Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: ALOX12B[original query] |
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Candidate gene approach evaluates association between innate immunity genes and breast cancer risk in Korean women. Carcinogenesis 2009 Sep 30 (9): 1528-31. Lee Ji-Young, Park Ae Kyung, Lee Kyoung-Mu, Park Sue K, Han Sohee, Han Wonshik, Noh Dong-Young, Yoo Keun-Young, Kim Ho, Chanock Stephen J, Rothman Nathaniel, Kang Daeh |
Polymorphisms in innate immunity genes and lung cancer risk in Xuanwei, China. Environmental and molecular mutagenesis 2009 May 50 (4): 285-90. Shen Min, Vermeulen Roel, Rajaraman Preetha, Menashe Idan, He Xingzhou, Chapman Robert S, Yeager Meredith, Thomas Gilles, Burdett Laurie, Hutchinson Amy, Yuenger Jeff, Chanock Stephen, Lan Qi |
Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B. The Journal of investigative dermatology 2009 Jun 129 (6): 1421-8. Eckl Katja-Martina, de Juanes Silvia, Kurtenbach Janine, Nätebus Marc, Lugassy Jenny, Oji Vinzenz, Traupe Heiko, Preil Marie-Luise, Martínez Francisco, Smolle Josef, Harel Avikam, Krieg Peter, Sprecher Eli, Hennies Hans |
Mutation update for CYP4F22 variants associated with autosomal recessive congenital ichthyosis. Human mutation 2018 7 39 (10): 1305-1313. Hotz Alrun, Bourrat Emmanuelle, Küsel Julia, Oji Vinzenz, Alter Svenja, Hake Lisanne, Korbi Mouna, Ott Hagen, Hausser Ingrid, Zimmer Andreas D, Fischer Judi |
Congenital ichthyosiform erythroderma with a novel variant in ABCA12 in a Chinese patient. Pediatric investigation 2020 8 4 (1): 51-54. Yang Zhou, Qi Zhan, Xu Zhe, Li Wei, Ma L |
High rate of self-improving phenotypes in children with non-syndromic congenital ichthyosis: case series from south-western Germany. Journal of the European Academy of Dermatology and Venereology : JEADV 2021 7 35 (11): 2293-2299. Frommherz L, Krause A, Kopp J, Hotz A, Hübner S, Reimer-Taschenbrecker A, Casetti F, Zirn B, Fischer J, Has |
The impact of CPT1B rs470117, LEPR rs1137101 and BDNF rs6265 polymorphisms on the risk of developing obesity in an Italian population. Obesity research & clinical practice 2021 Jun . Ricci Claudia, Marzocchi Carlotta, Riolo Giulia, Ciuoli Cristina, Benenati Nicoletta, Bufano Annalisa, Tirone Andrea, Voglino Costantino, Vuolo Giuseppe, Castagna Maria Grazia, Cantara Silv |
Genetic Etiology of Ichthyosis in Turkish Patients: Next-generation Sequencing Identified Seven Novel Mutations. Medeniyet medical journal 2022 6 37 (2): 126-130. Saat Hanife, Sahin Ibrahim, Duzkale Neslihan, Gonul Muzeyyen, Bahsi Ta |
Genotype of autosomal recessive congenital ichthyosis from a tertiary care center in India. Pediatric dermatology 2022 4 39 (3): 420-424. Chiramel Minu Jose, Mathew Lydia, Athirayath Rekha, Chapla Aaron, Sathishkumar Dharshini, Mani Thenmozhi, Danda Sumita, George Re |
Oncogenic alterations reveal key strategies for precision oncology in melanoma treatment. Annals of translational medicine 2022 12 10 (22): 1246. Sun Wei, Zhao Fang, Hu Tu, Wu Zhiqiang, Xu Yu, Dong Yan, Zheng Biqiang, Wang Chunmeng, Yan Wangjun, Zhu Xiaoli, Wu Jian, McKay Michael J, Arozarena Imanol, Alos Llucia, Teixido Cristina, Chen Yo |
A case of self-improving collodion ichthyosis associated with a rare variant of the ALOX12B gene. Dermatology online journal 2023 4 29 (1): . Amoedo P, Cerejeira A, Pacheco J, Cruz M J, Mota |
Cross-sectional study on autosomal recessive congenital ichthyoses: association of genotype with disease severity, phenotypic and ultrastructural features in 74 Italian patients. Dermatology (Basel, Switzerland) 2024 4 . Andrea Diociaiuti, Marialuisa Corbeddu, Sabrina Rossi, Elisa Pisaneschi, Claudia Cesario, Angelo Giuseppe Condorelli, Tonia Samela, Simona Giancristoforo, Adriano Angioni, Giovanna Zambruno, Antonio Novelli, Rita Alaggio, Damiano Abeni, May El Hach |
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- Page last updated:Apr 22, 2024
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