199 related articles for article (PubMed ID: 30413149)
1. ENHO, RXRA, and LXRA polymorphisms and dyslipidaemia, related comorbidities and survival in haemodialysis patients.
Grzegorzewska AE; Niepolski L; Świderska MK; Mostowska A; Stolarek I; Warchoł W; Figlerowicz M; Jagodziński PP
BMC Med Genet; 2018 Nov; 19(1):194. PubMed ID: 30413149
[TBL] [Abstract][Full Text] [Related]
2. Calcium-sensing receptor gene (CASR) polymorphisms and CASR transcript level concerning dyslipidemia in hemodialysis patients: a cross-sectional study.
Grzegorzewska AE; Frycz BA; Świderska M; Niepolski L; Mostowska A; Jagodziński PP
BMC Nephrol; 2019 Nov; 20(1):436. PubMed ID: 31775661
[TBL] [Abstract][Full Text] [Related]
3. Involvement of adropin and adropin-associated genes in metabolic abnormalities of hemodialysis patients.
Grzegorzewska AE; Niepolski L; Mostowska A; Warchoł W; Jagodziński PP
Life Sci; 2016 Sep; 160():41-46. PubMed ID: 27449397
[TBL] [Abstract][Full Text] [Related]
4. T-cell cytokine gene polymorphisms and vitamin D pathway gene polymorphisms in end-stage renal disease due to type 2 diabetes mellitus nephropathy: comparisons with health status and other main causes of end-stage renal disease.
Grzegorzewska AE; Ostromecki G; Zielińska P; Mostowska A; Jagodziński PP
J Diabetes Res; 2014; 2014():120317. PubMed ID: 25587543
[TBL] [Abstract][Full Text] [Related]
5. Antibodies to hepatitis B virus surface antigen and interleukin 12 and interleukin 18 gene polymorphisms in hemodialysis patients.
Grzegorzewska AE; Wobszal PM; Mostowska A; Jagodziński PP
BMC Nephrol; 2012 Aug; 13():75. PubMed ID: 22863216
[TBL] [Abstract][Full Text] [Related]
6. Polymorphisms of T helper cell cytokine-associated genes and survival of hemodialysis patients - a prospective study.
Grzegorzewska AE; Świderska MK; Mostowska A; Warchoł W; Jagodziński PP
BMC Nephrol; 2017 May; 18(1):165. PubMed ID: 28525983
[TBL] [Abstract][Full Text] [Related]
7. Association of Retinoid X Receptor Alpha Gene Polymorphism with Clinical Course of Chronic Glomerulonephritis.
Grzegorzewska AE; Ostromecki G; Zielińska P; Mostowska A; Niemir Z; Polcyn-Adamczak M; Pawlik M; Sowińska A; Jagodziński PP
Med Sci Monit; 2015 Nov; 21():3671-81. PubMed ID: 26610845
[TBL] [Abstract][Full Text] [Related]
8. Liver X receptor α gene polymorphisms and variable cardiovascular outcomes in patients treated with antihypertensive therapy: results from the INVEST-GENES study.
Price ET; Pacanowski MA; Martin MA; Cooper-DeHoff RM; Pepine CJ; Zineh I; Johnson JA
Pharmacogenet Genomics; 2011 Jun; 21(6):333-40. PubMed ID: 21562465
[TBL] [Abstract][Full Text] [Related]
9. Enho Mutations Causing Low Adropin: A Possible Pathomechanism of MPO-ANCA Associated Lung Injury.
Gao F; Fang J; Chen F; Wang C; Chen S; Zhang S; Lv X; Zhang J; He Q; Weng S; Liu Q; Lin XH
EBioMedicine; 2016 Jul; 9():324-335. PubMed ID: 27333037
[TBL] [Abstract][Full Text] [Related]
10. Association between the rs2279238 of the Liver X receptor alpha gene polymorphism and advanced carotid atherosclerosis in the Slovenian cohort.
Grbić E; Gorkič N; Pleskovič A; Ljuca F; Gasparini M; Mrđa B; Cilenšek I; Fras Z; Petrovič D
Gene; 2022 Oct; 840():146764. PubMed ID: 35907563
[TBL] [Abstract][Full Text] [Related]
11. Titers of antibodies to the surface antigen of hepatitis B virus after vaccination in relation to immunity-related gene variants. A prospective study among hemodialysis patients.
