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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 10 (of 10 Records)

Query Trace: Disease and NEIL1[original query]
Catalytically impaired hMYH and NEIL1 mutant proteins identified in patients with primary sclerosing cholangitis and cholangiocarcinoma.
Carcinogenesis 2009 Jul 30 (7): 1147-54.
Forsbring Monika, Vik Erik S, Dalhus Bjørn, Karlsen Tom H, Bergquist Annika, Schrumpf Erik, Bjørås Magnar, Boberg Kirsten M, Alseth Ingr
Prevalence of the DNA repair enzyme-NEIL1 gene mutation in patients with type 2 diabetes in the Turkish population.
Journal of endocrinological investigation 2012 Apr 35 (4): 401-6.
Salmanoglu M, Kucukardali Y, Kucukodaci Z, Fenercioglu A, Solmazgul E, Onem Y, Baloglu H, Ozata
Polymorphism of the DNA base excision repair genes in keratoconus.
International journal of molecular sciences 2014 15 (11): 19682-99.
Wojcik Katarzyna A, Synowiec Ewelina, Sobierajczyk Katarzyna, Izdebska Justyna, Blasiak Janusz, Szaflik Jerzy, Szaflik Jacek
Variation in DNA Base Excision Repair Genes in Fuchs Endothelial Corneal Dystrophy.
Medical science monitor : international medical journal of experimental and clinical research 2015 21 2809-27.
Wójcik Katarzyna A, Synowiec Ewelina, Polakowski Piotr, B?asiak Janusz, Szaflik Jerzy, Szaflik Jacek
Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease.
Arthritis & rheumatology (Hoboken, N.J.) 2015 Dec .
Ognenovski Mikhail, Renauer Paul, Gensterblum Elizabeth, Kötter Ina, Xenitidis Theodoros, Henes Jörg C, Casali Bruno, Salvarani Carlo, Direskeneli Haner, Kaufman Kenneth M, Sawalha Amr
Association between Single-Nucleotide Polymorphisms of the hOGG1,NEIL1,APEX1, FEN1,LIG1, and LIG3 Genes and Alzheimer's Disease Risk.
Neuropsychobiology 2016 73 (2): 98-107.
Kwiatkowski Dominik, Czarny Piotr, Toma Monika, Korycinska Anna, Sowinska Katarzyna, Galecki Piotr, Bachurska Agnieszka, Bielecka-Kowalska Anna, Szemraj Janusz, Maes Michael, Sliwinski Toma
Defective repair capacity of variant proteins of the DNA glycosylase NTHL1 for 5-hydroxyuracil, an oxidation product of cytosine.
Free radical biology & medicine 2018 12 131 264-273.
Shinmura Kazuya, Kato Hisami, Kawanishi Yuichi, Goto Masanori, Tao Hong, Yoshimura Katsuhiro, Nakamura Satoki, Misawa Kiyoshi, Sugimura Haruhi
Investigation of base excision repair gene variants in late-onset Alzheimer's disease.
PloS one 2019 14 (8): e0221362.
Ertuzun Tugce, Semerci Asli, Cakir Mehmet Emin, Ekmekcioglu Aysegul, Gok Mehmet Oguz, Soltys Daniela T, de Souza-Pinto Nadja C, Sezerman Ugur, Muftuoglu Melt
Deregulated DNA damage response network in Behcet's disease.
Clinical immunology (Orlando, Fla.) 2022 11 246 109189.
Vlachogiannis Nikolaos I, Ntouros Panagiotis A, Pappa Maria, Verrou Kleio-Maria, Arida Aikaterini, Souliotis Vassilis L, Sfikakis Petros
Single-Nucleotide Polymorphisms in Base-Excision Repair-Related Genes Involved in the Risk of an Occurrence of Non-Alcoholic Fatty Liver Disease.
International journal of molecular sciences 2023 7 24 (14): .
Sylwia Zió?kowska, Marcin Kosmalski, ?ukasz Ko?odziej, Aleksandra Jab?kowska, Janusz Zbigniew Szemraj, Tadeusz Pietras, Maciej Jab?kowski, Piotr Lech Czar
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