HuGE Literature Finder
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| Duplications in 19p13.3 are associated with male infertility. Journal of assisted reproduction and genetics 2019 Aug . Singh Vertika, Bala Renu, Chakraborty Arijit, Rajender Singh, Trivedi Sameer, Singh Kir |
| Contribution of Massive Parallel Sequencing to Diagnosis of Hereditary Ovarian Cancer in the Czech Republic. Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti 2019 32 (Supplementum2): 72-78. Soukupová Jana, Lhotová Klára, Zemánková Petra, Vocka Michal, Janatová Markéta, Stolarová Lenka, Borecká Marianna, Kleiblová Petra, Machácková Eva, Foretová Lenka, Koudová Monika, Lhota Filip, Tavandzis Spiros, Zikán Michal, Stránecký Viktor, Veselá Kamila, Panczak Aleš, Kotlas Jaroslav, Kleibl Zden |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond. JAMA oncology 2015 Apr 1 (1): 23-32. Hansford Samantha, Kaurah Pardeep, Li-Chang Hector, Woo Michelle, Senz Janine, Pinheiro Hugo, Schrader Kasmintan A, Schaeffer David F, Shumansky Karey, Zogopoulos George, Santos Teresa Almeida, Claro Isabel, Carvalho Joana, Nielsen Cydney, Padilla Sarah, Lum Amy, Talhouk Aline, Baker-Lange Katie, Richardson Sue, Lewis Ivy, Lindor Noralane M, Pennell Erin, MacMillan Andree, Fernandez Bridget, Keller Gisella, Lynch Henry, Shah Sohrab P, Guilford Parry, Gallinger Steven, Corso Giovanni, Roviello Franco, Caldas Carlos, Oliveira Carla, Pharoah Paul D P, Huntsman David |
| 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 |
| 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 |
| 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, |
| 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 |
| 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 |
| No association between promoter polymorphism of STK11 gene and lung cancer risk in the Korean population. Cancer research and treatment : official journal of Korean Cancer Association 2009 Dec 41 (4): 4. Sung JS, Whang YM, Park KH, Ryu JS, Choi JG, Seo JH, Shin SW, Kim JS, Kim YH |
| Is pharmacogenomics our future? Metformin, ovulation and polymorphism of the STK11 gene in polycystic ovary syndrome. Pharmacogenomics 2008 Aug 9 (8): 1163-5. Goldenberg Naila, Glueck Charles |
| Ovulatory response to treatment of polycystic ovary syndrome is associated with a polymorphism in the STK11 gene. The Journal of clinical endocrinology and metabolism 2008 Mar 93 (3): 792-800. Legro Richard S, Barnhart Huiman X, Schlaff William D, Carr Bruce R, Diamond Michael P, Carson Sandra A, Steinkampf Michael P, Coutifaris Christos, McGovern Peter G, Cataldo Nicholas A, Gosman Gabriella G, Nestler John E, Giudice Linda C, Ewens Kathryn G, Spielman Richard S, Leppert Phyllis C, Myers Evan R, |
| 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 |
| [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 |
| No evidence for germline mutations of the LKB1/STK11 gene in familial pancreatic carcinoma. Cancer letters 2004 Oct 214 (1): 63-8. Grützmann Robert, McFaul Christopher, Bartsch Detlef K, Sina-Frey Mercedes, Rieder Harald, Koch Rainer, McCarthy Emma, Greenhalf William, Neoptolemos John P, Saeger Hans Detlev, Pilarsky Christi |
| Relative frequency and morphology of cancers in STK11 mutation carriers. Gastroenterology 2004 Jun 126 (7): 1788-94. Lim Wendy, Olschwang Sylviane, Keller Josbert J, Westerman Anne Marie, Menko Fred H, Boardman Lisa A, Scott Rodney J, Trimbath Jill, Giardiello Francis M, Gruber Stephen B, Gille Johan J P, Offerhaus G Johan A, de Rooij Felix W M, Wilson J H Paul, Spigelman Allan D, Phillips Robin K S, Houlston Richard |
| 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 |
| 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 |
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- Page last updated:Jun 22, 2022
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