Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Minh Q. Bui"'
Autor:
David E. Godler, Yoshimi Inaba, Minh Q. Bui, David Francis, Cindy Skinner, Charles E. Schwartz, David J. Amor
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 13, p 10712 (2023)
This study characterizes the DNA methylation patterns specific to fragile X syndrome (FXS) with a full mutation (FM > 200 CGGs), premutation (PM 55–199 CGGs), and X inactivation in blood and brain tissues at the 3′ boundary of the FMR1 promoter.
Externí odkaz:
https://doaj.org/article/00af5fd39945494a8a0dae15bc2b553d
Autor:
Danuta Z. Loesch, Bruce E. Kemp, Minh Q. Bui, Paul R. Fisher, Claire Y. Allan, Oana Sanislav, Kevin R. W. Ngoei, Anna Atkinson, Flora Tassone, Sarah J. Annesley, Elsdon Storey
Publikováno v:
Frontiers in Psychiatry, Vol 12 (2021)
Fragile X Associated Tremor/Ataxia Syndrome (FXTAS) is a neurodegenerative disorder affecting carriers of premutation alleles (PM) of the X-linked FMR1 gene, which contain CGG repeat expansions of 55–200 range in a non-coding region. This late-onse
Externí odkaz:
https://doaj.org/article/ae4074102c024825816d2c1abaa6b6b0
Autor:
Sarah J. Annesley, Sui T. Lay, Shawn W. De Piazza, Oana Sanislav, Eleanor Hammersley, Claire Y. Allan, Lisa M. Francione, Minh Q. Bui, Zhi-Ping Chen, Kevin R. W. Ngoei, Flora Tassone, Bruce E. Kemp, Elsdon Storey, Andrew Evans, Danuta Z. Loesch, Paul R. Fisher
Publikováno v:
Disease Models & Mechanisms, Vol 9, Iss 11, Pp 1295-1305 (2016)
In combination with studies of post-mortem Parkinson's disease (PD) brains, pharmacological and genetic models of PD have suggested that two fundamental interacting cellular processes are impaired – proteostasis and mitochondrial respiration. We ha
Externí odkaz:
https://doaj.org/article/96d199417b6546faba92ecd66b2679dc
Autor:
Darren R. Hocking, Danuta Z. Loesch, Nicholas Trost, Minh Q. Bui, Eleanor Hammersley, David Francis, Flora Tassone, Elsdon Storey
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
This study explores the relationships between hemispheric and cerebellar white matter lesions and motor and cognitive impairments in male carriers of Fragile-X Mental Retardation 1 (FMR1) premutation alleles, and in a subgroup of these carriers affec
Externí odkaz:
https://doaj.org/article/8dca14a7507443ccb3b0b8ddebc199c0
Autor:
Danuta Z. Loesch, Nicholas Trost, Minh Q. Bui, Eleanor Hammersley, Sui T. Lay, Sarah J. Annesley, Oana Sanislav, Claire Y. Allan, Flora Tassone, Zhi-Ping Chen, Kevin R. W. Ngoei, Bruce E. Kemp, David Francis, Paul R. Fisher, Elsdon Storey
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
The fragile X premutation (PM) allele contains a CGG expansion of 55–200 repeats in the FMR1 gene’s promoter. Male PM carriers have an elevated risk of developing neurological and psychiatric changes, including an approximately 50% risk of the fr
Externí odkaz:
https://doaj.org/article/ed047210fedd40acbad16fd88aea7db5
Publikováno v:
Colloid and Polymer Science. 300:1005-1015
Autor:
Amor, David E. Godler, Yoshimi Inaba, Minh Q. Bui, David Francis, Cindy Skinner, Charles E. Schwartz, David J.
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 13; Pages: 10712
This study characterizes the DNA methylation patterns specific to fragile X syndrome (FXS) with a full mutation (FM > 200 CGGs), premutation (PM 55–199 CGGs), and X inactivation in blood and brain tissues at the 3′ boundary of the FMR1 promoter.
Publikováno v:
Chemistry Letters. 51:368-371
Autor:
Danuta Z, Loesch, Flora, Tassone, George D, Mellick, Malcolm, Horne, Justin P, Rubio, Minh Q, Bui, David, Francis, Elsdon, Storey
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 33(7)
Background and Objective There is convincing evidence that small CGG expansion (41-54 repeats): FMR1 "gray zone" alleles (GZ) contribute to the risk of parkinsonism in males, but there is insufficient corresponding data in females. This study intends
Publikováno v:
IRC
One of the most vital aspects of navigation problem is path planning, in which we must be able to find the optimal path with minimum total transitions cost from the start to goal. This paper introduces the state-of-the-art D*Lite algorithm and presen