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pro vyhledávání: '"Methilation"'
Autor:
Martins, Amanda de Abreu
A Distrofia Muscular de Duchenne (DMD) é uma doença hereditária ligada ao cromossomo ‘X’ que tem como principais características a atrofia e fraqueza muscular progressiva, chegando até mesmo ao comprometimento da musculatura cardíaca e resp
Autor:
Alberto Magi, Francesca Demichelis, Chiara Biagioni, Gian Marco Franceschini, Ilenia Migliaccio, Matteo Benelli, Dario Romagnoli, Luca Malorni
Publikováno v:
Communications Biology
Communications Biology, Vol 4, Iss 1, Pp 1-15 (2021)
Communications Biology, Vol 4, Iss 1, Pp 1-15 (2021)
Differentially DNA methylated regions (DMRs) inform on the role of epigenetic changes in cancer. We present Rocker-meth, a new computational method exploiting a heterogeneous hidden Markov model to detect DMRs across multiple experimental platforms.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f5cac28dc21696bc33c52248b528fa2
https://pubmed.ncbi.nlm.nih.gov/34728774
https://pubmed.ncbi.nlm.nih.gov/34728774
Autor:
Mihailović, Jelena M.
Publikováno v:
Универзитет у Београду
Тумори који захватају централи нервни систем, првенствено ендокранијум, представљају посебан изазов у дијагностици магнетном резонанц
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=nardusnacion::c7049bd13646ed63d4880014cee7ef3e
https://hdl.handle.net/21.15107/rcub_nardus_9361
https://hdl.handle.net/21.15107/rcub_nardus_9361
Autor:
Amanda de Abreu Martins
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
A Distrofia Muscular de Duchenne (DMD) é uma doença hereditária ligada ao cromossomo ‘X’ que tem como principais características a atrofia e fraqueza muscular progressiva, chegando até mesmo ao comprometimento da musculatura cardíaca e resp
Autor:
Silvia Alemany, Mar Fatjó-Vilas, Juan C. Leza, Lourdes Fañanás, Ana González-Pinto, Igor Nenadic, Aldo Córdova-Palomera, Ximena Goldberg
Publikováno v:
PLoS ONE
Addi. Archivo Digital para la Docencia y la Investigación
instname
Recercat. Dipósit de la Recerca de Catalunya
Dipòsit Digital de la UB
Universidad de Barcelona
PLoS ONE, Vol 9, Iss 8, p e103639 (2014)
Addi. Archivo Digital para la Docencia y la Investigación
instname
Recercat. Dipósit de la Recerca de Catalunya
Dipòsit Digital de la UB
Universidad de Barcelona
PLoS ONE, Vol 9, Iss 8, p e103639 (2014)
Neurodevelopmental disruptions caused by obstetric complications play a role in the etiology of several phenotypes associated with neuropsychiatric diseases and cognitive dysfunctions. Importantly, it has been noticed that epigenetic processes occurr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c42c4def43920c18bfbeb98e24c5e5d
https://pubmed.ncbi.nlm.nih.gov/25171170
https://pubmed.ncbi.nlm.nih.gov/25171170
Autor:
NASELLI, Flores, Modica, M, ATTANZIO, Alessandro, CARADONNA, Fabio, GENTILE, Carla, TESORIERE, Luisa, LIVREA, Maria Antonia
Phytochemicals play prominent roles in human diet and nutrition as protective redo-active substances in prevention of several disorders and chronic diseases in humans. Today, their function as potent modulators of the mammalian epigenome-regulated ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3658::a8bb108e5594d17e1aed2fd0dcb8c812
http://hdl.handle.net/10447/63848
http://hdl.handle.net/10447/63848
Autor:
Oryaşın, Erman
ermTR geni özellikle streptokoklarda makrolidlere direnç sağlayan en yaygın genlerden biridir. ermTR klonlanarak hassas suşlardaki etkisi gözlenmemiştir. Bu çalışmanın amacı izogenik durumda ermTR geninin etkisini göstermektir. Şimdiye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b18f76ba7a8f61adf772957b13dd4faf
https://acikbilim.yok.gov.tr/handle/20.500.12812/583948
https://acikbilim.yok.gov.tr/handle/20.500.12812/583948
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