Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: PNKP[original query] |
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Polynucleotide kinase 3' phosphatase variant, dietary variables and risk of adenoma recurrence in the Polyp Prevention Trial. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 2008 Jun 17 (3): 287-90. Murphy Gwen, Sansbury Leah S, Bergen Andrew W, Wang Zhuoqiao, Schatzkin Arthur, Lehman Teresa, Kalidindi Aravind, Modali Rama, Lanza Elai |
Increased risk of lung cancer associated with a functionally impaired polymorphic variant of the human DNA glycosylase NEIL2. DNA repair 2012 Jun 11 (6): 570-8. Dey Sanjib, Maiti Amit K, Hegde Muralidhar L, Hegde Pavana M, Boldogh Istvan, Sarkar Partha S, Abdel-Rahman Sherif Z, Sarker Altaf H, Hang Bo, Xie Jingwu, Tomkinson Alan E, Zhou Mian, Shen Binghui, Wang Guanghai, Wu Chen, Yu Dianke, Lin Dongxin, Cardenas Victor, Hazra Tapas |
Domain analysis of PNKP-XRCC1 interactions: Influence of genetic variants of XRCC1. The Journal of biological chemistry 2018 11 294 (2): 520-530. Mani Rajam S, Mermershtain Inbal, Abdou Ismail, Fanta Mesfin, Hendzel Michael J, Glover J N Mark, Weinfeld Micha |
Ataxia with Oculomotor Apraxia Type 4 with PNKP Common "Portuguese" and Novel Mutations in Two Belarusian Families. Journal of pediatric genetics 2019 5 8 (2): 58-62. Rudenskaya Galina E, Marakhonov Andrey V, Shchagina Olga A, Lozier Ekaterina R, Dadali Elena L, Akimova Irina A, Petrova Nika V, Konovalov Fedor |
Compound Heterozygous Mutations in PNKP Gene in an Iranian Child with Microcephaly, Seizures, and Developmental Delay. Fetal and pediatric pathology 2019 11 40 (2): 174-180. Bitarafan Fatemeh, Khodaeian Mehrnoosh, Almadani Navid, Kalhor Alireza, Sardehaei Elham Amjadi, Garshasbi Maso |
The Phenotypic Spectrum of PNKP-Associated Disease and the Absence of Immunodeficiency and Cancer Predisposition in a Dutch Cohort. Pediatric neurology 2020 9 113 26-32. Garrelfs Mark R, Takada Sanami, Kamsteeg Erik-Jan, Pegge Sjoert, Mancini Grazia, Engelen Marc, van de Warrenburg Bart, Rennings Alexander, van Gaalen Judith, Peters Ivo, Weemaes Corry, van der Burg Mirjam, Willemsen Michèl |
Clinical and Genetic Characterization of Brazilian Patients with Ataxia and Oculomotor Apraxia. Movement disorders : official journal of the Movement Disorder Society 2022 4 37 (6): 1309-1316. da Costa Sophia Caldas Gonzaga, de Rezende-Filho Flávio C, de Freitas Júlian Leticia, de Assis Pereira Matos Paula Camila Alves, Della-Ripa Bruno, França Marcondes Cavalcante, Marques Wilson, Santos Mariana, Cronemberger Igor Vasconcelos Barros, Vale Thiago Cardoso, Kok Fernando, Alonso Isabel, Pedroso José Luiz, Barsottini Orlando G |
HLA - matched related donor hematopoietic stem cell transplantation in a patient with polynucleotide kinase 3-phosphatase mutation developed acute myeloid leukemia. Pediatric transplantation 2022 2 26 (4): e14255. Bayram Nihan, Yaman Yontem, Elli Murat, Ozdilli Kursat, Nepesov Serdar, Dogan Mehmet Sait, Ayaz Akif, Anak Se |
Antioxidant enzyme and DNA base repair genetic risk scores' associations with systemic oxidative stress biomarker in pooled cross-sectional studies. Frontiers in aging 2023 5 4 1000166. Ziling Mao, Abigail L H Gray, Bharat Thyagarajan, Roberd M Bosti |
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- Page last updated:Apr 16, 2024
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