Human Genome Epidemiology Literature Finder
|
Records 1 - 13 (of 13 Records) |
| Query Trace: Polyps and STK11[original query] |
|---|
| Genotype-phenotype correlations in Peutz-Jeghers syndrome. Journal of medical genetics 2004 May 41 (5): 327-33. Amos C I, Keitheri-Cheteri M B, Sabripour M, Wei C, McGarrity T J, Seldin M F, Nations L, Lynch P M, Fidder H H, Friedman E, Frazier M |
| Truncating mutations in Peutz-Jeghers syndrome are associated with more polyps, surgical interventions and cancers. International journal of colorectal disease 2010 Jan 25 (1): 97-107. Salloch Heidi, Reinacher-Schick Anke, Schulmann Karsten, Pox Christian, Willert Jörg, Tannapfel Andrea, Heringlake Stefan, Goecke Timm O, Aretz Stefan, Stemmler Susanne, Schmiegel Wol |
| Prevalence of germline PTEN, BMPR1A, SMAD4, STK11, and ENG mutations in patients with moderate-load colorectal polyps. Gastroenterology 2013 Jun 144 (7): 1402-9, 1409.e1-5. Ngeow Joanne, Heald Brandie, Rybicki Lisa A, Orloff Mohammed S, Chen Jin Lian, Liu Xiuli, Yerian Lisa, Willis Joseph, Lehtonen Heli J, Lehtonen Rainer, Mester Jessica L, Moline Jessica, Burke Carol A, Church James, Aaltonen Lauri A, Eng Char |
| STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome. Human mutation 2014 Jul 35 (7): 851-8. Wang Zhiqing, Wu Baoping, Mosig Rebecca A, Chen Yulan, Ye Fei, Zhang Yali, Gong Wei, Gong Lanbo, Huang Fei, Wang Xinying, Nie Biao, Zheng Haoxuan, Cui Miao, Wang Yadong, Wang Juan, Chen Chudi, Polydorides Alexandros D, Zhang David Y, Martignetti John A, Jiang |
| Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. Gastroenterology 2015 Sep 149 (3): 604-613.e20. Yurgelun Matthew B, Allen Brian, Kaldate Rajesh R, Bowles Karla R, Judkins Thaddeus, Kaushik Praveen, Roa Benjamin B, Wenstrup Richard J, Hartman Anne-Renee, Syngal Sap |
| Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndrome. Familial cancer 2015 Sep 14 (3): 455-61. Borun Pawel, De Rosa Marina, Nedoszytko Boguslaw, Walkowiak Jaroslaw, Plawski Andrz |
| Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome. BMC gastroenterology 2015 15 (1): 166. Huang Zhiheng, Miao Shijian, Wang Lin, Zhang Ping, Wu Bingbing, Wu Jie, Huang Yi |
| Disease pattern in Danish patients with Peutz-Jeghers syndrome. International journal of colorectal disease 2016 Mar . Jelsig A M, Qvist N, Sunde L, Brusgaard K, Hansen Tvo, Wikman F P, Nielsen C B, Nielsen I K, Gerdes A M, Bojesen A, Ousager L |
| Clinical and Genetic Study of Children With Peutz-Jeghers Syndrome Identifies a High Frequency of STK11 De Novo Mutation. Journal of pediatric gastroenterology and nutrition 2018 10 68 (2): 199-206. Zhao Hong-Mei, Yang Yong-Jia, Duan Jia-Qi, Ouyang Hong-Juan, Liu Li, Yi Li-Chun, Xiao Zheng-Hui, Zheng Yu, Peng Lv, Attard Thomas M, Li Ding-You, You Jie- |
| Novel germline STK11 variants and breast cancer phenotype identified in an Indian cohort of Peutz-Jeghers syndrome. Human molecular genetics 2019 1 28 (11): 1885-1893. Lipsa Anuja, Kowtal Pradnya, Sarin Raj |
| [Diagnosis and treatment for 46 cases of Peutz-Jeghers syndrome]. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2019 1 43 (12): 1323-1327. Jia Yan, Fu Hao, Li Na, Kang Qian, Sheng Jianq |
| Clinical and Genetic Analyses of 38 Chinese Patients with Peutz-Jeghers Syndrome. BioMed research international 2020 5 2020 9159315. Wu Bo-Da, Wang Yong-Jun, Fan Liang-Liang, Huang Hui, Zhou Peng, Yang Mei, Shi Xiao-L |
| STK11 Causative Variants and Copy Number Variations Identified in Thai Patients With Peutz-Jeghers Syndrome. Cureus 2023 3 15 (2): e34495. Chiraphapphaiboon Wannasiri, Thongnoppakhun Wanna, Limjindaporn Thawornchai, Sawasdichai Sunisa, Roothumnong Ekkapong, Prangphan Kanjana, Pamornpol Benjaporn, Limwongse Chanin, Pithukpakorn Man |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 01, 2023
- Content source: