Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 502 Records) |
Query Trace: CYP1B1[original query] |
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Biological and Clinical Implications of TNF-? Promoter and CYP1B1 Gene Variations in Coronary Artery Disease Susceptibility. Cardiovascular & hematological disorders drug targets 2021 12 21 (4): 266-277. Mir Rashid, Elfaki Imadeldin, Jha Chandan K, Javid Jamsheed, Babakr Abdullatif T, Banu Shaheena, Mir Mohammad M, Jamwal Dheeraj, Khullar Naina, Alzahrani Khalid J, Chahal Sukh M |
Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran. Journal of ophthalmic & vision research 0 16 (4): 574-581. Heshmati Ali, Taghizadeh Peyman, Ahmadieh Hamid, Yaseri Mehdi, Suri Fatemeh, Alizadeh Mahsa, Dadashzadeh Marjan, Khatami Hajar, Navi Monireh Moradkhah, Zamanparvar Parisa, Behboudi Hassan, Elahi Ela |
Effects of gene polymorphisms of CYP1A1, CYP1B1, EPHX1, NQO1, and NAT2 on urinary 1-nitropyrene metabolite concentrations. Heliyon 2022 8 8 (8): e10120. Yun Jung-Kuk, Ochirpurev Bolormaa, Eom Sang-Yong, Toriba Akira, Kim Yong-Dae, Kim He |
Identification by whole-exome sequencing of new single-nucleotide polymorphisms associated with molar-incisor hypomineralisation among the Lebanese population. European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry 2022 Aug . Elzein R, Abdel-Sater F, Mehawej C, Jalkh N, Ayoub F, Chouery |
Pharmacogenetics of taxane-induced neurotoxicity in breast cancer: Systematic review and meta-analysis. Clinical and translational science 2022 Jul . Guijosa Alberto, Freyria Ana, Espinosa-Fernandez Jose Rodrigo, Estrada-Mena Francisco J, Armenta-Quiroga Ana Sofía, Ortega-Treviño Maria Fernanda, Catalán Rodrigo, Antonio-Aguirre Bani, Villarreal-Garza Cynthia, Perez-Ortiz Andric |
Metal exposure and breast cancer among Northern Mexican women: assessment of genetic susceptibility. Environmental science and pollution research international 2022 Jul . Gamboa-Loira Brenda, Mérida-Ortega Ángel, Rothenberg Stephen J, Cebrián Mariano E, López-Carrillo Lizbe |
Urinary concentration of endocrine-disrupting phthalates and breast cancer risk in Indian women: A case-control study with a focus on mutations in phthalate-responsive genes. Cancer epidemiology 2022 6 79 102188. Mukherjee Das Ankan, Gogia Ajay, Garg Manoj, Elaiyaraja Arun, Arambam Priyadarshini, Mathur Sandeep, Babu-Rajendran Ramaswamy, Deo S V S, Kumar Lalit, Das Bhudev C, Janardhanan Raj |
Clinical Significance of Gene Mutations and Polymorphic Variants and their Association with Prostate Cancer Risk in Polish Men. Cancer control : journal of the Moffitt Cancer Center 2022 5 29 10732748211062342. Heise Marta, Jarzemski Piotr, Nowak Dagmara, B?k Aneta, Junkiert-Czarnecka Anna, Pilarska-Deltow Maria, Borysiak Maciej, Pilarska Beata, Haus Ol |
First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients. Clinical genetics 2022 2 101 (5-6): 494-506. Chesneau Bertrand, Aubert-Mucca Marion, Fremont Félix, Pechmeja Jacmine, Soler Vincent, Isidor Bertrand, Nizon Mathilde, Dollfus Hélène, Kaplan Josseline, Fares-Taie Lucas, Rozet Jean-Michel, Busa Tiffany, Lacombe Didier, Naudion Sophie, Amiel Jeanne, Rio Marlène, Attie-Bitach Tania, Lesage Cécile, Thouvenin Dominique, Odent Sylvie, Morel Godelieve, Vincent-Delorme Catherine, Boute Odile, Vanlerberghe Clémence, Dieux Anne, Boussion Simon, Faivre Laurence, Pinson Lucile, Laffargue Fanny, Le Guyader Gwenaël, Le Meur Guylène, Prieur Fabienne, Lambert Victor, Laudier Beatrice, Cottereau Edouard, Ayuso Carmen, Corton-Pérez Marta, Bouneau Laurence, Le Caignec Cédric, Gaston Véronique, Jeanton-Scaramouche Claire, Dupin-Deguine Delphine, Calvas Patrick, Chassaing Nicolas, Plaisancié Jul |
