Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Monika, Sieruta"'
Autor:
Ewa Golanska, Agata Gajos, Monika Sieruta, Malgorzata Szybka, Monika Rudzinska, Stanislaw Ochudlo, Tomasz Kmiec, Pawel P Liberski, Andrzej Bogucki
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0129656 (2015)
The aim of this study was to assess the presence of DYT6 mutations in Polish patients with isolated dystonia and to characterize their phenotype. We sequenced THAP1 exons 1, 2 and 3 including exon-intron boundaries and 5'UTR fragment in 96 non-DYT1 d
Externí odkaz:
https://doaj.org/article/293ed659961f4564a2750e132880bd8f
Autor:
Ewa Golanska, Malgorzata Szybka, Pawel P. Liberski, Monika Sieruta, Agata Gajos, Andrzej Bogucki
Publikováno v:
International Journal of Neuroscience. 125:755-759
Mutations in the THAP1 gene are associated with a broad spectrum of dystonia including focal and generalized forms. Missense, nonsense and frameshift mutations, including small insertions/deletions within the THAP1 gene, have been reported and majori
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bffad6985b3cfc6a941c84effa2c2d2
https://doi.org/10.3109/00207454.2014.981749
https://doi.org/10.3109/00207454.2014.981749
Autor:
Pawel P. Liberski, Elizabeth H. Corder, Maria Barcikowska, Sylwia M. Gresner, Ewa Golanska, Anna Pfeffer, Małgorzata Mossakowska, Tomasz Sobów, Aleksandra Szybinska, Monika Sieruta, Izabela Klich, Malgorzata Chodakowska-Zebrowska
Publikováno v:
Prion. 7:244-247
The PRNP gene encodes the cellular isoform of prion protein (PrP (c) ). The M129V polymorphism influences the risk of prion diseases and may modulate the rate of neurodegeneration with age. We present the first study of the polymorphism among Polish
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb90b85eaddb42f8e9a2e0bd135b1249
https://doi.org/10.4161/pri.23903
https://doi.org/10.4161/pri.23903
Autor:
Izabela Zawlik, Tomasz Sobów, Pawel P. Liberski, Krystyna Hulas-Bigoszewska, Beata Pepłońska, Monika Sieruta, Maria Barcikowska, Elizabeth H. Corder, Maria Styczyńska, Sylwia M. Gresner, Monika Witusik, Ewa Golanska
Publikováno v:
Journal of Alzheimer's Disease. 17:359-368
We studied eight polymorphisms within APOE, PRNP, PRND, and CYP46 genes in 213 Polish late-onset patients with Alzheimer's disease (AD) and 171 non-demented elderly controls. A latent classification approach, grade-of-membership analysis, was taken t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af031e0eeeef759c462fd5fef630bd8f
https://doi.org/10.3233/jad-2009-1055
https://doi.org/10.3233/jad-2009-1055
Autor:
Sylwester Piaskowski, Pawel P. Liberski, Robert Stawski, Piotr Rieske, Dariusz J. Jaskólski, Wielisław Papierz, Ewelina Stoczynska-Fidelus, Malgorzata Szybka, M. Wolanczyk, Monika Sieruta, Michał Bieńkowski
Publikováno v:
British Journal of Cancer
Background: It has recently been reported by several sources that original (i.e., present in vivo) glioma cell phenotypes or genotypes cannot be maintained in vitro. For example, glioblastoma cell lines presenting EGFR amplification cannot be establi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca2ebf7842253c99e70f86119bafedc4
https://doi.org/10.1038/bjc.2011.27
https://doi.org/10.1038/bjc.2011.27
Autor:
Ewa Golanska, Krystyna Hulas-Bigoszewska, Sylwia M. Gresner, Beata Pepłońska, Maria Styczyńska, Maria Barcikowska, Pawel P. Liberski, Monika Sieruta, Elizabeth H. Corder
Publikováno v:
Neuroscience Letters. 447:164-166
The accumulation of beta-amyloid (Abeta) in the brain plays a central role in the pathogenesis of Alzheimer's disease (AD). The processing of Abeta precursor protein to Abeta is modulated by binding proteins including APBB2 [amyloid beta precursor pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3737e2709d02544013a7a272344306c2
https://doi.org/10.1016/j.neulet.2008.10.003
https://doi.org/10.1016/j.neulet.2008.10.003
Autor:
Ryszard Jaszewski, Andrzej Banys, Tomasz Sobów, Jakub Kazmierski, Iwona Kłoszewska, Monika Sieruta, Pawel P. Liberski
Publikováno v:
General hospital psychiatry. 36(6)
Objective The studies regarding the role of genes polymorphism in development of postoperative delirium are extremely rare. Therefore, we investigated the potential association of polymorphism in 5HT2a receptor gene and N -methyl-d-aspartate (NMDA) r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1b8f549e6846d5ed085371d63f6e9b3
https://pubmed.ncbi.nlm.nih.gov/25041634
https://pubmed.ncbi.nlm.nih.gov/25041634
Autor:
Anna Pfeffer, Maria Barcikowska, Malgorzata Chodakowska-Zebrowska, Sylwia M. Gresner, Tomasz Sobów, Aleksandra Szybinska, Izabela Klich, Pawel P. Liberski, Małgorzata Mossakowska, Ewa Golanska, Monika Sieruta
Publikováno v:
Experimental gerontology. 48(4)
APBB2 gene encodes for β-amyloid precursor protein-binding family B member 2, (APBB2, FE65-like, FE65L1), an adaptor protein binding to the cytoplasmatic domain of β-amyloid precursor protein (βAPP). Over-expression of APBB2 promotes formation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ad873247fff51d8247d61a9d9aa3fd6
https://pubmed.ncbi.nlm.nih.gov/23384821
https://pubmed.ncbi.nlm.nih.gov/23384821
Autor:
Monika Sieruta, Pawel P. Liberski, Iwona Kłoszewska, Marcin Flirski, Ewa Golanska, Tomasz Sobów
Publikováno v:
Prion. 6(1)
The etiology of behavioral and psychological symptoms of dementia (BPSD) is complex, including putative biological, psychological, social and environmental factors. Recent years have witnessed accumulation of data on the association between genetic f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1913e82ee76c4c9156dc94b1dc0eb3c7
https://pubmed.ncbi.nlm.nih.gov/22453181
https://pubmed.ncbi.nlm.nih.gov/22453181
Publikováno v:
Neurologia i neurochirurgia polska. 42(5)
There are no non-invasive tests allowing for definite premortem diagnosis of Creutzfeldt-Jakob disease (CJD). The paper presents the current knowledge about laboratory tests supporting CJD diagnosis. 14-3-3 protein in the cerebrospinal fluid is the o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d63d6eca78c4bc630bed88e5c0a76e25
https://pubmed.ncbi.nlm.nih.gov/19105113
https://pubmed.ncbi.nlm.nih.gov/19105113