Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Maja Dinekov"'
Publikováno v:
Neurobiology of Disease, Vol 147, Iss , Pp 105138- (2021)
Neurofibrillary tangles arising from aggregated microtubule-associated protein tau occur in aged brains and are hallmarks of neurodegenerative diseases. A subset of neurons containing aggregated tau displays granulovacuolar degeneration (GVD) that is
Externí odkaz:
https://doaj.org/article/44939331410240dab3bd2af71581d43a
Publikováno v:
Neurobiology of Disease, Vol 71, Iss , Pp 169-179 (2014)
Histopathological studies on the brains of tauopathy cases including cases with Alzheimer's disease (AD) demonstrate that neurons with hyperphosphorylated protein tau display granulovacuolar degeneration (GVD), as evidenced by vacuolar lesions harbor
Externí odkaz:
https://doaj.org/article/83da5854e37b461c830701d832b3a10e
Publikováno v:
Clinical anatomy 35(3), 404-411 (2022). doi:10.1002/ca.23846
Clinical anatomy 35(3), 404-411 (2022). doi:10.1002/ca.23846
Published by Wiley, New York, NY [u.a.]
Published by Wiley, New York, NY [u.a.]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bbb7c93625034b6ffd37e7d254b9f24
Publikováno v:
Neurobiology of Disease, Vol 147, Iss, Pp 105138-(2021)
Neurofibrillary tangles arising from aggregated microtubule-associated protein tau occur in aged brains and are hallmarks of neurodegenerative diseases. A subset of neurons containing aggregated tau displays granulovacuolar degeneration (GVD) that is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e27c012d30c2be6bdace3370958c516
https://pubmed.ncbi.nlm.nih.gov/33069844
https://pubmed.ncbi.nlm.nih.gov/33069844
Publikováno v:
Brain research. 1706
Charged multivesicular body protein 2b (CHMP2B) is a subunit of the endosomal sorting complex required for transport (ESCRT)-III that mediates scission of budded membranes. Neurons with CHMP2B-positive granulovacuolar inclusions in the cytoplasm are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19bcf90aa442721cfe44c6c0e78d768c
https://pubmed.ncbi.nlm.nih.gov/30414727
https://pubmed.ncbi.nlm.nih.gov/30414727
Publikováno v:
Brain research. 1677
Purpose Spleen tyrosine kinase (Syk) has been shown to phosphorylate tyrosine 18 of tau in vitro. It has been proposed that increased immunoreactivity for double-phosphorylated Syk in hippocampal neurons of Alzheimer’s disease cases indicates a not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::258575da18385f3ec1db6ed32bea7dbe
https://pubmed.ncbi.nlm.nih.gov/28919467
https://pubmed.ncbi.nlm.nih.gov/28919467
Publikováno v:
Brain research. 1659
We examined the distribution pattern of the phosphorylated 40S ribosomal subunit protein S6, a downstream target of the mTOR pathway, in the brains of 24-months-old human tau transgenic pR5 mice, non-transgenic littermates and in human hippocampi. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14aa9d1ae9cc74b8e4163b707dec13b9
https://pubmed.ncbi.nlm.nih.gov/28119058
https://pubmed.ncbi.nlm.nih.gov/28119058
Publikováno v:
Neurobiology of Disease, Vol 71, Iss, Pp 169-179 (2014)
Histopathological studies on the brains of tauopathy cases including cases with Alzheimer's disease (AD) demonstrate that neurons with hyperphosphorylated protein tau display granulovacuolar degeneration (GVD), as evidenced by vacuolar lesions harbor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67fad307a8c2c99869402efae67067ba
https://pubmed.ncbi.nlm.nih.gov/25073087
https://pubmed.ncbi.nlm.nih.gov/25073087
Publikováno v:
Neurobiology of aging. 34(5)
We studied underlying pathomechanisms in tauopathies using pR5 mice that express the P301L tau mutation found in familial forms of frontotemporal dementia. In a longitudinal study we investigated the functional status of glycogen synthase kinase-3 an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b92a499d91dc225b63514d2c23acb7d5
https://pubmed.ncbi.nlm.nih.gov/23294633
https://pubmed.ncbi.nlm.nih.gov/23294633