Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Mei Wang, Baker"'
Autor:
Jinkuk Hong, Robert S. Dembo, Leann Smith DaWalt, Mei Wang Baker, Elizabeth Berry-Kravis, Marsha R. Mailick
Publikováno v:
Cells, Vol 12, Iss 17, p 2137 (2023)
Higher education has been shown to have neuroprotective effects, reducing the risk of Alzheimer’s and Parkinson’s diseases, slowing the rate of age-related cognitive decline, and is associated with lower rates of early mortality. In the present s
Externí odkaz:
https://doaj.org/article/84212b94c74b4edfaaa220fa90e0ce1d
Publikováno v:
Frontiers in Psychiatry, Vol 12 (2021)
FMR1 CGG repeat length was assayed in 5499 research participants (2637 men and 2862 women) in the Wisconsin Longitudinal Study (WLS), a population-based cohort. Most past research has focused on clinically-ascertained individuals with expansions in C
Externí odkaz:
https://doaj.org/article/758cf89a24dc456b96f8cde21cea5133
Autor:
Marsha R. Mailick, Jinkuk Hong, Leann Smith DaWalt, Jan S. Greenberg, Arezoo Movaghar, Mei Wang Baker, Paul J. Rathouz, Murray H. Brilliant
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
The FMR1 gene on the X chromosome has varying numbers of CGG repeats. The modal number is 30, and expansion to >200 results in fragile X syndrome, but the copy number extends down to 6. Past research suggests that individuals whose CGGs are in the
Externí odkaz:
https://doaj.org/article/94e54bc9129e4949a87b4b2c7a65bc38
Publikováno v:
Frontiers in Psychiatry
FMR1 CGG repeat length was assayed in 5499 research participants (2637 men and 2862 women) in the Wisconsin Longitudinal Study (WLS), a population-based cohort. Most past research has focused on clinically-ascertained individuals with expansions in C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::611141115c100263d6be98a432375e35
https://pubmed.ncbi.nlm.nih.gov/34456771
https://pubmed.ncbi.nlm.nih.gov/34456771
Autor:
Nell Maltman, Leann Smith DaWalt, Jinkuk Hong, Mei Wang Baker, Elizabeth M. Berry-Kravis, Murray H. Brilliant, Marsha Mailick
Publikováno v:
American journal on intellectual and developmental disabilities. 128(1)
Variation in the FMR1 gene may affect aspects of cognition, such as executive function and memory. Environmental factors, such as stress, may also negatively impact cognitive functioning. Participants included 1,053 mothers of children with and witho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98231cc91a34190e69aad30039e4c05f
https://pubmed.ncbi.nlm.nih.gov/36548377
https://pubmed.ncbi.nlm.nih.gov/36548377
Autor:
Nell Maltman, Leann Smith DaWalt, Jinkuk Hong, Mei Wang Baker, Elizabeth M Berry-Kravis, Murray H. Brilliant, Marsha Mailick
Background: The FMR1 gene is essential for neural development and healthy synaptic function. The modal number of CGG repeats in FMR1 is 30, but the range is large with the reported copy number extending down to as few as 6 CGGs and up to over 200 CGG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa755ac82e7fdd61d2b5ce0f143290f3
https://doi.org/10.21203/rs.3.rs-18291/v2
https://doi.org/10.21203/rs.3.rs-18291/v2
Autor:
Arezoo, Movaghar, David, Page, Murray, Brilliant, Mei Wang, Baker, Jan, Greenberg, Jinkuk, Hong, Leann Smith, DaWalt, Krishanu, Saha, Finn, Kuusisto, Ron, Stewart, Elizabeth, Berry-Kravis, Marsha R, Mailick
Publikováno v:
Science Advances
Population screening and double-blind phenotyping confirm unique clinical profile in FMR1 premutation carriers.
The impact of the FMR1 premutation on human health is the subject of considerable controversy. A fundamental unanswered question is w
The impact of the FMR1 premutation on human health is the subject of considerable controversy. A fundamental unanswered question is w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad46f561894ed3bfb10c63530f8fd92a
https://pubmed.ncbi.nlm.nih.gov/31457090
https://pubmed.ncbi.nlm.nih.gov/31457090
Publikováno v:
American Journal of Medical Genetics. 108:1-6
Women who consume folic acid in early pregnancy reduced their risks for delivering offspring with neural tube defects (NTDs). The underlying process by which folic acid facilitated this risk reduction is unknown. Investigating genetic variation that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8f7a4393d31445e4f3652bd6f012972
https://doi.org/10.1002/ajmg.10195
https://doi.org/10.1002/ajmg.10195
Autor:
Gary M, Shaw, Edward J, Lammer, Huiping, Zhu, Mei Wang, Baker, Eric, Neri, Richard H, Finnell
Publikováno v:
American journal of medical genetics. 108(1)
Women who consume folic acid in early pregnancy reduced their risks for delivering offspring with neural tube defects (NTDs). The underlying process by which folic acid facilitated this risk reduction is unknown. Investigating genetic variation that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::addfe8ee7a472abdce59d37e07245096
https://pubmed.ncbi.nlm.nih.gov/11857541
https://pubmed.ncbi.nlm.nih.gov/11857541
Publikováno v:
American Journal of Medical Genetics. 113:392-392
The original article to which this Erratum refers was published in American Journal of Medical Genetics (2002) 108(1) 1–6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::542a983507fe153a3e3b58cb187d0dfd
https://doi.org/10.1002/ajmg.10986
https://doi.org/10.1002/ajmg.10986