CAT c.1167C>T ;(p.D389=)

Variant ID: 11-34482908-C-T

NM_001752.3(CAT):c.1167C>T;(p.D389=)

This variant was identified in 65 publications

View GRCh38 version.




Publications:


Evaluation of CAT Variants A-89T, C389T, and C419T in Patients with Vitiligo in the Saudi Population.

Medicina (Kaunas, Lithuania)
Saif, Ghada A Bin GAB; Alshammary, Amal F AF; Ali Khan, Imran I
Publication Date: 2023-04-04

Variant appearance in text: rs769217
PubMed Link: 37109666
Variant Present in the following documents:
  • Main text
  • medicina-59-00708.pdf
View BVdb publication page



Comprehensive proteogenomic characterization of early duodenal cancer reveals the carcinogenesis tracks of different subtypes.

Nature Communications
Li, Lingling L; Jiang, Dongxian D; Liu, Hui H; Guo, Chunmei C; Zhao, Rui R; Zhang, Qiao Q; Xu, Chen C; Qin, Zhaoyu Z; Feng, Jinwen J; Liu, Yang Y; Wang, Haixing H; Chen, Weijie W; Zhang, Xue X; Li, Bin B; Bai, Lin L; Tian, Sha S; Tan, Subei S; Yu, Zixiang Z; Chen, Lingli L; Huang, Jie J; Zhao, Jian-Yuan JY; Hou, Yingyong Y; Ding, Chen C
Publication Date: 2023-03-29

Variant appearance in text: rs769217
PubMed Link: 36991000
Variant Present in the following documents:
  • 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3
View BVdb publication page



Association of variations in the CAT and prognosis in lung cancer patients with platinum-based chemotherapy.

Frontiers In Pharmacology
Liu, Jia-Si JS; Liu, Jun-Yan JY; Xiao, Qi Q; Li, Xiang-Ping XP; Chen, Juan J; Liu, Zhao-Qian ZQ
Publication Date: 2023

Variant appearance in text: rs769217
PubMed Link: 36969849
Variant Present in the following documents:
  • Main text
  • fphar-14-1119837.pdf
View BVdb publication page



Molecular Genetics of Abnormal Redox Homeostasis in Type 2 Diabetes Mellitus.

International Journal Of Molecular Sciences
Azarova, Iuliia I; Polonikov, Alexey A; Klyosova, Elena E
Publication Date: 2023-03-01

Variant appearance in text: rs769217
PubMed Link: 36902173
Variant Present in the following documents:
  • Main text
  • ijms-24-04738.pdf
View BVdb publication page



The Genetic Diversity and Dysfunctionality of Catalase Associated with a Worse Outcome in Crohn's Disease.

International Journal Of Molecular Sciences
Iborra, Marisa M; Moret, Inés I; Busó, Enrique E; García-Giménez, José Luis JL; Ricart, Elena E; Gisbert, Javier P JP; Cabré, Eduard E; Esteve, Maria M; Márquez-Mosquera, Lucía L; García-Planella, Esther E; Guardiola, Jordi J; Pallardó, Federico V FV; Serena, Carolina C; Algaba-Chueca, Francisco F; Domenech, Eugeni E; Nos, Pilar P; Beltrán, Belén B
Publication Date: 2022-12-14

Variant appearance in text: rs769217
PubMed Link: 36555526
Variant Present in the following documents:
  • Main text
  • ijms-23-15881.pdf
View BVdb publication page



Pharmacogenetics Role of Genetic Variants in Immune-Related Factors: A Systematic Review Focusing on mCRC.

Pharmaceutics
Scarabel, Lucia L; Bignucolo, Alessia A; Toffoli, Giuseppe G; Cecchin, Erika E; De Mattia, Elena E
Publication Date: 2022-11-15

Variant appearance in text: rs769217
PubMed Link: 36432658
Variant Present in the following documents:
  • Main text
  • pharmaceutics-14-02468.pdf
View BVdb publication page



Beneficial effects of mifepristone treatment in breast cancer patients selected by the progesterone receptor isoform ratio: Results from the MIPRA trial.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Elía, Andrés A; Saldain, Leo L; Vanzulli, Silvia I SI; Helguero, Luisa A LA; Lamb, Caroline A CA; Fabris, Victoria V; Pataccini, Gabriela G; Martínez-Vazquez, Paula P; Burruchaga, Javier J; Caillet-Bois, Ines I; Spengler, Eunice E; Acosta Haab, Gabriela G; Liguori, Marcos M; Castets, Alejandra A; Lovisi, Silvia S; Abascal, María F MF; Novaro, Virginia V; Sánchez, Jana J; Muñoz, Javier J; Belizán, Jose M JM; Abba, Martín C MC; Gass, Hugo H; Rojas, Paola P; Lanari, Claudia C
Publication Date: 2022-10-21