Jodłowska-Siewert E; Jagodziński PP; Grzegorzewska AE
Pol Arch Intern Med; 2017 Aug; 127(7-8):481-489. PubMed ID: 28817541
[TBL] [Abstract][Full Text] [Related]
12. Serum adropin level and ENHO gene expression in systemic sclerosis.
Yolbas S; Kara M; Yilmaz M; Aydin S; Koca SS
Clin Rheumatol; 2016 Jun; 35(6):1535-40. PubMed ID: 27079850
[TBL] [Abstract][Full Text] [Related]
13. Adropin: An endocrine link between the biological clock and cholesterol homeostasis.
Ghoshal S; Stevens JR; Billon C; Girardet C; Sitaula S; Leon AS; Rao DC; Skinner JS; Rankinen T; Bouchard C; Nuñez MV; Stanhope KL; Howatt DA; Daugherty A; Zhang J; Schuelke M; Weiss EP; Coffey AR; Bennett BJ; Sethupathy P; Burris TP; Havel PJ; Butler AA
Mol Metab; 2018 Feb; 8():51-64. PubMed ID: 29331507
[TBL] [Abstract][Full Text] [Related]
14. Paraoxonase 1 concerning dyslipidaemia, cardiovascular diseases, and mortality in haemodialysis patients.
Grzegorzewska AE; Adamska P; Iwańczyk-Skalska E; Ostromecka K; Niepolski L; Marcinkowski W; Mostowska A; Warchoł W; Żaba C; Jagodziński PP
Sci Rep; 2021 Mar; 11(1):6773. PubMed ID: 33762698
[TBL] [Abstract][Full Text] [Related]
15. ENHO gene expression and serum adropin level in rheumatoid arthritis and systemic lupus erythematosus.
Yolbas S; Kara M; Kalayci M; Yildirim A; Gundogdu B; Aydin S; Koca SS
Adv Clin Exp Med; 2018 Dec; 27(12):1637-1641. PubMed ID: 30141839
[TBL] [Abstract][Full Text] [Related]
16. Genetic variants in the vitamin D pathway and breast cancer disease-free survival.
Pande M; Thompson PA; Do KA; Sahin AA; Amos CI; Frazier ML; Bondy ML; Brewster AM
Carcinogenesis; 2013 Mar; 34(3):587-94. PubMed ID: 23180655
[TBL] [Abstract][Full Text] [Related]
17. Single nucleotide polymorphisms in LCAT may contribute to dyslipidaemia in HIV-infected individuals on HAART in a Ghanaian population.
Bani SB; Danquah KO; Obirikorang C; Owiredu WKBA; Quaye L; Muonir Der E; Acheampong E; Adams Y; Dapare PPM; Banyeh M; Anto EO; Sakyi SA
Sci Rep; 2020 Nov; 10(1):19419. PubMed ID: 33173066
[TBL] [Abstract][Full Text] [Related]
18. Higher atherogenic risk in schoolchildren is associated with MTMR9 rs2293855 gene polymorphism and genetic score.
Silva MA; Resende CMM; Louro MB; Ribeiro SAV; do Carmo Castro Franceschini S; Velasquez-Melendez G; Alvarez-Leite JI; Durso DF; de Novaes JF
Nutr Bull; 2023 Dec; 48(4):559-571. PubMed ID: 37905391
[TBL] [Abstract][Full Text] [Related]
19. Polymorphisms of Vitamin D Signaling Pathway Genes and Calcium-Sensing Receptor Gene in respect to Survival of Hemodialysis Patients: A Prospective Observational Study.
Grzegorzewska AE; Świderska MK; Mostowska A; Warchoł W; Jagodziński PP
Int J Endocrinol; 2016; 2016():2383216. PubMed ID: 27642296
[TBL] [Abstract][Full Text] [Related]
20. T helper cell‑related cytokine gene polymorphisms and vitamin D pathway gene polymorphisms as predictors of survival probability in patients on renal replacement therapy.
Świderska M; Mostowska A; Grzegorzewska AE
Pol Arch Med Wewn; 2015; 125(7-8):511-20. PubMed ID: 26039912
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
