Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: TRRAP[original query] |
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RNF43 mutations are recurrent in Chinese patients with mucinous ovarian carcinoma but absent in other subtypes of ovarian cancer. Gene 2013 Nov 531 (1): 112-6. Zou Yang, Wang Feng, Liu Fa-Ying, Huang Mei-Zhen, Li Wei, Yuan Xiao-Qun, Huang Ou-Ping, He Mi |
Mutational analysis of the GNA11, MMP27, FGD1, TRRAP and GRM3 genes in thyroid cancer. Oncology letters 2013 Aug 6 (2): 437-441. Murugan Avaniyapuram Kannan, Yang Chongfei, Xing Mingzh |
Absence of DICER1, CTCF, RPL22, DNMT3A, TRRAP, IDH1 and IDH2 hotspot mutations in patients with various subtypes of ovarian carcinomas. Biomedical reports 2015 Jan 3 (1): 33-37. Zou Yang, Huang Mei-Zhen, Liu Fa-Ying, Yang Bi-Cheng, Wang Li-Qun, Wang Feng, Yu Xiao-Hong, Wan Lei, Wan Xi-DI, Xu Xiao-Yun, Li Wei, Huang Ou-Ping, He Mi |
A novel somatic MAPK1 mutation in primary ovarian mixed germ cell tumors. Oncology reports 2015 Nov . Zou Yang, Deng Wei, Wang Feng, Yu Xiao-Hong, Liu Fa-Ying, Yang Bi-Cheng, Huang Mei-Zhen, Guo Jiu-Bai, Xie Qiu-Hua, He Ming, Huang Ou-Pi |
Germline Variants of Prostate Cancer in Japanese Families. PloS one 2016 11 (10): e0164233. Hayano Takahide, Matsui Hiroshi, Nakaoka Hirofumi, Ohtake Nobuaki, Hosomichi Kazuyoshi, Suzuki Kazuhiro, Inoue Itu |
Appendiceal goblet cell carcinoids and adenocarcinomas ex-goblet cell carcinoid are genetically distinct from primary colorectal-type adenocarcinoma of the appendix. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2018 Jan . Jesinghaus Moritz, Konukiewitz Björn, Foersch Sebastian, Stenzinger Albrecht, Steiger Katja, Muckenhuber Alexander, Groß Claudia, Mollenhauer Martin, Roth Wilfried, Detlefsen Sönke, Weichert Wilko, Klöppel Günter, Pfarr Nicole, Schlitter Anna Melis |
Targeted next-generation sequencing revealed distinct clinicopathologic and molecular features of VCL-ALK RCC: A unique case from an older patient without clinical evidence of sickle cell trait. Pathology, research and practice 2019 9 215 (11): 152651. Wang Xiao-Tong, Fang Ru, Ye Sheng-Bing, Zhang Ru-Song, Li Rui, Wang Xuan, Ji Rong-Hao, Lu Zhen-Feng, Ma Heng-Hui, Zhou Xiao-Jun, Xia Qiu-Yuan, Rao Q |
Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability. American journal of human genetics 2019 3 104 (3): 530-541. Cogné Benjamin, Ehresmann Sophie, Beauregard-Lacroix Eliane, Rousseau Justine, Besnard Thomas, Garcia Thomas, Petrovski Slavé, Avni Shiri, McWalter Kirsty, Blackburn Patrick R, Sanders Stephan J, Uguen Kévin, Harris Jacqueline, Cohen Julie S, Blyth Moira, Lehman Anna, Berg Jonathan, Li Mindy H, Kini Usha, Joss Shelagh, von der Lippe Charlotte, Gordon Christopher T, Humberson Jennifer B, Robak Laurie, Scott Daryl A, Sutton Vernon R, Skraban Cara M, Johnston Jennifer J, Poduri Annapurna, Nordenskjöld Magnus, Shashi Vandana, Gerkes Erica H, Bongers Ernie M H F, Gilissen Christian, Zarate Yuri A, Kvarnung Malin, Lally Kevin P, Kulch Peggy A, Daniels Brina, Hernandez-Garcia Andres, Stong Nicholas, McGaughran Julie, Retterer Kyle, Tveten Kristian, Sullivan Jennifer, Geisheker Madeleine R, Stray-Pedersen Asbjorg, Tarpinian Jennifer M, Klee Eric W, Sapp Julie C, Zyskind Jacob, Holla Øystein L, Bedoukian Emma, Filippini Francesca, Guimier Anne, Picard Arnaud, Busk Øyvind