Buchumschlag

Study of association between polymorphisms in the PSMB5 (rs11543947) and PSMA3 (rs2348071) genes and multiple sclerosis in Latvians

Functional realization of many signalling proteins and transcription factors implicated in the development and progression of multiple sclerosis is mediated by proteasomes. Aim of this case-control study was to evaluate genetic variations in the PSMB5 and PSMA3 genes encoding proteasomal subunits on...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Вiopolymers and Cell
Datum:	2014
Hauptverfasser:	Kalnina, J., Paramonova, N., Sjakste, N., Sjakste, T.
Format:	Artikel
Sprache:	Englisch
Veröffentlicht:	Інститут молекулярної біології і генетики НАН України 2014
Schlagworte:	Biomedicine
Online Zugang:	https://nasplib.isofts.kiev.ua/handle/123456789/154430
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!
Назва журналу:	Digital Library of Periodicals of National Academy of Sciences of Ukraine
Zitieren:	Study of association between polymorphisms in the PSMB5 (rs11543947) and PSMA3 (rs2348071) genes and multiple sclerosis in Latvians / J. Kalnina, N. Paramonova, N. Sjakste, T. Sjakste // Вiopolymers and Cell. — 2014. — Т. 30, № 4. — С. 305-309. — Бібліогр.: 31 назв. — англ.

Institution

Digital Library of Periodicals of National Academy of Sciences of Ukraine

Ähnliche Einträge

Study of association between polymorphisms in the PSMB5 (rs11543947) and PSMA3 (rs2348071) genes and multiple sclerosis in Latvians
von: J. Kalnina, et al.
Veröffentlicht: (2014)

Association between the PSMB5 and PSMC6 genetic variations and children obesity in the Latvian population
von: Paramonova, N., et al.
Veröffentlicht: (2014)

Association of the leukemia inhibitory factor gene polymorphism rs929271 with idiopathic mild intellectual disability
von: Gulkovskyi, R.V., et al.
Veröffentlicht: (2015)

Genetic variants in the PSMA6 , PSMC6 and PSMA3 genes associated with childhood asthma in Latvian and Taiwanese populations
von: N. Paramonova, et al.
Veröffentlicht: (2014)

Association between the PSMB5 and PSMC6 genetic variations and children obesity in the Latvian population
von: N. Paramonova, et al.
Veröffentlicht: (2014)

Association of the EPHA1 gene polymorphism with idiopathic mild intellectual disability
von: Gulkovskyi, R.V., et al.
Veröffentlicht: (2015)

Association of genetic polymorphism with the mutation status of the BRCA1/2 genes in spontanous breast cancer
von: Polinyk, S.I., et al.
Veröffentlicht: (2017)

Association of allelic polymorphisms of the Matrix Gla-protein system genes with acute coronary syndrome in the Ukrainian population
von: Garbuzova, V.Yu., et al.
Veröffentlicht: (2015)

The polymorphisms of genes involved in DNA methylation in patients with malignancies from West Ukraine
von: Dmytruk, I.M., et al.
Veröffentlicht: (2016)

Association of the leukemia inhibitory factor gene polymorphism rs929271 with idiopathic mild intellectual disability
von: R. V. Gulkovskyi, et al.
Veröffentlicht: (2015)

Association of genotypes by polymorphic variant C-108T of PON1 gene with the risk of developing breast cancer and hypertensive disease in women
von: Fishchuk, L.Ye.
Veröffentlicht: (2014)

T-138C polymorphism of MGP gene is associated with blood plasma cholesterol levels but not related to other risk factors of atherosclerosis in patients with ischemic stroke
von: Garbuzova, V.Yu., et al.
Veröffentlicht: (2014)

Evaluation of the RYR1 gene genetic diversity in the Latvian White pig breed
von: Dokāne, K., et al.
Veröffentlicht: (2016)

Evaluation of the RYR1 gene genetic diversity in the Latvian White pig breed
von: K. Dokāne, et al.
Veröffentlicht: (2016)

XRCC1 codon 399 polymorphism (RS25487) in the Ukrainian population
von: Ya. M. Mishchuk, et al.
Veröffentlicht: (2017)

Study on possible role of CYP1A1, GSTT1, GSTM1, GSTP1, NAT2 and ADRB2 genes polymorphisms in bronchial asthma development in children
von: Tatarskyy, P.F., et al.
Veröffentlicht: (2011)