Variant appearance in text: rs769217
PubMed Link: 36269797
Variant Present in the following documents:
  • ccr-22-2060_supplementary_table_s5_suppts5.xlsx, sheet 1
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs769217
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation
Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-09-08

Variant appearance in text: rs769217
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM3_ESM.xlsx, sheet 2
  • 41439_2022_208_MOESM5_ESM.xlsx, sheet 2
View BVdb publication page



A comprehensive meta-analysis and prioritization study to identify vitiligo associated coding and non-coding SNV candidates using web-based bioinformatics tools.

Scientific Reports
Dutta, Tithi T; Mitra, Sayantan S; Saha, Arpan A; Ganguly, Kausik K; Pyne, Tushar T; Sengupta, Mainak M
Publication Date: 2022-08-25

Variant appearance in text: rs769217
PubMed Link: 36008553
Variant Present in the following documents:
  • Main text
  • 41598_2022_Article_18766.pdf
View BVdb publication page



The Role of Genetic Variants in the Susceptibility of Noise-Induced Hearing Loss.

Frontiers In Cellular Neuroscience
Chen, Xue-Min XM; Xue, Xin-Miao XM; Yu, Ning N; Guo, Wei-Wei WW; Yuan, Shuo-Long SL; Jiang, Qing-Qing QQ; Yang, Shi-Ming SM
Publication Date: 2022

Variant appearance in text: rs769217
PubMed Link: 35903368
Variant Present in the following documents:
  • Main text
  • fncel-16-946206.pdf
View BVdb publication page



Association Between Antioxidant Nutrients, Oxidative Stress-Related Gene Polymorphism and Skeletal Fluorosis in Guizhou, China.

Frontiers In Public Health
Tao, Na N; Li, Lianhong L; Chen, Qing Q; Sun, Zhongming Z; Yang, Qinglin Q; Cao, Dafang D; Zhao, Xun X; Zeng, Fangfang F; Liu, Jun J
Publication Date: 2022

Variant appearance in text: rs769217
PubMed Link: 35646794
Variant Present in the following documents:
  • Main text
  • fpubh-10-849173.pdf
View BVdb publication page



Asian Race and Primary Open-Angle Glaucoma: Where Do We Stand?

Journal Of Clinical Medicine
Belamkar, Aditya A; Harris, Alon A; Oddone, Francesco F; Verticchio Vercellin, Alice A; Fabczak-Kubicka, Anna A; Siesky, Brent B
Publication Date: 2022-04-28

Variant appearance in text: rs769217
PubMed Link: 35566612
Variant Present in the following documents:
  • jcm-11-02486.pdf
View BVdb publication page



A novel missense variant in CEACAM16 gene causes autosomal dominant nonsyndromic hearing loss.

Annals Of Human Genetics
Zhang, Dejun D; Wu, Jie J; Yuan, Yongyi Y; Li, Xiaohong X; Gao, Xue X; Han, Mingyu M; Gao, Song S; Huang, Shasha S; Dai, Pu P
Publication Date: 2022-07

Variant appearance in text: rs769217
PubMed Link: 35292975
Variant Present in the following documents:
  • AHG-86-207-s002.xlsx, sheet 1
View BVdb publication page



Genetic Polymorphisms of MnSOD Modify the Impacts of Environmental Melamine on Oxidative Stress and Early Kidney Injury in Calcium Urolithiasis Patients.

Antioxidants (Basel, Switzerland)
Liu, Chia-Chu CC; Wu, Chia-Fang CF; Lee, Yung-Chin YC; Huang, Tsung-Yi TY; Huang, Shih-Ting ST; Wang, Hsun-Shuan HS; Jhan, Jhen-Hao JH; Huang, Shu-Pin SP; Li, Ching-Chia CC; Juan, Yung-Shun YS; Hsieh, Tusty-Jiuan TJ; Tsai, Yi-Chun YC; Chen, Chu-Chih CC; Wu, Ming-Tsang MT
Publication Date: 2022-01-13

Variant appearance in text: rs769217
PubMed Link: 35052656
Variant Present in the following documents:
  • Main text
  • antioxidants-11-00152.pdf
View BVdb publication page



Genetic Polymorphisms of MnSOD Modify the Impacts of Environmental Melamine on Oxidative Stress and Early Kidney Injury in Calcium Urolithiasis Patients.

