata Maurya, Atharva Mahale, Soumya Lipsa Rath, Timir Tripathi, Aditya K. Padhi
Publikováno v:
ACS Omega, Vol 8, Iss 41, Pp 37852-37863 (2023)
Externí odkaz:
https://doaj.org/article/405ab2f14fc545cd9fccb274d006d663
Autor:
Wei, W, Keogh, MJ, Aryaman, J, Golder, Z, Kullar, PJ, Wilson, I, Talbot, K, Turner, MR, McKenzie, C-A, Troakes, C, Attems, J, Smith, C, Sarraj, SA, Morris, CM, Ansorge, O, Jones, NS, Ironside, JW, Chinnery, PF
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics
Wei, W, Keogh, M J, Aryaman, J, Golder, Z, Kullar, P J, Wilson, I, Talbot, K, Turner, M R, McKenzie, C-A, Troakes, C, Attems, J, Smith, C, Sarraj, S A, Morris, C M, Ansorge, O, Jones, N S, Ironside, J W & Chinnery, P F 2018, ' Frequency and signature of somatic variants in 1461 human brain exomes ', Genetics in Medicine . https://doi.org/10.1038/s41436-018-0274-3
Wei, W, Keogh, M J, Aryaman, J, Golder, Z, Kullar, P J, Wilson, I, Talbot, K, Turner, M R, McKenzie, C-A, Troakes, C, Attems, J, Smith, C, Sarraj, S A, Morris, C M, Ansorge, O, Jones, N S, Ironside, J W & Chinnery, P F 2018, ' Frequency and signature of somatic variants in 1461 human brain exomes ', Genetics in Medicine . https://doi.org/10.1038/s41436-018-0274-3
Purpose To systematically study somatic variants arising during development in the human brain across a spectrum of neurodegenerative disorders. Methods In this study we developed a pipeline to identify somatic variants from exome sequencing data in
Cell-to-cell heterogeneity drives a range of (patho)physiologically important phenomena, such as cell fate and chemotherapeutic resistance. The role of metabolism, and particularly of mitochondria, is increasingly being recognized as an important exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6260bde5dd61991398bbb5ec3c445ece
http://arxiv.org/abs/1809.01878
http://arxiv.org/abs/1809.01878
Autor:
Keogh, M, Wei, W, Aryaman, J, Wilson, I, Talbot, K, Turner, M, McKenzie, C, Troakes, C, Attems, J, Smith, C, Al Sarraj, S, Morris, C, Ansorge, O, Pickering-Brown, S, Jones, N, Ironside, J, Chinnery, P
Publikováno v:
Keogh, M J, Wei, W, Aryaman, J, Wilson, I, Talbot, K, Turner, M R, McKenzie, C-A, Troakes, C, Attems, J, Smith, C, Al-Sarraj, S, Morris, C M, Ansorge, O, Pickering-Brown, S, Jones, N, Ironside, J W & Chinnery, P F 2018, ' Oligogenic genetic variation of neurodegenerative disease genes in 980 postmortem human brains ', Journal of Neurology, Neurosurgery & Psychiatry . https://doi.org/10.1136/jnnp-2017-317234
Journal of Neurology, Neurosurgery, and Psychiatry
Keogh, M J, Wei, W, Aryaman, J, Wilson, I, Talbot, K, Turner, M R, Mckenzie, C, Troakes, C, Attems, J, Smith, C, Al Sarraj, S, Morris, C M, Ansorge, O, Pickering-brown, S, Jones, N, Ironside, J W & Chinnery, P F 2018, ' Oligogenic genetic variation of neurodegenerative disease genes in 980 postmortem human brains ', Journal of Neurology, Neurosurgery & Psychiatry, vol. 89, no. 8, pp. 813-816 . https://doi.org/10.1136/jnnp-2017-317234
Journal of Neurology, Neurosurgery, and Psychiatry
Keogh, M J, Wei, W, Aryaman, J, Wilson, I, Talbot, K, Turner, M R, Mckenzie, C, Troakes, C, Attems, J, Smith, C, Al Sarraj, S, Morris, C M, Ansorge, O, Pickering-brown, S, Jones, N, Ironside, J W & Chinnery, P F 2018, ' Oligogenic genetic variation of neurodegenerative disease genes in 980 postmortem human brains ', Journal of Neurology, Neurosurgery & Psychiatry, vol. 89, no. 8, pp. 813-816 . https://doi.org/10.1136/jnnp-2017-317234
Background Several studies suggest that multiple rare genetic variants in genes causing monogenic forms of neurodegenerative disorders interact synergistically to increase disease risk or reduce the age of onset, but these studies have not been valid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d38c99b145c49fc032a9e297e88f82eb
https://www.repository.cam.ac.uk/handle/1810/273241
https://www.repository.cam.ac.uk/handle/1810/273241
Mitochondrial dysfunction is involved in a wide array of devastating diseases, but the heterogeneity and complexity of the symptoms of these diseases challenges theoretical understanding of their causation. With the explosion of omics data, we have t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1032::d65b3a768310a2f1e2a010f96f6dc1a6
http://hdl.handle.net/10044/1/52595
http://hdl.handle.net/10044/1/52595
Heterogeneity in mitochondrial content has been previously suggested as a major contributor to cellular noise, with multiple studies indicating its direct involvement in biomedically important cellular phenomena. A recently published dataset explored
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1032::ebd88d011ad34a0a67689d4f416ed11c
http://hdl.handle.net/10044/1/48451
http://hdl.handle.net/10044/1/48451
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.