Identification of sex-specific genetic associations in response to opioid analgesics in a White, non-Hispanic cohort from Southeast Minnesota. The pharmacogenomics journal 2022 Jan . Lopes Guilherme S, Lopes Jaime L, Bielinski Suzette J, Armasu Sebastian M, Zhu Ye, Cavanaugh Dana C, Moyer Ann M, Jacobson Debra J, Wang Liwei, Jiang Ruoxiang, St Sauver Jennifer L, Larson Nicholas |
Estrogen-DNA Adducts and Breast Cancer Risk in Premenopausal Asian Women. Cancer prevention research (Philadelphia, Pa.) 2022 12 . Lin Ching-Hung, Zahid Muhammad, Kuo Wen-Hung, Hu Fu-Chang, Wang Ming-Yang, Chen I-Chun, Beseler Cheryl L, Mondal Bodhisattwa, Lu Yen-Shen, Rogan Eleanor G, Cheng Ann-L |
Genotype-phenotype association of PITX2 and FOXC1 in Axenfeld-Rieger syndrome. Experimental eye research 2022 11 226 109307. Zhou Lin, Wang Xiaoli, An Jingqi, Zhang Yao, He Mengxia, Tang |
Passive smoking and insomnia in rural Chinese nonsmoking housewives: An environmental and genetic perspective. Environment international 2022 Oct 170 107569. Jin Ming, Chen Huiting, Na Jigen, An Hang, Li Zhiwen, Li N |
Exome-based mutation screening in South African children with primary congenital glaucoma. Eye (London, England) 2022 Jan . Carstens Nadia, Goolam Saadiah, Hulley Michaella, Brandenburg Jean-Tristan, Ramsay Michele, Williams Susan Eileen Isabel |
Neonatal-Onset Congenital Ectropion Uveae May Be Caused by a Distinct CYP1B1 Pathologic Variant. American journal of ophthalmology 2022 1 239 54-65. Kaushik Sushmita, Choudhary Sandeep, Kaur Anupriya, Srivastava Priyanka, Pokharel Bikrant, Akella Madhuri, Pandav Surinder Sin |
DNA Repair and Replication-Related Gene Signature Based on Tumor Mutation Burden Reveals Prognostic and Immunotherapy Response in Gastric Cancer. Journal of oncology 2022 1 2022 6469523. Zhang Lei, Hu Dahai, Huangfu Shuchen, Zhou Jiaxin, Wang Wei, Liu Shijin, Tang Hui, Pan Jinghua, Pan Yunlo |
First Results from the Prospective German Registry for Childhood Glaucoma: Phenotype-Genotype Association. Journal of clinical medicine 2022 1 11 (1): . Stingl Julia V, Diederich Stefan, Diel Heidi, Schuster Alexander K, Wagner Felix M, Chronopoulos Panagiotis, Aghayeva Fidan, Grehn Franz, Winter Jennifer, Schweiger Susann, Hoffmann Esther |
Mutational analysis of CYP1B1 (rs56010818) variant in primary open angle glaucoma (POAG) affected patients of Pakistan. Saudi journal of biological sciences 2022 1 29 (1): 96-101. Narsani Ashok Kumar, Waryah Ali Muhammad, Rafiq Muhammad, Shaikh Hina, Naqvi Syed Habib Ahmed, Kumar Raveet, Kumar Paw |
Genotyping of the rs1800440 Polymorphism in CYP1B1 Gene and the rs9258883 Polymorphism in HLA-B Gene in a Spanish Cohort of 223 Patients with Frontal Fibrosing Alopecia. Acta dermato-venereologica 2023 9 103 adv9604. David Saceda-Corralo, Daniel Ortega-Quijano, Gloria Muñoz-Martín, Óscar M Moreno-Arrones, Cristina Pindado-Ortega, Tuntas Rayinda, Ana Melián-Olivera, Carlos Azcárraga-Llobet, Patricia Burgos-Blasco, María Elena Castañeda-Bermúdez, Francisco J Del Castillo, Sergio Vañó-Galv |