Группы RS-автоматных преобразований
von: Олийнык, А.С.
Veröffentlicht: (2010)

Association of IL8 and IL10 gene allelic variants with ischemic stroke risk and prognosis
von: Kucherenko, A.M., et al.
Veröffentlicht: (2014)

The peculiarities of gene expression of medullary breast carcinoma tumor-associated antigens in different types of breast tumors
von: Shyian, А., et al.
Veröffentlicht: (2012)

Familial adenomatous polyposis: age of onset and association with mutations of the APC gene in patients from West Ukraine
von: Lozynska, M.R., et al.
Veröffentlicht: (2017)

EPHA1 gene SNPs analysis in population of Ukraine
von: Gulkovskyi, R.V., et al.
Veröffentlicht: (2013)

Multiple sclerosis
von: Palinskyy, I.Z.
Veröffentlicht: (2008)

The influence of GSTP1 A313G polymorphism on susceptibility, chemotherapy-related toxicity and prognosis of Hodgkin’s lymphoma in Ukrainian patients
von: Kriachok, I.A., et al.
Veröffentlicht: (2012)

Analysis of mutations in GBA gene in Ukrainian patients with Gaucher disease
von: Olkhovych, N.V., et al.
Veröffentlicht: (2017)

Development of ARMS PCR tests for detection of common CFTR gene mutations
von: Soloviov, O.O., et al.
Veröffentlicht: (2010)

Suppression of tumorigenicity and metastatic potential of melanoma cells by transduction of interferon gene
von: Lykhova, A.A., et al.
Veröffentlicht: (2014)

Contribution of chromosomal abnormalities and genes of the major histocompatibility complex to early pregnancy losses
von: Tkach, I.R., et al.
Veröffentlicht: (2015)

Association of TP53 Arg72Pro polymorphism (rs1042522) with bladder cancer risk in the Ukrainian population
von: Ya. M. Mishchuk, et al.
Veröffentlicht: (2018)

Study on occurrence of the IVS8-5T allele of the CFTR gene in Ukrainian males with spermatogenesis failure
von: Fesai, O.A., et al.
Veröffentlicht: (2010)

Novel gene PUS3 c.A212G mutation in Ukrainian family with intellectual disability
von: Gulkovskyi, R.V., et al.
Veröffentlicht: (2015)

Identification of genotypes with recombinant arm 1RS in bread wheat segregating F5 populations from crosses between carriers of 1BL.1RS AND 1AL.1RS
von: N. O. Kozub, et al.
Veröffentlicht: (2022)

Molecular-genetic characterization of Ukrainian patients with mucopolysaccharidosis IIIA: identification of three new mutations in the heparan-N-sulfatase gene
von: Trofimova, N.S., et al.
Veröffentlicht: (2016)

Molecular-genetic characterization of Ukrainian patients with mucopolysaccharidosis I: identification of three new mutations in α-L-iduronidase gene
von: Trofimova, N.S., et al.
Veröffentlicht: (2016)

PPM1M and PRICKLE2 are potential tumor suppressor genes in human clear-cell renal cell carcinoma
von: Rudenko, E.E., et al.
Veröffentlicht: (2014)

Z*-semilocal modules and the proper class RS
von: E. Tьrkmen
Veröffentlicht: (2019)

Multiple-field interstitial photodynamic therapy of subcutaneously transplanted cholangiocellular carcinoma RS-1 in rats
von: Tzerkovsky, D.A.
Veröffentlicht: (2017)

IFN-l-3 (IL28B) genotyping by restriction fragment length polymorphism method: detection polymorphism of rs12979860
von: Pampukha, V.M., et al.
Veröffentlicht: (2011)

Protooncogene MDM2 SNP309 (rs2279744) analysis of polymorphism in thyroid cancer: Pakistani population
von: M. S. Iqbal, et al.
Veröffentlicht: (2022)

Ischemic stroke in Ukrainian population: possible involvement of the F2 G20210A, F5 G1691A and MTHFR C677T gene variants
von: Tatarskyy, P.F., et al.
Veröffentlicht: (2010)

Association between XPO5 rs11077 polymorphism and cancer susceptibility: a meta-analysis of 7284 cases and 8511 controls
von: Moazeni-Roodi, A., et al.
Veröffentlicht: (2023)