Maciej P Golan
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Explore the profile of Maciej P Golan including associated specialties, affiliations and a list of published articles.
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8
Citations
64
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Recent Articles
1.
Augustyniak K, Lesniak M, Golan M, Latka H, Wojtan K, Zdanowski R, et al.
Int J Mol Sci
. 2024 Nov;
25(22).
PMID: 39596337
Adipocytes derived from 3T3-L1 cells are a gold standard for analyses of adipogenesis processes and the metabolism of fat cells. A widely used histological and immunohistochemical staining and mass spectrometry...
2.
Augustyniak K, Lesniak M, Latka H, Golan M, Kubiak J, Zdanowski R, et al.
J Lipid Res
. 2024 Jun;
65(7):100573.
PMID: 38844049
The full understanding of molecular mechanisms of cell differentiation requires a holistic view. Here we combine label-free FTIR and Raman hyperspectral imaging with data mining to detect the molecular cell...
3.
Wierzba-Bobrowicz T, Krajewski P, Tarka S, Acewicz A, Felczak P, Stepien T, et al.
Folia Neuropathol
. 2021 Oct;
59(3):219-231.
PMID: 34628787
Coronavirus disease 2019 (COVID-19) poses a global challenge to healthcare and society in the early 21st century. We report neuropathological changes in 52 patients aged between 22 years and 88...
4.
Golan M, Pilsyk S, Muszewska A, Wawrzyniak A
Bioessays
. 2020 Nov;
43(1):e2000207.
PMID: 33226145
Ferritins (FTs) are iron storage proteins that are involved in managing iron-oxygen balance. In our work, we present a hypothesis on the putative effect of geological changes that have affected...
5.
Pilsyk S, Mieczkowski A, Golan M, Wawrzyniak A, Kruszewska J
Int J Mol Sci
. 2020 Oct;
21(20).
PMID: 33086570
The gene encoding an alternative sulfate transporter was originally cloned from the genome of the Japanese isolate as a suppressor of sulfate permease-deficient strains. Expression of the gene is under...
6.
Golan M, Melquist S, Safranow K, Styczynska M, Slowik A, Kobrys M, et al.
Dement Geriatr Cogn Disord
. 2008 Mar;
25(4):366-71.
PMID: 18340109
Late-onset Alzheimer's disease (LOAD) is the most common neurodegenerative disorder, and has a complex etiology. Recently an intronic polymorphism in the ubiquilin 1 gene (UBQLN1) and a particular haplotype was...
7.
Maruszak A, Safranow K, Gacia M, Gabryelewicz T, Slowik A, Styczynska M, et al.
Dement Geriatr Cogn Disord
. 2007 Apr;
23(6):432-8.
PMID: 17457031
The sigma-1 receptor (SIGMAR1) is a subtype of a nonopioid sigma receptor family and is implicated in numerous functions connected with Alzheimer's disease (AD). Two common genetic variants were identified...
8.
Zekanowski C, Golan M, Krzysko K, Lipczynska-Lojkowska W, Filipek S, Kowalska A, et al.
Exp Neurol
. 2006 Mar;
200(1):82-8.
PMID: 16546171
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...