Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 35 Records) |
Query Trace: Peutz-Jeghers Syndrome and STK11[original query] |
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LKB1 gene mutations in Japanese lung cancer patients. Cancer science 2007 Nov 98 (11): 1747-51. Onozato Ryoichi, Kosaka Takayuki, Achiwa Hiroyuki, Kuwano Hiroyuki, Takahashi Takashi, Yatabe Yasushi, Mitsudomi Tetsu |
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 |
Evaluation of the contribution of the three breast cancer susceptibility genes CHEK2, STK11, and PALB2 in non-BRCA1/2 French Canadian families with high risk of breast cancer. Genetic testing and molecular biomarkers 2010 Aug 14 (4): 515-26. Guénard Frédéric, Pedneault Christopher St-Laurent, Ouellette Geneviève, Labrie Yvan, Simard Jacques, , Durocher Franci |
No association between promoter polymorphism of STK11 gene and lung cancer risk in the Korean population. Cancer research and treatment 2009 Dec 41 (4): 4. Sung Jae Sook, Whang Young Mi, Park Kyong Hwa, Ryu Jeong-Seon, Choi Jong Gwon, Seo Jae Hong, Shin Sang Won, Kim Jun Suk, Kim Yeul Ho |
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, |
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 |
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 |
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 |
A single-nucleotide polymorphism in serine-threonine kinase 11, the gene encoding liver kinase B1, is a risk factor for multiple sclerosis. ASN neuro 0 7 (1): . Boullerne Anne I, Skias Demetrios, Hartman Elizabeth M, Testai Fernando D, Kalinin Sergey, Polak Paul E, Feinstein Douglas |
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 |
Characterization of the STK11 splicing variant as a normal splicing isomer in a patient with Peutz-Jeghers syndrome harboring genomic deletion of the STK11 gene. Human genome variation 2016 3 16002. Masuda Kenta, Kobayashi Yusuke, Kimura Tokuhiro, Umene Kiyoko, Misu Kumiko, Nomura Hiroyuki, Hirasawa Akira, Banno Kouji, Kosaki Kenjiro, Aoki Daisuke, Sugano Kokic |
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 manifestations and STK11 germline mutations in Taiwanese patients with Peutz-Jeghers syndrome. Asian journal of surgery 2017 9 41 (5): 480-485. Chiang Jy-Ming, Chen Tse-Chi |
Targeted Genomic Profiling of Female Adnexal Tumors of Probable Wolffian Origin (FATWO). International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists 2018 Aug . Mirkovic Jelena, Dong Fei, Sholl Lynette M, Garcia Elizabeth, Lindeman Neal, MacConaill Laura, Crum Christopher P, Nucci Marisa R, McCluggage W Glenn, Howitt Brooke |
Prenatal diagnosis in a hereditary Peutz-Jeghers syndrome family with high cancer risk. BMC medical genetics 2018 5 19 (1): 66. Wang Zhiqing, Liu Shu, Liu Siping, Wang Yadong, Chen Junsheng, Wu Baopi |
[Identification of a novel STK11 gene mutation in a family affected with hereditary Peutz-Jeghers syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018 2 35 (1): 89-91. Xu Cuiyang, Ma Yue, Cao Fei, Zhao He, Wang Yongjie, Xiao Zewen, Tang Jiebing, Yan Feihu, Sun Peng, Zhang Na, Tao |
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 |
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- |
A novel mutation (c.855delG) in STK11 gene is associated with Peutz-Jeghers syndrome in a Chinese family. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2018 1 50 (3): 312-314. Zhao Zi-Ye, Jiang Yu-Liang, Li Bai-Rong, Yu En-Da, Ning Shou-B |
Clinical and Histologic Overlap and Distinction Among Various Hamartomatous Polyposis Syndromes. Clinical and translational gastroenterology 2019 5 10 (5): 1-9. Gilad Ophir, Rosner Guy, Fliss-Isakov Naomi, Aharon-Kaspi Sivan, Strul Hana, Gluck Nathan, Kariv Revit |
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 p.F354L Germline Mutation in a Case of Multiple Gastrointestinal Tumors. Case reports in gastroenterology 2020 11 14 (3): 547-553. Kojima Yohei, Ohtsuka Kouki, Ishii Shun, Aso Nobuyoshi, Ohki Atsuko, Hashimoto Yoshikazu, Takeuchi Hirohisa, Ohnishi Hiroaki, Abe Nobutsu |
Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants. Hereditary cancer in clinical practice 2021 8 19 (1): 33. Murali Krithika, Dwarte Tanya M, Nikfarjam Mehrdad, Tucker Katherine M, Vaughan Rhys B, Efthymiou Marios, Collins Allison, Spigelman Allan D, Salmon Lucinda, Johns Amber L, Williams David B, Delatycki Martin B, John Thomas, Stoita Ali |
Serine/Threonine Kinase 11 Plays a Canonical Role in Malignant Progression of KRAS -Mutant and GNAS -Wild-Type Intraductal Papillary Mucinous Neoplasms of the Pancreas. Annals of surgery 2021 4 277 (2): e384-e395. Omori Yuko, Ono Yusuke, Morikawa Takanori, Motoi Fuyuhiko, Higuchi Ryota, Yamamoto Masakazu, Hayakawa Yuko, Karasaki Hidenori, Mizukami Yusuke, Unno Michiaki, Furukawa To |
High risk and early onset of cancer in Chinese patients with Peutz-Jeghers syndrome. Frontiers in oncology 2022 8 12 900516. Wang Zhiqing, Wang Zhi, Wang Ying, Wu Jianhua, Yu Zonglin, Chen Chudi, Chen Junsheng, Wu Baoping, Chen |
Is Biannual Surveillance for Pancreatic Cancer Sufficient in Individuals With Genetic Syndromes or Familial Pancreatic Cancer? Journal of the National Comprehensive Cancer Network : JNCCN 2022 6 20 (6): 663-673.e12. Wang Yifan, Cuggia Adeline, Chen Yen-I, Parent Josée, Stanek Agatha, Denroche Robert E, Zhang Amy, Grant Robert C, Domecq Céline, Golesworthy Bryn, Shwaartz Chaya, Borgida Ayelet, Holter Spring, Wilson Julie M, Chong George, O'Kane Grainne M, Knox Jennifer J, Fischer Sandra E, Gallinger Steven, Gao Zu-Hua, Foulkes William D, Waschke Kevin A, Zogopoulos Geor |
Preimplantation genetic testing in two Danish couples affected by Peutz-Jeghers syndrome. Scandinavian journal of gastroenterology 2022 10 58 (3): 314-318. Byrjalsen Anna, Roos Laura, Diemer Tue, Karstensen John Gásdal, Løssl Kristine, Jelsig Anne Mar |
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 |
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- Page last updated:May 06, 2024
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