Antioxidants (Basel, Switzerland)
Liu, Chia-Chu CC; Wu, Chia-Fang CF; Lee, Yung-Chin YC; Huang, Tsung-Yi TY; Huang, Shih-Ting ST; Wang, Hsun-Shuan HS; Jhan, Jhen-Hao JH; Huang, Shu-Pin SP; Li, Ching-Chia CC; Juan, Yung-Shun YS; Hsieh, Tusty-Jiuan TJ; Tsai, Yi-Chun YC; Chen, Chu-Chih CC; Wu, Ming-Tsang MT
Publication Date: 2022-01-13

Variant appearance in text: rs769217
PubMed Link: 35052656
Variant Present in the following documents:
  • Main text
  • antioxidants-11-00152.pdf
View BVdb publication page



Genetic Susceptibility to Acute Kidney Injury.

Journal Of Clinical Medicine
Ortega-Loubon, Christian C; Martínez-Paz, Pedro P; García-Morán, Emilio E; Tamayo-Velasco, Álvaro Á; López-Hernández, Francisco J FJ; Jorge-Monjas, Pablo P; Tamayo, Eduardo E
Publication Date: 2021-07-08

Variant appearance in text: rs769217
PubMed Link: 34300206
Variant Present in the following documents:
  • Main text
  • jcm-10-03039.pdf
View BVdb publication page



Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes.

Frontiers In Genetics
Feng, Wei-Xing WX; Zhuo, Xiu-Wei XW; Liu, Zhi-Mei ZM; Li, Jiu-Wei JW; Zhang, Wei-Hua WH; Wu, Yun Y; Han, Tong-Li TL; Fang, Fang F
Publication Date: 2021

Variant appearance in text: rs769217
PubMed Link: 34054912
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Association of Genetic Polymorphisms in Oxidative Stress and Inflammation Pathways with Glaucoma Risk and Phenotype.

Journal Of Clinical Medicine
Atanasovska Velkovska, Makedonka M; Goričar, Katja K; Blagus, Tanja T; Dolžan, Vita V; Cvenkel, Barbara B
Publication Date: 2021-03-09

Variant appearance in text: rs769217
PubMed Link: 33803434
Variant Present in the following documents:
  • Main text
  • jcm-10-01148.pdf
View BVdb publication page



Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology
Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA
Publication Date: 2021

Variant appearance in text: rs769217
PubMed Link: 33791233
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Integrated genetic and metabolic landscapes predict vulnerabilities of temozolomide resistant glioblastoma cells.

Npj Systems Biology And Applications
Immanuel, Selva Rupa Christinal SRC; Ghanate, Avinash D AD; Parmar, Dharmeshkumar S DS; Yadav, Ritu R; Uthup, Riya R; Panchagnula, Venkateswarlu V; Raghunathan, Anu A
Publication Date: 2021-01-08

Variant appearance in text: rs769217
PubMed Link: 33420045
Variant Present in the following documents:
  • 41540_2020_161_MOESM3_ESM.xlsx, sheet 3
  • 41540_2020_161_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



Hsp70/Bmi1-FoxO1-SOD Signaling Pathway Contributes to the Protective Effect of Sound Conditioning against Acute Acoustic Trauma in a Rat Model.

Neural Plasticity
Zhu, Guoxia G; Wu, Yongxiang Y; Qiu, Yang Y; Tian, Keyong K; Mi, Wenjuan W; Liu, Xinqin X; Chen, Yuanyuan Y; Jia, Jinwen J; Luo, Jiasheng J; Lu, Lianjun L; Qiu, Jianhua J
Publication Date: 2020

Variant appearance in text: rs769217
PubMed Link: 33082778
Variant Present in the following documents:
  • Main text
  • NP2020-8823785.pdf
View BVdb publication page



Identification of a nonsense mutation in TNNI3K associated with cardiac conduction disease.

Journal Of Clinical Laboratory Analysis
Liu, Jiang J; Liu, Da D; Li, Muzheng M; Wu, Keke K; Liu, Na N; Zhao, Chenyu C; Shi, Xiaoliu X; Liu, Qiming Q
Publication Date: 2020-09

Variant appearance in text: rs769217
PubMed Link: 32529721
Variant Present in the following documents:
  • JCLA-34-e23418-s003.xls, sheet 1
View BVdb publication page



Prelingual Sensorineural Hearing Loss Caused by a Novel GJB2 Dominant Mutation in a Chinese Family.

