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Records 1-15

Query Trace: Genetic Diseases, Inborn and STK11[orginal query]

STK11 gene analysis reveals a significant number of splice mutations in Chinese PJS patients. Cancer genetics 2018 Nov . Jiang Yu-Liang, Zhao Zi-Ye, Li Bai-Rong, Wang Hao, Yu En-Da, Ning Shou-B Similar articles in PubMed
Genetic Screening and Analysis of LKB1 Gene in Chinese Patients with Peutz-Jeghers Syndrome. Medical science monitor : international medical journal of experimental and clinical research 2016 Oct 22 3628-3640. Chen Chunyan, Zhang Xiaomei, Wang Deqiang, Wang Fangyu, Pan Jian, Wang Zhenkai, Liu Chang, Wu Lin, Lu Heng, Li Nan, Wei Juan, Shi Hui, Wan Haijun, Zhu Ming, Chen Senqing, Zhou Yun, Zhou Xin, Yang Liu, Liu Jio Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
Polycystic ovary syndrome (PCOS) with melanocytic mucosal macules: the role of STK11 gene polymorphisms in PCOS and Peutz-Jeghers syndrome. International journal of dermatology 2015 Jul . Smith Kathleen J, Germain Margueri Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
Molecular pathogenesis of endometrial cancers in patients with Lynch syndrome. Cancer 2013 Aug 119 (16): 3027-33. Huang Marilyn, Djordjevic Bojana, Yates Melinda S, Urbauer Diana, Sun Charlotte, Burzawa Jennifer, Daniels Molly, Westin Shannon N, Broaddus Russell, Lu Kar Similar articles in PubMed
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2013 Jul 45 (7): 606-11. Resta Nicoletta, Pierannunzio Daniela, Lenato Gennaro Mariano, Stella Alessandro, Capocaccia Riccardo, Bagnulo Rosanna, Lastella Patrizia, Susca Francesco Claudio, Bozzao Cristina, Loconte Daria Carmela, Sabbà Carlo, Urso Emanuele, Sala Paola, Fornasarig Mara, Grammatico Paola, Piepoli Ada, Host Cristina, Turchetti Daniela, Viel Alessandra, Memo Luigi, Giunti Laura, Stigliano Vittoria, Varesco Liliana, Bertario Lucio, Genuardi Maurizio, Lucci Cordisco Emanuela, Tibiletti Maria Grazia, Di Gregorio Carmela, Andriulli Angelo, Ponz de Leon Maurizio, Similar articles in PubMed
Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients. Scandinavian journal of gastroenterology 2013 Jun 48 (6): 672-8. Tanskanen Tomas, Gylfe Alexandra E, Katainen Riku, Taipale Minna, Renkonen-Sinisalo Laura, Mecklin Jukka-Pekka, Järvinen Heikki, Tuupanen Sari, Kilpivaara Outi, Vahteristo Pia, Aaltonen Lauri Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
[Sequence polymorphism of the promoter region of gene STK11 in patients with Peutz-Jeghers syndrome]. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2007 Feb 32 (1): 74-7. Yi Xin, Yao Mao-Jin, Wang Yong-Jun, Tang Jian-Guang, Ning Wen-Feng, Wang Xiang-Ping, Zhou Shi-Quan, Li Chen-Jie, Wang Fei, Xia Kun, Shi Xiao-L Similar articles in PubMed
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 Similar articles in PubMed
Clinical, Pathologic, and Genetic Features of Wilms Tumors With WTX Gene Mutation. Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 0 20 (2): 105-111. Alexandrescu Sanda, Akhavanfard Sara, Harris Marian H, Vargas Sara Similar articles in PubMed

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