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Nihan Erginel‐Ünaltuna

universite de lille

24H指数
155论文数
1.9K被引数
收录论文 40
发表时间
A patient with early-onset Alzheimer's disease with a novel PSEN1 p.Leu424Pro mutation
err2019-12-01
err4
PREAI
errGuven, Gamze; Erginel-Unaltuna, Nihan; Samanci, Bedia; Gulec, Cagri; Hanagasi, Hasmet; Bilgic, Basar
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AMPK ACTIVATION DECREASES EXPRESSION OF MIR-130B IN ENDOTHELIAL CELLS
err2019-08-01
err0
PREAI
errCoban, N.; Ozuynuk, A. S.; Erginel-Unaltuna, N.
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CORONARY ARTERY DISEASE RELATED MIR-19A AND MIR-26A ARE SENSITIVE TO SIMVASTATIN AND ROR-ALPHA LIGANDS IN MACROPHAGE CELLS
err2019-08-01
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PREAI
errCoban, N.; Gulec, C.; Ozuynuk, A. S.; Erginel-Unaltuna, N.; Erkan, A. F.
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IDENTIFICATION OF MIRNA PROFILING IN EPICARDIAL ADIPOSE TISSUE OF PATIENTS WITH ATHEROSCLEROSIS
err2019-08-01
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PREAI
errGuclu-Geyik, F.; Koseoglu, P.; Ozsoy, S. D.; Cetin, H. K.; Balkanay, O. O.; Yildiz, C. E.; Goksedef, D.; Coban, N.; Komurcu-Bayrak, A. E.; Erginel-Unaltuna, N.
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Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal Dementia
err2019-01-08
err10
errOAAI
errGuven, Gamze; Bilgic, Briar; Tufekcioglu, Zeynep; Unaltuna, Nihan Erginel; Hanagasi, Hasmet; Gurvit, Hakan; Singleton, Andrew; Hardy, John; Emre, Murat; Gulec, Cagri; Bras, Jose; Guerreiro, Rita; Lohmann, Ebba
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HPCA Confirmed as a Genetic Cause of DYT2-Like Dystonia Phenotype
err2018-08-25
err26
PREAI
errAtasu, Burcu; Hanagasi, Hasmet; Bilgic, Basar; Pak, Meltem; Erginel-Unaltuna, Nihan; Hauser, Ann-Kathrin; Guven, Gamze; Simon-Sanchez, Javier; Heutink, Peter; Gasser, Thomas; Lohmann, Ebba
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A NOVEL MIRSNP AT THE IGF1 3′UTR MAY MODULATE THE MIRNA-MEDIATED GENE EXPRESSION IN CARDIOVASCULAR DISEASE
err2018-08-01
err0
PREAI
errPirim, D.; Coban, N.; Erkan, A. F.; Ekici, B.; Erginel-Unaltuna, N.; Diker, I. Y.; Ozuynuk, A. S.
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THE ROLE OF LIPOPROTEIN METABOLISM AND INFLAMMATORY GENE POLYMORPHIMS ON THE CORONARY ARTERY DISEASE WITH TYPE 2 DIABETES MELLITUS
err2018-08-01
err0
PREAI
errCoban, N.; Ozuynuk, A. S.; Erkan, A. F.; Ekici, B.; Vurgun, E.; Erginel-unaltuna, N.; Diker, I. Y.
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THE ROLE OF LIPID, SEX HORMONE AND INFLAMMATION PATHWAY GENES POLYMORPHIMS ON CORONARY ARTERY DISEASE IN TURKS
err2018-08-01
err0
PREAI
errOzuynuk, A. S.; Coban, N.; Erkan, A. F.; Ekici, B.; Vurgun, E.; Erginel-Unaltuna, N.; Diker, I. Y.