L, Punetha Jaya, Pfundt Rolph, Lindstrand Anna, Nordgren Ann, Kalb Fayth, Desai Megha, Ebanks Ashley Harmon, Jhangiani Shalini N, Dewan Tammie, Coban Akdemir Zeynep H, Telegrafi Aida, Zackai Elaine H, Begtrup Amber, Song Xiaofei, Toutain Annick, Wentzensen Ingrid M, Odent Sylvie, Bonneau Dominique, Latypova Xénia, Deb Wallid, , Redon Sylvia, Bilan Frédéric, Legendre Marine, Troyer Caitlin, Whitlock Kerri, Caluseriu Oana, Murphree Marine I, Pichurin Pavel N, Agre Katherine, Gavrilova Ralitza, Rinne Tuula, Park Meredith, Shain Catherine, Heinzen Erin L, Xiao Rui, Amiel Jeanne, Lyonnet Stanislas, Isidor Bertrand, Biesecker Leslie G, Lowenstein Dan, Posey Jennifer E, Denommé-Pichon Anne-Sophie, , Férec Claude, Yang Xiang-Jiao, Rosenfeld Jill A, Gilbert-Dussardier Brigitte, Audebert-Bellanger Séverine, Redon Richard, Stessman Holly A F, Nellaker Christoffer, Yang Yaping, Lupski James R, Goldstein David B, Eichler Evan E, Bolduc Francois, Bézieau Stéphane, Küry Sébastien, Campeau Philippe |
Multi gene mutation signatures in colorectal cancer patients: predict for the diagnosis, pathological classification, staging and prognosis. BMC cancer 2021 4 21 (1): 380. Zhuang Yan, Wang Hailong, Jiang Da, Li Ying, Feng Lixia, Tian Caijuan, Pu Mingyu, Wang Xiaowei, Zhang Jiangyan, Hu Yuanjing, Liu Pengf |
Integrating SNPs-based genetic risk factor with blood epigenomic response of differentially arsenic-exposed rural subjects reveals disease-associated signaling pathways. Environmental pollution (Barking, Essex : 1987) 2021 10 292 (Pt A): 118279. Rehman Muhammad Yasir Abdur, Briedé Jacco Jan, van Herwijnen Marcel, Krauskopf Julian, Jennen Danyel G J, Malik Riffat Naseem, Kleinjans Jos C |
Two Genetic Mechanisms in Two Siblings with Intellectual Disability, Autism Spectrum Disorder, and Psychosis. Journal of personalized medicine 2022 6 12 (6): . Huang Yu-Shu, Fang Ting-Hsuan, Kung Belle, Chen Chia-Hsia |
Whole-exome sequencing of transforming oral lichen planus reveals mutations in DNA damage repair and apoptosis pathway genes. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology 2022 Feb . Xie Fangyi, Gleue Casey A, Deschaine Maria, Dasari Surendra, Lau Julie S, Sartori-Valinotti Julio C, Meves Alexander, Lehman Julia |
Germline ATM Mutations Detected by Somatic DNA Sequencing in Lethal Prostate Cancer. European urology open science 2023 6 52 72-78. Rafael Grochot, Suzanne Carreira, Susana Miranda, Ines Figueiredo, Claudia Bertan, Jan Rekowski, Wei Yuan, Ana Ferreira, Ruth Riisnaes, Antje Neeb, Bora Gurel, Maria de Los Dolores Fenor de la Maza, Christina Guo, Juliet Carmichael, Daniel Westaby, Joaquin Mateo, Adam Sharp, Terri P McVeigh, Johann De Bo |
Identification of Somatic Mutations in Plasma Cell-Free DNA from Patients with Metastatic Oral Squamous Cell Carcinoma. International journal of molecular sciences 2023 6 24 (12): . Li-Han Lin, Kuo-Wei Chang, Hui-Wen Cheng, Chung-Ji L |
Whole-exome sequencing and bioinformatic analyses revealed differences in gene mutation profiles in papillary thyroid cancer patients with and without benign thyroid goitre background. Frontiers in endocrinology 2023 1 13 1039494. Eng Zing Hong, Abdullah Mardiaty Iryani, Ng Khoon Leong, Abdul Aziz Azlina, Arba'ie Nurul Hannis, Mat Rashid Nurullainy, Mat Junit Sar |
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