Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: CYP26A1[original query] |
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Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2. Birth defects research. Part A, Clinical and molecular teratology 2005 Nov 73 (11): 868-75. Deak Kristen L, Dickerson Margaret E, Linney Elwood, Enterline David S, George Timothy M, Melvin Elizabeth C, Graham Felicia L, Siegel Deborah G, Hammock Preston, Mehltretter Lorraine, Bassuk Alexander G, Kessler John A, Gilbert John R, Speer Marcy C, |
Evidence for a functional genetic polymorphism of the human retinoic acid-metabolizing enzyme CYP26A1, an enzyme that may be involved in spina bifida. Birth defects research. Part A, Clinical and molecular teratology 2006 Jun 76 (6): 491-8. Rat Emmanuel, Billaut-Laden Ingrid, Allorge Delphine, Lo-Guidice Jean-Marc, Tellier Marie, Cauffiez Christelle, Jonckheere Nicolas, van Seuningen Isabelle, Lhermitte Michel, Romano Antonio, Guéant Jean-Louis, Broly Fran |
Mutational screening of the CYP26A1 gene in patients with caudal regression syndrome. Birth defects research. Part A, Clinical and molecular teratology 2006 Feb 76 (2): 86-95. De Marco Patrizia, Merello Elisa, Mascelli Samantha, Raso Alessandro, Santamaria Andrea, Ottaviano Catherine, Calevo Maria Grazia, Cama Armando, Capra Valer |
Positive association between ALDH1A2 and schizophrenia in the Chinese population. Progress in neuro-psychopharmacology & biological psychiatry 2009 Nov 33 (8): 1491-5. Wan Chunling, Shi Yongyong, Zhao Xinzhi, Tang Wei, Zhang Ming, Ji Baohu, Zhu Hui, Xu Yifeng, Li Huafang, Feng Guoyin, He L |
A human ALDH1A2 gene variant is associated with increased newborn kidney size and serum retinoic acid. Kidney international 2010 Jul 78 (1): 96-102. El Kares Reyhan, Manolescu Daniel C, Lakhal-Chaieb Lajmi, Montpetit Alexandre, Zhang Zhao, Bhat Pangala V, Goodyer Pa |
Evaluation of genes involved in limb development, angiogenesis, and coagulation as risk factors for congenital limb deficiencies. American journal of medical genetics. Part A 2012 Oct 158A (10): 2463-72. Browne Marilyn L, Carter Tonia C, Kay Denise M, Kuehn Devon, Brody Lawrence C, Romitti Paul A, Liu Aiyi, Caggana Michele, Druschel Charlotte M, Mills James |
Comprehensive replication of the relationship between myopia-related genes and refractive errors in a large Japanese cohort. Investigative ophthalmology & visual science 2014 Nov 55 (11): 7343-54. Yoshikawa Munemitsu, Yamashiro Kenji, Miyake Masahiro, Oishi Maho, Akagi-Kurashige Yumiko, Kumagai Kyoko, Nakata Isao, Nakanishi Hideo, Oishi Akio, Gotoh Norimoto, Yamada Ryo, Matsuda Fumihiko, Yoshimura Nagahisa, |
Association study between novel CYP26 polymorphisms and the risk of betel quid-related malignant oral disorders. TheScientificWorldJournal 2015 2015 160185. Wu Shyh-Jong, Chen Yun-Ju, Shieh Tien-Yu, Chen Chun-Ming, Wang Yen-Yun, Lee Kun-Tsung, Lin Yueh-Ming, Chien Pei-Hsuan, Chen Ping- |
Retinoic Acid Modulates PTGDR Promoter Activity. Journal of investigational allergology & clinical immunology 2016 Apr 26 (4): . García-Sánchez A, Marcos-Vadillo E, Sanz C, Hernández-Hernández L, Cerutti-Müller G, Marqués-García F, Lorente F, Isidoro-García M, Dávila |
A novel de novo mutation in MYT1, the unique OAVS gene identified so far. European journal of human genetics : EJHG 2017 Jun . Berenguer Marie, Tingaud-Sequeira Angele, Colovati Mileny, Melaragno Maria I, Bragagnolo Silvia, Perez Ana B A, Arveiler Benoit, Lacombe Didier, Rooryck Caroli |
Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma.
Scientific reports 2018 Feb 8 (1): 3124. Gharahkhani Puya, Burdon Kathryn P, Cooke Bailey Jessica N, Hewitt Alex W, Law Matthew H, Pasquale Louis R, Kang Jae H, Haines Jonathan L, Souzeau Emmanuelle, Zhou Tiger, Siggs Owen M, Landers John, Awadalla Mona, Sharma Shiwani, Mills Richard A, Ridge Bronwyn, Lynn David, Casson Robert, Graham Stuart L, Goldberg Ivan, White Andrew, Healey Paul R, Grigg John, Lawlor Mitchell, Mitchell Paul, Ruddle Jonathan, Coote Michael, Walland Mark, Best Stephen, Vincent Andrea, Gale Jesse, RadfordSmith Graham, Whiteman David C, Montgomery Grant W, Martin Nicholas G, Mackey David A, Wiggs Janey L, MacGregor Stuart, Craig Jamie E, |
CYP26A1 Is a Novel Biomarker for Betel Quid-Related Oral and Pharyngeal Cancers. Diagnostics (Basel, Switzerland) 2020 11 10 (11): . Chen Ping-Ho, Chung Chia-Min, Wang Yen-Yun, Huang Hurng-Wern, Huang Bin, Lee Ka-Wo, Yuan Shyng-Shiou, Wu Che-Wei, Lin Lee-Shuan, Chan Leong-Per |
Association of the CYP26A1 rs2068888 polymorphism and serum lipid traits in the Chinese Maonan and Han populations. International journal of clinical and experimental pathology 2020 1 10 (12): 11867-11879. Qiu Ling, Yin Rui-Xing, Khounphinith Eksavang, Li Kai-Guang, Wang Duo-Shun, Wu Jin-Zh |
The glucocorticoid receptor represses, whereas C/EBP? can enhance or repress CYP26A1 transcription. iScience 2022 7 25 (7): 104564. Yoo Hong Sik, Rodriguez Adrienne, You Dongjoo, Lee Rebecca A, Cockrum Michael A, Grimes Jack A, Wang Jen-Chywan, Kang Sona, Napoli Joseph |
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- Page last updated:Mar 25, 2024
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