Biomed Research International
Huang, Shasha S; Gao, Xue X; Wang, Yufeng Y; Kang, Dongyang D; Zhang, Xin X; Yang, Suyan S; Dai, Pu P
Publication Date: 2020

Variant appearance in text: rs769217
PubMed Link: 32090102
Variant Present in the following documents:
  • 6370386.f1.xlsx, sheet 2
View BVdb publication page



Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders
Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M
Publication Date: 2020-02-11

Variant appearance in text: rs769217
PubMed Link: 32046637
Variant Present in the following documents:
  • 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



A Polymorphism in the Catalase Gene Promoter Confers Protection against Severe RSV Bronchiolitis.

Viruses
Chambliss, Jeffrey M JM; Ansar, Maria M; Kelley, John P JP; Spratt, Heidi H; Garofalo, Roberto P RP; Casola, Antonella A
Publication Date: 2020-01-03

Variant appearance in text: rs769217
PubMed Link: 31947722
Variant Present in the following documents:
  • Main text
  • viruses-12-00057.pdf
View BVdb publication page



NRF2: The key to tumor- and patient-dependent chemosensitivity in biliary tract cancer?

Ebiomedicine
Kiesslich, Tobias T; Mayr, Christian C; Neureiter, Daniel D
Publication Date: 2019-11

Variant appearance in text: rs769217
PubMed Link: 31648982
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports
Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA
Publication Date: 2019-10-09

Variant appearance in text: rs769217
PubMed Link: 31597922
Variant Present in the following documents:
  • 41598_2019_50891_MOESM5_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



Variants in oxidative stress-related genes affect the chemosensitivity through Nrf2-mediated signaling pathway in biliary tract cancer.

Ebiomedicine
Zhan, Ming M; Wang, Hui H; Xu, Sun-Wang SW; Yang, Lin-Hua LH; Chen, Wei W; Zhao, Shuang-Xia SX; Shen, Hui H; Liu, Qiang Q; Yang, Rui-Meng RM; Wang, Jian J
Publication Date: 2019-10

Variant appearance in text: rs769217
PubMed Link: 31590928
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Association of genetic polymorphisms in SOD2, SOD3, GPX3, and GSTT1 with hypertriglyceridemia and low HDL-C level in subjects with high risk of coronary artery disease.

Peerj
Decharatchakul, Nisa N; Settasatian, Chatri C; Settasatian, Nongnuch N; Komanasin, Nantarat N; Kukongviriyapan, Upa U; Intharaphet, Phongsak P; Senthong, Vichai V
Publication Date: 2019

Variant appearance in text: rs769217
PubMed Link: 31396447
Variant Present in the following documents:
  • peerj-07-7407.pdf
View BVdb publication page



Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.

Cell Death & Disease
Grassi, Ludovica L; Alfonsi, Romina R; Francescangeli, Federica F; Signore, Michele M; De Angelis, Maria Laura ML; Addario, Antonio A; Costantini, Manuela M; Flex, Elisabetta E; Ciolfi, Andrea A; Pizzi, Simone S; Bruselles, Alessandro A; Pallocca, Matteo M; Simone, Giuseppe G; Haoui, Mustapha M; Falchi, Mario M; Milella, Michele M; Sentinelli, Steno S; Di Matteo, Paola P; Stellacci, Emilia E; Gallucci, Michele M; Muto, Giovanni G; Tartaglia, Marco M; De Maria, Ruggero R; Bonci, Désirée D
Publication Date: 2019-02-27

Variant appearance in text: rs769217
PubMed Link: 30814510
Variant Present in the following documents:
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 3
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 2
View BVdb publication page



Integrative molecular profiling identifies a novel cluster of estrogen receptor-positive breast cancer in very young women.

Cancer Science
Park, Charny C; Yoon, Kyong-Ah KA; Kim, Jihyun J; Park, In Hae IH; Park, Soo Jin SJ; Kim, Min Kyeong MK; Jang, Wooyeong W; Cho, Soo Young SY; Park, Boyoung B; Kong, Sun-Young SY; Lee, Eun Sook ES
Publication Date: 2019-05

Variant appearance in text: rs769217
PubMed Link: 30811755
Variant Present in the following documents:
  • CAS-110-1760-s002.xlsx, sheet 2
View BVdb publication page



Genetic polymorphisms associated with reactive oxygen species and blood pressure regulation.

The Pharmacogenomics Journal
Cuevas, Santiago S; Villar, Van Anthony M VAM; Jose, Pedro A PA
Publication Date: 2019-08

Variant appearance in text: rs769217
PubMed Link: 30723314
Variant Present in the following documents:
  • Main text
  • nihms-1517349.pdf
View BVdb publication page



Identification of novel compound heterozygous SPG7 mutations-related hereditary spastic paraplegia in a Chinese family: a case report.

