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Items: 1 to 20 of 67

1.

[Investigating the role of ceramide metabolism-associated CERS5 (LASS5) gene in atherosclerosis pathogenesis in endothelial cells].

Çoban N, Güçlü Geyik F, Yıldırım Ö, Erginel Ünaltuna N.

Turk Kardiyol Dern Ars. 2017 Mar;45(2):118-125. doi: 10.5543/tkda.2016.82389. Turkish.

2.

Identification of potential target genes of ROR-alpha in THP1 and HUVEC cell lines.

Gulec C, Coban N, Ozsait-Selcuk B, Sirma-Ekmekci S, Yildirim O, Erginel-Unaltuna N.

Exp Cell Res. 2017 Apr 1;353(1):6-15. doi: 10.1016/j.yexcr.2017.02.028. Epub 2017 Feb 24.

PMID:
28238834
3.

Role of simvastatin and RORα activity in the macrophage apoptotic pathway.

Çoban N, Güleç Ç, Özsait Selçuk B, Erginel-Ünaltuna N.

Anatol J Cardiol. 2017 Feb 1. doi: 10.14744/AnatolJCardiol.2016.7411. [Epub ahead of print]

4.

CYP19A1, MIF and ABCA1 genes are targets of the RORα in monocyte and endothelial cells.

Coban N, Gulec C, Ozsait-Selcuk B, Erginel-Unaltuna N.

Cell Biol Int. 2017 Feb;41(2):163-176. doi: 10.1002/cbin.10712.

PMID:
27925372
5.

Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients.

Guven G, Lohmann E, Bras J, Gibbs JR, Gurvit H, Bilgic B, Hanagasi H, Rizzu P, Heutink P, Emre M, Erginel-Unaltuna N, Just W, Hardy J, Singleton A, Guerreiro R.

PLoS One. 2016 Sep 15;11(9):e0162592. doi: 10.1371/journal.pone.0162592. eCollection 2016.

6.

Risk of obesity and metabolic syndrome associated with FTO gene variants discloses clinically relevant gender difference among Turks.

Guclu-Geyik F, Onat A, Yuzbasıogulları AB, Coban N, Can G, Lehtimäki T, Erginel-Unaltuna N.

Mol Biol Rep. 2016 Jun;43(6):485-94. doi: 10.1007/s11033-016-3992-0. Epub 2016 May 4.

PMID:
27146691
7.

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.

Lesage S, Drouet V, Majounie E, Deramecourt V, Jacoupy M, Nicolas A, Cormier-Dequaire F, Hassoun SM, Pujol C, Ciura S, Erpapazoglou Z, Usenko T, Maurage CA, Sahbatou M, Liebau S, Ding J, Bilgic B, Emre M, Erginel-Unaltuna N, Guven G, Tison F, Tranchant C, Vidailhet M, Corvol JC, Krack P, Leutenegger AL, Nalls MA, Hernandez DG, Heutink P, Gibbs JR, Hardy J, Wood NW, Gasser T, Durr A, Deleuze JF, Tazir M, Destée A, Lohmann E, Kabashi E, Singleton A, Corti O, Brice A; French Parkinson's Disease Genetics Study (PDG).; International Parkinson's Disease Genomics Consortium (IPDGC)..

Am J Hum Genet. 2016 Mar 3;98(3):500-13. doi: 10.1016/j.ajhg.2016.01.014.

8.

Lipoprotein(a) level and MIF gene variant predict incident metabolic syndrome and mortality.

Onat A, Can G, Çoban N, Dönmez İ, Çakır H, Ademoğlu E, Erginel-Ünaltuna N, Yüksel H.

J Investig Med. 2016 Feb;64(2):392-9. doi: 10.1136/jim-2015-000003.

PMID:
26911630
9.

Sex- and Obesity-specific Association of Aromatase (CYP19A1) Gene Variant with Apolipoprotein B and Hypertension.

Coban N, Onat A, Guclu-Geyik F, Can G, Erginel-Unaltuna N.

Arch Med Res. 2015 Oct;46(7):564-71. doi: 10.1016/j.arcmed.2015.09.004. Epub 2015 Sep 26.

PMID:
26415088
10.

A new F-box protein 7 gene mutation causing typical Parkinson's disease.

Lohmann E, Coquel AS, Honoré A, Gurvit H, Hanagasi H, Emre M, Leutenegger AL, Drouet V, Sahbatou M, Guven G, Erginel-Unaltuna N, Deleuze JF, Lesage S, Brice A.