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Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey
err2018-03-01
err10
PREAI
errKessler, Christoph; Atasu, Burcu; Hanagasi, Hasmet; Simon-Sanchez, Javier; Hauser, Ann-Kathrin; Pak, Meltem; Bilgic, Basar; Erginel-Unaltuna, Nihan; Gurvit, Hakan; Gasser, Thomas; Lohmann, Ebba
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Mutations in TYROBP are not a common cause of dementia in a Turkish cohort
err2017-10-01
err8
errOAAI
errDarwent, Lee; Carmona, Susana; Lohmann, Ebba; Guven, Gamze; Kun-Rodrigues, Celia; Bilgic, Basar; Hanagasi, Hasmet; Gurvit, Hakan; Erginel-Unaltuna, Nihan; Pak, Meltem; Hardy, John; Singleton, Andrew; Bras, Jose; Guerreiro, Rita
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THE ROLE OF CYP19A1, ESR1 AND MIF GENES POLYMORPHIMS ON THE ANGIOGRAPHIC SEVERITY AND THE EXTENT OF ATHEROSCLEROTIC CORONARY ARTERY DISEASE
err2017-08-01
err0
PREAI
errCoban, Neslihan; Kaya, Aysem; Erkan, Aycan Fahri; Guclu-Geyik, Filiz; Ekici, Berkay; Ademoglu, Evin; Diker, Irem Yagmur; Can, Gunay; Erginel-Unaltuna, Nihan
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THE EXPRESSION PROFILES OF THE CANDIDATE MIRNAS AND THEIR TARGETS IN POST-MORTEM ADVANCED ATHEROSCLEROSIS
err2017-08-01
err0
PREAI
errBayrak, Evrim Komurcu; Geyik, Filiz Guclu; Cavlak, Mehmet; Demirel, Husrev; Erginel, Turgay; Unaltuna, Nihan Erginel
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Identification of potential target genes of ROR-alpha in THP1 and HUVEC cell lines
err2017-04-01
err9
PREAI
errGulec, Cagri; Coban, Neslihan; Ozsait-Selcuk, Bilge; Sirma-Ekmekci, Sema; Yildirim, Oziem; Erginel-Unaltuna, Nihan
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CYP19A1, MIF and ABCA1 genes are targets of the RORα in monocyte and endothelial cells
err2017-01-17
err19
PREAI
errCoban, Neslihan; Gulec, Cagri; Ozsait-Selcuk, Bilge; Erginel-Unaltuna, Nihan
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Loss of VPS1 3C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
err2016-03-01
err321
errOAAI
errLesage, Suzanne; Drouet, Valerie; Majounie, Elisa; Deramecourt, Vincent; Jacoupy, Maxime; Nicolas, Aude; Cormier-Dequaire, Florence; Hassoun, Sidi Mohamed; Pujol, Claire; Ciura, Sorana; Erpapazoglou, Zoi; Usenko, Tatiana; Maurage, Claude-Alain; Sahbatou, Mourad; Liebau, Stefan; Ding, Jinhui; Bilgic, Basar; Emre, Murat; Erginel-Unaltuna, Nihan; Guven, Gamze; Tison, Francois; Tranchant, Christine; Vidailhet, Marie; Corvol, Jean-Christophe; Krack, Paul; Leutenegger, Anne-Louise; Nalls, Michael A.; Hernandez, Dena G.; Heutink, Peter; Gibbs, J. Raphael; Hardy, John; Wood, Nicholas W.; Gasser, Thomas; Durr, Alexandra; Deleuze, Jean-Francois; Tazir, Meriem; Destee, Alain; Lohmann, Ebba; Kabashi, Edor; Singleton, Andrew; Corti, Olga; Brice, Alexis
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A new F-box protein 7 gene mutation causing typical Parkinson's disease
err2015-05-23
err52
PREAI
errLohmann, Ebba; Coquel, Anne-Sophie; Honore, Aurelie; Gurvit, Hakan; Hanagasi, Hasmet; Emre, Murat; Leutenegger, Anne L.; Drouet, Valerie; Sahbatou, Mourad; Guven, Gamze; Erginel-Unaltuna, Nihan; Deleuze, Jean-Francois; Lesage, Suzanne; Brice, Alexis
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Prevalence of Prader-Willi Syndrome among Infants with Hypotonia
err2014-05-01
err18
PREAI
errTuysuz, Beyhan; Kartal, Nuray; Erener-Ercan, Tugba; Guclu-Geyik, Filiz; Vural, Mehmet; Perk, Yildiz; Ercal, Derya; Erginel-Unaltuna, Nihan
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Gender-specific associations of the APOA1-75G > A polymorphism with several metabolic syndrome components in Turkish adults
err2014-04-01
err21
PREAI
errCoban, Neslihan; Onat, Altan; Guclu-Geyik, Filiz; Komurcu-Bayrak, Evrim; Can, Gunay; Erginel-Unaltuna, Nihan
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