Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Pretto, Dalyir"'
Autor:
Sun, Yao-Hui, Kao, Hillary K.J., Thai, Phung N., Smithers, Regan, Chang, Che-Wei, Pretto, Dalyir, Yechikov, Sergey, Oppenheimer, Sarah, Bedolla, Amanda, Chalker, Brooke A., Ghobashy, Rana, Nolta, Jan A., Chan, James W., Chiamvimonvat, Nipavan, Lieu, Deborah K.
Publikováno v:
In Cell Reports 26 December 2023 42(12)
Autor:
Yechikov, Sergey, Kao, Hillary K.J., Chang, Che-Wei, Pretto, Dalyir, Zhang, Xiao-Dong, Sun, Yao-Hui, Smithers, Regan, Sirish, Padmini, Nolta, Jan A., Chan, James W., Chiamvimonvat, Nipavan, Lieu, Deborah K.
Publikováno v:
In Stem Cell Research December 2020 49
Autor:
AlOlaby, Reem Rafik, Sweha, Stefan R., Silva, Marisol, Durbin-Johnson, Blythe, Yrigollen, Carolyn M., Pretto, Dalyir, Hagerman, Randi J., Tassone, Flora
Publikováno v:
In Brain and Development June 2017 39(6):483-492
Autor:
Pretto, Dalyir I., Kumar, Madhur, Cao, Zhengyu, Cunningham, Christopher L., Durbin-Johnson, Blythe, Qi, Lihong, Berman, Robert, Noctor, Stephen C., Hagerman, Randi J., Pessah, Isaac N., Tassone, Flora
Publikováno v:
In Neurobiology of Aging May 2014 35(5):1189-1197
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Pretto, Dalyir I, Eid, John S, Yrigollen, Carolyn M, Tang, Hiu-Tung, Loomis, Erick W, Raske, Chris, Durbin-Johnson, Blythe, Hagerman, Paul J, Tassone, Flora
Publikováno v:
Journal of medical genetics, vol 52, iss 1
BackgroundOver 40% of male and ∼16% of female carriers of a premutation FMR1 allele (55-200 CGG repeats) will develop fragile X-associated tremor/ataxia syndrome, an adult onset neurodegenerative disorder, while about 20% of female carriers will de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::15734032d0358a92051221e79a869737
https://escholarship.org/uc/item/1z81k101
https://escholarship.org/uc/item/1z81k101
Autor:
Periasamy, Ammasi, So, Peter T. C., König, Karsten, Chang, Che-Wei, Kao, Hillary K. J., Sun, Yao-Hui, Pretto, Dalyir I., Lieu, Deborah K., Chan, James W.
Publikováno v:
Proceedings of SPIE; February 2020, Vol. 11244 Issue: 1 p112442H-112442H-9, 1011988p
Autor:
Sun, Yao‐Hui, Kao, Hillary K.J., Chang, Che‐Wei, Merleev, Alexander, Overton, James L., Pretto, Dalyir, Yechikov, Sergey, Maverakis, Emanual, Chiamvimonvat, Nipavan, Chan, James W., Lieu, Deborah K.
Publikováno v:
Stem Cells; January 2020, Vol. 38 Issue: 1 p90-101, 12p
Autor:
Pretto, Dalyir I, Mendoza-Morales, Guadalupe, Lo, Joyce, Cao, Ru, Hadd, Andrew, Latham, Gary J, Durbin-Johnson, Blythe, Hagerman, Randi, Tassone, Flora
Publikováno v:
Journal of medical genetics, vol 51, iss 5
BackgroundGreater than 200 CGG repeats in the 5'UTR of the FMR1 gene lead to epigenetic silencing and lack of the FMR1 protein, causing fragile X Syndrome. Individual carriers of a premutation (PM) allele with 55-200 CGG repeats are typically unmethy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::5957f5a655723aa060e2e62d7b05661e
https://escholarship.org/uc/item/0120s4cg
https://escholarship.org/uc/item/0120s4cg
Autor:
Pretto, Dalyir I., Kumar, Madhur, Cao, Zhengyu, Cunningham, Christopher L., Durbin-Johnson, Blythe, Qi, Lihong, Berman, Robert, Noctor, Stephen C., Hagerman, Randi J., Pessah, Isaac N., Tassone, Flora
A premutation (PM) expansion (55-200 CGG) in the fragile X mental retardation gene 1 causes elevated messenger RNA and reduced fragile X mental retardation gene 1 protein. Young PM carriers can develop characteristic physical features and mild cognit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df5bbee6b4184409cabba1594c9fd464
https://europepmc.org/articles/PMC4062976/
https://europepmc.org/articles/PMC4062976/