Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Grzegorz Rossa"'
Autor:
Wojciech Kozubski, Grzegorz Rossa, Grażyna Michałowska-Wender, Alicja Wawrzynek, Mieczysław Wender
Publikováno v:
Folia Neuropathologica. 4:417-420
Alzheimer disease (AD) is a complex, multi-factorial disease with the potential involvement of several genes. Alpha-2- macroglobulin (A2M) has been implicated in AD on the basis of its ability to mediate the clearance and degradation of -amyloid p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7b01db9ecccb92048f5399312a428b5
https://doi.org/10.5114/fn.2014.47842
https://doi.org/10.5114/fn.2014.47842
Autor:
Józef Szczech, Wojciech Kozubski, Anna Kowalska, Jolanta Florczak, Renata Modestowicz, Grzegorz Rossa, Danuta Pruchnik-Wolinska, Mieczysław Wender
Publikováno v:
Acta Biochimica Polonica. 51:245-252
A small number (1-5%) of Alzheimer's disease (AD) cases associated with the early-onset form of the disease (EOAD) appears to be transmitted as a pure genetic, autosomal dominant trait. To date, three genes responsible for familial EOAD have been ide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6122ff7e383500bd4922ef2b5d8b0feb
https://doi.org/10.18388/abp.2004_3617
https://doi.org/10.18388/abp.2004_3617
Autor:
Grażyna, Michałowska-Wender, Alicja, Wawrzynek, Grzegorz, Rossa, Wojciech, Kozubski, Mieczysław, Wender
Publikováno v:
Folia neuropathologica. 52(4)
Alzheimer disease (AD) is a complex, multi-factorial disease with the potential involvement of several genes. Alpha-2- macroglobulin (A2M) has been implicated in AD on the basis of its ability to mediate the clearance and degradation of -amyloid p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3f7a286b7867af34879acae44650af62
https://pubmed.ncbi.nlm.nih.gov/25574746
https://pubmed.ncbi.nlm.nih.gov/25574746
Autor:
Dorota Religa, Maria Barcikowska, Wanda Lipczyńska-Łojkowska, Grzegorz Rossa, Mieczysław Wender, Maria Styczyńska, Jerzy Kulczycki, Beata Pepłońska, Maciej P. Golan, Anna Kowalska, Cezary Żekanowski, Krystiana A. Krzyśko, Aleksandra Maruszak, Jacek Kuźnicki, Slawomir Filipek
Publikováno v:
Experimental neurology. 200(1)
Mutations in the amyloid precursor protein (APP), presenilin 1 (PSEN1) and presenilin 2 (PSEN2) genes are associated with early-onset familial Alzheimer's disease (EOAD). There are several reports describing mutations in PSEN1 in cases with frontotem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e64a76f826dda72cd9d8b69df37f1d32
https://pubmed.ncbi.nlm.nih.gov/16546171
https://pubmed.ncbi.nlm.nih.gov/16546171
Autor:
Anna, Kowalska, Danuta, Pruchnik-Wolińska, Jolanta, Florczak, Józef, Szczech, Wojciech, Kozubski, Grzegorz, Rossa, Mieczysław, Wender
Publikováno v:
Folia neuropathologica. 42(1)
The beta-amyloid precursor protein (APP) gene (on chromosome 21), Presenilin 1 (PS1) gene (on chromosome 14) and Presenilin 2 (PS2) gene (on chromosome 1) are responsible for autosomal dominant early-onset Alzheimer's disease (EOAD). Missense mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ed68ce83407d0d5bae13b1055323bf93
https://pubmed.ncbi.nlm.nih.gov/15119738
https://pubmed.ncbi.nlm.nih.gov/15119738
Autor:
Anna, Kowalska, Danuta, Pruchnik-Wolińska, Jolanta, Florczak, Józef, Szczech, Wojciech, Kozubski, Grzegorz, Rossa, Mieczysław, Wender
Publikováno v:
Folia neuropathologica. 42(1)
Mutations in Presenilin 1 (PS1) and Presenilin 2 (PS2) genes account for up to 50% of familial early-onset Alzheimer's disease (EOAD). In order to assess the genetic contribution of the PS genes in a series of Polish patients, we performed a mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7d3030fb69726f654ff643c2b10a601f
https://pubmed.ncbi.nlm.nih.gov/15119739
https://pubmed.ncbi.nlm.nih.gov/15119739
Autor:
Anna, Kowalska, Mieczyslaw, Wender, Jolanta, Florczak, Danuta, Pruchnik-Wolinska, Renata, Modestowicz, Józef, Szczech, Grzegorz, Rossa, Wojciech, Kozubski
Publikováno v:
Journal of applied genetics. 44(2)
Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by memory loss and personality changes. Pathological hallmarks of AD are: deposition of amyloid plaques and neurofibrillary tangles in the brain, accompanied by neuron
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c40b397360af237c6c9b5688d6cd6de1
https://pubmed.ncbi.nlm.nih.gov/12817569
https://pubmed.ncbi.nlm.nih.gov/12817569
Autor:
Grzegorz, Rossa
Publikováno v:
In Electroencephalography and Clinical Neurophysiology 1993 87(2):S76-S77