Mov Disord. 2015 Jul;30(8):1130-3. doi: 10.1002/mds.26266. Epub 2015 May 23.

PMID:
26010069
11.

Clinical variability in ataxia-telangiectasia.

Lohmann E, Krüger S, Hauser AK, Hanagasi H, Guven G, Erginel-Unaltuna N, Biskup S, Gasser T.

J Neurol. 2015 Jul;262(7):1724-7. doi: 10.1007/s00415-015-7762-z. Epub 2015 May 10.

PMID:
25957637
12.

Negative results in screening for possible new sequence variations on ATP-binding cassette transporter A1 gene in Turkish adults with metabolic syndrome.

Çoban N, Onat A, Geyik F, Erginel Ünaltuna N.

Turk Kardiyol Dern Ars. 2014 Sep;42(6):524-30. doi: 10.5543/tkda.2014.64369.

13.

Low "quotient" Lp(a) concentration mediates autoimmune activation and independently predicts cardiometabolic risk.

Onat A, Çoban N, Can G, Yüksel M, Karagöz A, Yüksel H, Ademoğlu E, Erginel-Ünaltuna N.

Exp Clin Endocrinol Diabetes. 2015 Jan;123(1):11-8. doi: 10.1055/s-0034-1385922. Epub 2014 Oct 14.

PMID:
25314652
14.

Oxidative stress-mediated (sex-specific) loss of protection against type-2 diabetes by macrophage migration inhibitory factor (MIF)-173G/C polymorphism.

Coban N, Onat A, Yildirim O, Can G, Erginel-Unaltuna N.

Clin Chim Acta. 2015 Jan 1;438:1-6. doi: 10.1016/j.cca.2014.07.037. Epub 2014 Aug 6.

PMID:
25108206
15.

Association between non-coding polymorphisms of HOPX gene and syncope in hypertrophic cardiomyopathy.

Güleç Ç, Abacı N, Bayrak F, Kömürcü Bayrak E, Kahveci G, Güven C, Erginel Ünaltuna N.

Anadolu Kardiyol Derg. 2014 Nov;14(7):617-24. doi: 10.5152/akd.2014.4972. Epub 2014 Feb 10.

16.

Prevalence of Prader-Willi syndrome among infants with hypotonia.

Tuysuz B, Kartal N, Erener-Ercan T, Guclu-Geyik F, Vural M, Perk Y, Erçal D, Erginel-Unaltuna N.

J Pediatr. 2014 May;164(5):1064-7. doi: 10.1016/j.jpeds.2014.01.039. Epub 2014 Feb 25.

PMID:
24582009
17.

Gender-specific associations of the APOA1 -75G>A polymorphism with several metabolic syndrome components in Turkish adults.

Coban N, Onat A, Guclu-Geyik F, Komurcu-Bayrak E, Can G, Erginel-Unaltuna N.

Clin Chim Acta. 2014 Apr 20;431:244-9. doi: 10.1016/j.cca.2014.01.017. Epub 2014 Feb 6.

PMID:
24508624
18.

Gender specific association of ABCA1 gene R219K variant in coronary disease risk through interactions with serum triglyceride elevation in Turkish adults.

Çoban N, Onat A, Kömürcü Bayrak E, Güleç Ç, Can G, Erginel Ünaltuna N.

Anadolu Kardiyol Derg. 2014 Feb;14(1):18-25. doi: 10.5152/akd.2013.234. Epub 2013 Sep 26.

19.

TREM2 variants in Alzheimer's disease.

Guerreiro R, Wojtas A, Bras J, Carrasquillo M, Rogaeva E, Majounie E, Cruchaga C, Sassi C, Kauwe JS, Younkin S, Hazrati L, Collinge J, Pocock J, Lashley T, Williams J, Lambert JC, Amouyel P, Goate A, Rademakers R, Morgan K, Powell J, St George-Hyslop P, Singleton A, Hardy J; Alzheimer Genetic Analysis Group..

N Engl J Med. 2013 Jan 10;368(2):117-27. doi: 10.1056/NEJMoa1211851. Epub 2012 Nov 14.

20.

High serum apolipoprotein E determines hypertriglyceridemic dyslipidemias, coronary disease and apoA-I dysfunctionality.

Onat A, Can G, Ornek E, Ayhan E, Erginel-Ünaltuna N, Murat SN.

Lipids. 2013 Jan;48(1):51-61. doi: 10.1007/s11745-012-3724-8. Epub 2012 Oct 25.

PMID:
23096223

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