Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Brett A. DeMarco"'
Autor:
Anuj S. Jamenis, Tarun N. Bhatia, Kristin M. Miner, Krishna Kaku, Yesha Shah, Brett A. DeMarco, Rachel N. Clark, Aleem Gangjee, Rehana K. Leak
Publikováno v:
The FASEB Journal. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01af0040c0c16982a3be53006a2621c3
https://doi.org/10.1096/fasebj.2022.36.s1.r3222
https://doi.org/10.1096/fasebj.2022.36.s1.r3222
Autor:
Kristin M. Miner, Anuj S. Jamenis, Tarun N. Bhatia, Rachel N. Clark, Dhivyaa Rajasundaram, Sylvie Sauvaigo, Daniel M. Mason, Jessica M. Posimo, Nevil Abraham, Brett A. DeMarco, Xiaoming Hu, R. Anne Stetler, Jun Chen, Laurie H. Sanders, Kelvin C. Luk, Rehana K. Leak
Publikováno v:
Progress in neurobiology. 216
Lewy body disorders are characterized by oxidative damage to DNA and inclusions rich in aggregated forms of α-synuclein. Among other roles, apurinic/apyrimidinic endonuclease 1 (APE1) repairs oxidative DNA damage, and APE1 polymorphisms have been li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::354701835fd5f9b1d1b4c76692864fa6
https://pubmed.ncbi.nlm.nih.gov/35710046
https://pubmed.ncbi.nlm.nih.gov/35710046
Autor:
Gary J. Bassell, Allison Williams, Bart R. Anderson, Mihaela-Rita Mihailescu, Brett A. DeMarco, Snezana Stefanovic, Kathryn R. Moss
Publikováno v:
PLoS ONE
PLoS ONE, Vol 14, Iss 5, p e0217275 (2019)
PLoS ONE, Vol 14, Iss 5, p e0217275 (2019)
Fragile X syndrome, the most common inherited form of intellectual disability, is caused by the CGG trinucleotide expansion in the 5'-untranslated region of the Fmr1 gene on the X chromosome, which silences the expression of the fragile X mental reta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb04403301ef36ebe9b7a103b6a4f789
http://europepmc.org/articles/PMC6529005
http://europepmc.org/articles/PMC6529005
Publikováno v:
Biophysical Journal. 114:442a-443a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::011aab8bdcea0298d185e36ee1eee92d
https://doi.org/10.1016/j.bpj.2017.11.2447
https://doi.org/10.1016/j.bpj.2017.11.2447
Autor:
Brett A. DeMarco, Kathryn R. Williams, Snezana Stefanovic, Mihaela-Rita Mihailescu, Ayana Underwood, Gary J. Bassell
Publikováno v:
Molecular bioSystems. 11(12)
Fragile X syndrome, the most common cause of inherited intellectual disability, is caused by a trinucleotide CGG expansion in the 5'-untranslated region of the FMR1 gene, which leads to the loss of expression of the fragile X mental retardation prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d45e947b78c4f755aed5aeff441a62f
https://pubmed.ncbi.nlm.nih.gov/26412477
https://pubmed.ncbi.nlm.nih.gov/26412477
Autor:
Brett A. DeMarco
Publikováno v:
Biophysical Journal. (2):395a
Brain-derived neurotrophic factor (BDNF) is part of the neurotrophic family of genes that encodes for proteins that are known to promote survival of neurons in the peripheral and central nervous systems. The expression of the BDNF gene results in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38b1633e7907bf8d8bf8a065f5f83742