Human Genome Epidemiology Literature Finder
|
Records 1 - 8 (of 8 Records) |
| Query Trace: KRT5[original query] |
|---|
| New common variants affecting susceptibility to basal cell carcinoma. Nature genetics 2009 Aug 41 (8): 909-14. Stacey Simon N, Sulem Patrick, Masson Gisli, Gudjonsson Sigurjon A, Thorleifsson Gudmar, Jakobsdottir Margret, Sigurdsson Asgeir, Gudbjartsson Daniel F, Sigurgeirsson Bardur, Benediktsdottir Kristrun R, Thorisdottir Kristin, Ragnarsson Rafn, Scherer Dominique, Hemminki Kari, Rudnai Peter, Gurzau Eugene, Koppova Kvetoslava, Botella-Estrada Rafael, Soriano Virtudes, Juberias Pablo, Saez Berta, Gilaberte Yolanda, Fuentelsaz Victoria, Corredera Cristina, Grasa Matilde, Höiom Veronica, Lindblom Annika, Bonenkamp Johannes J, van Rossum Michelle M, Aben Katja K H, de Vries Esther, Santinami Mario, Di Mauro Maria G, Maurichi Andrea, Wendt Judith, Hochleitner Pia, Pehamberger Hubert, Gudmundsson Julius, Magnusdottir Droplaug N, Gretarsdottir Solveig, Holm Hilma, Steinthorsdottir Valgerdur, Frigge Michael L, Blondal Thorarinn, Saemundsdottir Jona, Bjarnason Hjördis, Kristjansson Kristleifur, Bjornsdottir Gyda, Okamoto Ichiro, Rivoltini Licia, Rodolfo Monica, Kiemeney Lambertus A, Hansson Johan, Nagore Eduardo, Mayordomo José I, Kumar Rajiv, Karagas Margaret R, Nelson Heather H, Gulcher Jeffrey R, Rafnar Thorunn, Thorsteinsdottir Unnur, Olafsson Jon H, Kong Augustine, Stefansson Ka |
| Novel and recurrent mutations in Keratin 5 and 14 in Korean patients with Epidermolysis bullosa simplex. Journal of dermatological science 2010 1 57 (2): 90-4. Kang Tae-Won, Lee Jeong Seon, Kim Song-Ee, Oh Se-Woong, Kim Soo-Ch |
| Mutations in KRT5 and KRT14 cause epidermolysis bullosa simplex in 75% of the patients. The British journal of dermatology 2011 Mar 164 (3): 637-44. Bolling M C, Lemmink H H, Jansen G H L, Jonkman M |
| Novel sporadic and recurrent mutations in KRT5 and KRT14 genes in Polish epidermolysis bullosa simplex patients: further insights into epidemiology and genotype-phenotype correlation. Journal of applied genetics 2015 Oct . Wertheim-Tysarowska K, O?dak M, Giza A, Kutkowska-Ka?mierczak A, Sota J, Przybylska D, Wo?niak K, ?niegórska D, Niepokój K, Sobczy?ska-Tomaszewska A, Rygiel A M, P?oski R, Bal J, Kowalewski |
| Known and novel mutations responsible for epidermolysis bullosa simplex cases in a Chinese population. Experimental and therapeutic medicine 2019 11 18 (6): 4661-4664. Zhang Jia, Ding Yu, Li Ming, Yao Zhirong, Zhuang Y |
| Next-generation sequencing through multigene panel testing for the diagnosis of hereditary epidermolysis bullosa in Chinese population. Clinical genetics 2020 6 98 (2): 179-184. Chen Fuying, Huang Linting, Li Changcan, Zhang Jia, Yang Weiqin, Zhang Beibei, Li Huaguo, Deng Dan, Liang Jianying, Shen Jinwen, Yao Zhirong, Li Mi |
| Epidermolysis Bullosa in Chinese Patients: Genetic Analysis and Mutation Landscape in 57 Pedigrees and Sporadic Cases. Acta dermato-venereologica 2021 5 101 (7): adv00503. Yu Yueqian, Wang Zhenzhen, Mi Zihao, Sun Lele, Fu Xi'an, Yu Gongqi, Pang Zheng, Liu Hong, Zhang Fur |
| Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa. Pediatric dermatology 2023 10 . Shir Bergson, Daniel Daniely, David Bomze, Janan Mohamad, Kiril Malovitski, Odile Meijers, Valeria Briskin, Ofer Bihari, Natalia Malchin, Shirli Israeli, Jacob Mashiah, Tzipora Falik-Zaccai, Emily Avitan-Hersh, Marina Eskin-Schwartz, Stavit Allon-Shalev, Ofer Sarig, Eli Sprecher, Liat Samuel |
- Page last reviewed:Feb 1, 2024
- Content source: