Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Thomas V, Burlin"'
Autor:
Kathleen C Schmidt, Inna Loutaev, Thomas V Burlin, Audrey Thurm, Carrie Sheeler, Carolyn Beebe Smith
Publikováno v:
Journal of Cerebral Blood Flow & Metabolism. 42:1666-1675
Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability. Fragile X mental retardation protein, a putative translation suppressor, is significantly reduced in FXS. The prevailing hypothesis is that rates of cerebral prot
Autor:
Kathleen C, Schmidt, Inna, Loutaev, Thomas V, Burlin, Audrey, Thurm, Carrie, Sheeler, Carolyn Beebe, Smith
Publikováno v:
J Cereb Blood Flow Metab
Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability. Fragile X mental retardation protein, a putative translation suppressor, is significantly reduced in FXS. The prevailing hypothesis is that rates of cerebral prot
Autor:
Shrinivas Bishu, Thomas V Burlin, Peter Herscovitch, Bik-Kee Vuong, Carolyn Beebe Smith, Michael A. Channing, Zhong-Hua Liu, Lisa M. Horowitz, Zengyan Xia, Zenaide M.N. Quezado, Aaron Unterman, Tianjiang Huang, Alan J. Zametkin, Mei Qin, Kathleen C Schmidt
Publikováno v:
Journal of Cerebral Blood Flow & Metabolism. 29:1035-1047
We report regional rates of cerebral protein synthesis (rCPS) in 10 healthy young males, each studied under two conditions: awake and anesthetized with propofol. We used the quantitative l-[1-11C]leucine positron emission tomography (PET) method to m
Autor:
Michael Kader, Mei Qin, Renate K. Hukema, Tianjian Huang, Carolyn Beebe Smith, Zhong-Hua Liu, Zachary Zeidler, Thomas V Burlin, Zengyan Xia
Publikováno v:
ASN Neuro, Vol 6 (2014)
ASN NEURO
ASN NEURO
The (CGG)n-repeat in the 5′-untranslated region of the fragile X mental retardation gene ( FMR1) gene is polymorphic and may become unstable on transmission to the next generation. In fragile X syndrome, CGG repeat lengths exceed 200, resulting in
Autor:
Tianjiang Huang, Lisa M. Horowitz, Carolyn Beebe Smith, Mei Qin, Shrinivas Bishu, Zengyan Xia, Kathleen C Schmidt, Zenaide M.N. Quezado, Thomas V Burlin, Alan J. Zametkin
Publikováno v:
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism. 33(4)
Dysregulated protein synthesis is thought to be a core phenotype of fragile X syndrome (FXS). In a mouse model ( Fmr1 knockout (KO)) of FXS, rates of cerebral protein synthesis (rCPS) are increased in selective brain regions. We hypothesized that rCP
Autor:
Aaron Unterman, Carolyn Beebe Smith, Peter Herscovitch, Zengyan Xia, Shrinivas Bishu, Zhong-Hua Liu, Shielah Conant, Tianjiang Huang, Kathleen C Schmidt, Mei Qin, Thomas V Burlin, Alan J. Zametkin, Michael A. Channing
We report regional rates of cerebral protein synthesis (rCPS) measured with the fully quantitative l-[1-11C]leucine positron emission tomography (PET) method. The method accounts for the fraction (Λ) of unlabeled amino acids in the precursor pool fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::827e5f66dd8934286aeb54aa72ebf4fe
https://europepmc.org/articles/PMC2775471/
https://europepmc.org/articles/PMC2775471/
Autor:
Zhong-Hua Liu, Thomas V Burlin, Michael A. Channing, Zengyan Xia, Tianjiang Huang, Mei Qin, Kathleen C Schmidt, Shrinivas Bishu, Bee Kee Vuong, Jeff Bacon, Carolyn Beebe Smith, Peter Herscovitch
Publikováno v:
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism. 28(7)
We have previously shown by direct comparison with autoradiographic and biochemical measurements that the l-[1-11C]leucine positron emission tomography method provides accurate determinations of regional rates of cerebral protein synthesis (rCPS) and
Autor:
Leland Krych, Tingrui Zhao, Zengyan Xia, Mei Qin, Carolyn Beebe Smith, Thomas V Burlin, Tianjian Huang, Zachary Zeidler, Michael Kader
Publikováno v:
International Journal of Neuropsychopharmacology
Background: Fragile X syndrome (FXS) is the most common known inherited form of intellectual disability and the single genomic cause of autism spectrum disorders. It is caused by the absence of a fragile X mental retardation gene ( Fmr1 ) product, FM
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience. 25(20)
Methylation-induced transcriptional silencing of the fragile X mental retardation-1 (Fmr1) gene leads to absence of the gene product, fragile X mental retardation protein (FMRP), and consequently fragile X syndrome (FrX), an X-linked inherited form o
Publikováno v:
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism. 25(5)
Measurements of regional rates of cerebral protein synthesis (rCPS) require correction for the effect of recycling of tissue amino acids back into the precursor pool for protein synthesis. The fraction of the precursor pool derived from arterial plas