Bmc Neurology
Zhang, Xiaoqian X; Zhang, Lei L; Wu, Yanqing Y; Li, Gang G; Chen, Shengcai S; Xia, Yuanpeng Y; Li, Hongge H
Publication Date: 2018-11-29

Variant appearance in text: rs769217
PubMed Link: 30497413
Variant Present in the following documents:
  • 12883_2018_1199_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: rs769217
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
  • Table_7.xlsx, sheet 1
View BVdb publication page



A likely pathogenic variant putatively affecting splicing of PIGA identified in a multiple congenital anomalies hypotonia-seizures syndrome 2 (MCAHS2) family pedigree via whole-exome sequencing.

Molecular Genetics & Genomic Medicine
Yang, Junli J; Wang, Qiong Q; Zhuo, Qingcui Q; Tian, Huiling H; Li, Wen W; Luo, Fang F; Zhang, Jinghui J; Bi, Dan D; Peng, Jing J; Zhou, Dong D; Xin, Huawei H
Publication Date: 2018-09

Variant appearance in text: rs769217
PubMed Link: 29974678
Variant Present in the following documents:
  • MGG3-6-739-s002.xlsx, sheet 7
  • MGG3-6-739-s002.xlsx, sheet 4
  • MGG3-6-739-s002.xlsx, sheet 6
  • MGG3-6-739-s002.xlsx, sheet 3
View BVdb publication page



Association between single nucleotide polymorphisms in the antioxidant genes CAT, GR and SOD1, erythrocyte enzyme activities, dietary and life style factors and breast cancer risk in a Danish, prospective cohort study.

Oncotarget
Kopp, Tine Iskov TI; Vogel, Ulla U; Dragsted, Lars Ove LO; Tjonneland, Anne A; Ravn-Haren, Gitte G
Publication Date: 2017-09-08

Variant appearance in text: rs769217
PubMed Link: 28968965
Variant Present in the following documents:
  • Main text
  • oncotarget-08-62984.pdf
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs769217
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Analyses of antioxidant status and nucleotide alterations in genes encoding antioxidant enzymes in patients with benign and malignant thyroid disorders.

Peerj
Ramli, Nur Siti Fatimah NSF; Mat Junit, Sarni S; Leong, Ng Khoon NK; Razali, Nurhanani N; Jayapalan, Jaime Jacqueline JJ; Abdul Aziz, Azlina A
Publication Date: 2017

Variant appearance in text: rs769217
PubMed Link: 28584708
Variant Present in the following documents:
  • Main text
  • peerj-05-3365.pdf
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs769217
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
Publication Date: 2017-05-12

Variant appearance in text: rs769217
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Increase of urinary malondialdehyde level by bisphenol A exposure: a longitudinal panel study.

Environmental Health : A Global Access Science Source
Kim, Jin Hee JH; Hong, Yun-Chul YC
Publication Date: 2017-02-15

Variant appearance in text: rs769217
PubMed Link: 28202054
Variant Present in the following documents:
  • Main text
  • 12940_2017_Article_221.pdf
View BVdb publication page



Oxidative stress, a trigger of hepatitis C and B virus-induced liver carcinogenesis.

Oncotarget
Ivanov, Alexander V AV; Valuev-Elliston, Vladimir T VT; Tyurina, Daria A DA; Ivanova, Olga N ON; Kochetkov, Sergey N SN; Bartosch, Birke B; Isaguliants, Maria G MG
Publication Date: 2017-01-17

Variant appearance in text: rs769217
PubMed Link: 27965466
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations of air pollution exposure with blood pressure and heart rate variability are modified by oxidative stress genes: A repeated-measures panel among elderly urban residents.

Environmental Health : A Global Access Science Source
Kim, Kyoung-Nam KN; Kim, Jin Hee JH; Jung, Kweon K; Hong, Yun-Chul YC
Publication Date: 2016-03-25

Variant appearance in text: rs769217
PubMed Link: 27015811
Variant Present in the following documents:
  • Main text
View BVdb publication page



Control for stochastic sampling variation and qualitative sequencing error in next generation sequencing.

Biomolecular Detection And Quantification
Blomquist, Thomas T; Crawford, Erin L EL; Yeo, Jiyoun J; Zhang, Xiaolu X; Willey, James C JC
Publication Date: 2015-09-01

Variant appearance in text: rs769217
PubMed Link: 26693143
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page