Copy number variations of cytochrome P450 genes in Kinh Vietnamese. Asian biomedicine : research, reviews and news 2023 9 17 (2): 84-92. Nhung Phuong Vu, Ton Dang Nguyen, Binh Huy Nguyen, Duong Thuy Nguyen, Hai Van Nong, Ha Hai Nguy |
Functional variant rs10175368 which affects the expression of CYP1B1 plays a protective role against breast cancer in a Chinese Han population. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 2023 4 . Liu Jiarui, Zhang Lijia, Tang Mingwen, Chen Xinyu, Yang Caiyun, Li Yong, Feng Jin, Deng Yan, Wang Xin, Zhang |
Investigation of mutational spectrum in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma. Pakistan journal of medical sciences 2023 3 39 (2): 409-416. Zahid Tazeen, Khan Muhammad Umer, Zulfiqar Aymn, Jawad Fatima, Saleem Anosh, Khan Ahmad Ra |
Corrigendum: Meta-analysis of CYP1B1 gene mutations in primary congenital glaucoma patients. European journal of ophthalmology 2023 2 11206721231156301. Authors are not available |
Exome Sequencing Reveals SLC4A11 Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma. Genes 2023 2 14 (2): . Yousaf Khazeema, Naz Sadaf, Mushtaq Asma, Wohler Elizabeth, Sobreira Nara, Ho Bo-Man, Chen Li-Jia, Chu Wai-Kit, Bashir Rashee |
Retracted: Medical Data Analysis of CYP1B1 Gene Polymorphism and Clinical Prognosis of Minimally Invasive Surgery for Lung Cancer. BioMed research international 2023 12 2023 9819417. BioMed Research Internation |
Evaluation of Comt2, Comt3, Cyp1b1, and Esr1 gene polymorphisms as risk factor for endometrial polyp. Women & health 2023 11 1-10. Marcos Tcherniakovsky, Emerson de Oliveira, Marina Martinelli Sonnenfeld, Marta M Arcoverde Cavalcanti Meniconi, Marília Franco de Oliveira, Isabella Tcherniakovsky, Thomas Moscovitz, Milton Wajman, Rogers Camargo Mariano da Silva, César Eduardo Fernand |
Systematic evaluation of clinical efficacy of CYP1B1 gene polymorphism in EGFR mutant non-small cell lung cancer observed by medical image. Open life sciences 2023 10 18 (1): 20220688. Shaofeng Zhang, Danqing Li, Xia H |
Wood cookstove use is associated with gastric cancer in Central America and mediated by host genetics. Scientific reports 2023 10 13 (1): 16515. Samara B Rifkin, Anna K Miller, Eleazar E Montalvan-Sanchez, Dalton A Norwood, Enrique Martinez, Tim Waterboer, T Mark Beasley, Ricardo L Dominguez, Scott M Williams, Douglas R Morg |
Clinical role of CYP1B1 gene polymorphism in prediction of postoperative chemotherapy efficacy in NSCLC based on individualized health model. Open life sciences 2023 10 18 (1): 20220705. Bo Liu, Shaofeng Zhang, Chunyan Liu, Xia H |
CYP1B1 Genetic Variants (rs10916 and rs2855658) Are Associated with Increased Risk of Ischemic Stroke in Chinese Han Population. Cerebrovascular diseases (Basel, Switzerland) 2023 1 1-13. Zhang Fan, Fu Chuanyi, Deng Yidong, Zhang Mao, Peng Hao, Li Wenan, Zhong Jian, Zhou Qing, Huang Li, Xiao Shuli, Zhao Jianno |
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- Page last updated:Apr 22, 2024
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