Human Genome Epidemiology Literature Finder
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Records 1 - 26 (of 26 Records) |
| Query Trace: Disease and GNA11[original query] |
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| Mutations in GNA11 in uveal melanoma. The New England journal of medicine 2010 Dec 363 (23): 2191-9. Van Raamsdonk Catherine D, Griewank Klaus G, Crosby Michelle B, Garrido Maria C, Vemula Swapna, Wiesner Thomas, Obenauf Anna C, Wackernagel Werner, Green Gary, Bouvier Nancy, Sozen M Mert, Baimukanova Gail, Roy Ritu, Heguy Adriana, Dolgalev Igor, Khanin Raya, Busam Klaus, Speicher Michael R, O'Brien Joan, Bastian Boris |
| Routine multiplex mutational profiling of melanomas enables enrollment in genotype-driven therapeutic trials. PloS one 2012 7 (4): e35309. Lovly Christine M, Dahlman Kimberly Brown, Fohn Laurel E, Su Zengliu, Dias-Santagata Dora, Hicks Donna J, Hucks Donald, Berry Elizabeth, Terry Charles, Duke MarKeesa, Su Yingjun, Sobolik-Delmaire Tammy, Richmond Ann, Kelley Mark C, Vnencak-Jones Cindy L, Iafrate A John, Sosman Jeffrey, Pao Willi |
| Patient survival in uveal melanoma is not affected by oncogenic mutations in GNAQ and GNA11. British journal of cancer 2013 Jul 109 (2): 493-6. Koopmans A E, Vaarwater J, Paridaens D, Naus N C, Kilic E, de Klein A, |
| Analysis of AP2S1, a calcium-sensing receptor regulator, in familial and sporadic isolated hypoparathyroidism. The Journal of clinical endocrinology and metabolism 2014 Mar 99 (3): E469-73. Lambert Anne-Sophie, Grybek Virginie, Francou Bruno, Esterle Laure, Bertrand Guylène, Bouligand Jérôme, Guiochon-Mantel Anne, Hieronimus Sylvie, Voitel Dorit, Soskin Sylvie, Magdelaine Corinne, Lienhardt Anne, Silve Caroline, Linglart Agn |
| Metastatic disease in uveal melanoma: importance of a genetic profile? Melanoma research 2015 Oct 25 (5): 447-9. Van Beek Jackelien G M, Koopmans Anna E, Vaarwater Jolanda, Verdijk Rob M, de Klein Annelies, Naus Nicole C, Kiliç Emi |
| Whole-genome copy-number analysis identifies new leads for chromosomal aberrations involved in the oncogenesis and metastastic behavior of uveal melanomas. Melanoma research 2015 Mar . van Engen-van Grunsven Adriana C H, Baar Marjolein P, Pfundt Rolph, Rijntjes Jos, Küsters-Vandevelde Heidi V N, Delbecq Ann-Laure, Keunen Jan E, Klevering Jeroen B, Wesseling Pieter, Blokx Willeke A M, Groenen Patricia J T |
| Genetic Background of Iris Melanomas and Iris Melanocytic Tumors of Uncertain Malignant Potential. Ophthalmology 2018 Jan . van Poppelen Natasha M, Vaarwater Jolanda, Mudhar Hardeep S, Sisley Karen, Rennie Ian G, Rundle Paul, Brands Tom, van den Bosch Quincy C C, Mensink Hanneke W, de Klein Annelies, Kiliç Emine, Verdijk Robert |
| Heterogeneity of GNAQ/11 mutation inversely correlates with the metastatic rate in uveal melanoma. The British journal of ophthalmology 2019 Sep . Liang Chen, Peng Lan Ya, Zou Ming, Chen Xuemei, Chen Yingying, Chen Hou, Xiao Lirong, Yan Naihong, Zhang Junjun, Zhao Qing, Huang |
| Do GNAQ and GNA11 Differentially Affect Inflammation and HLA Expression in Uveal Melanoma? Cancers 2019 8 11 (8): . van Weeghel Christiaan, Wierenga Annemijn P A, Versluis Mieke, van Hall Thorbald, van der Velden Pieter A, Kroes Wilma G M, Pfeffer Ulrich, Luyten Gregorius P M, Jager Martine |
| Characterization of the Pathophysiological Role of CD47 in Uveal Melanoma. Molecules (Basel, Switzerland) 2019 7 24 (13): . Petralia Maria Cristina, Mazzon Emanuela, Fagone Paolo, Russo Andrea, Longo Antonio, Avitabile Teresio, Nicoletti Ferdinando, Reibaldi Michele, Basile Maria Sof |
| Heterogeneity in Mitogen-Activated Protein Kinase (MAPK) Pathway Activation in Uveal Melanoma With Somatic GNAQ and GNA11 Mutations. Investigative ophthalmology & visual science 2019 Jun 60 (7): 2474-2480. Boru Getachew, Cebulla Colleen M, Sample Klarke M, Massengill James B, Davidorf Frederick H, Abdel-Rahman Mohamed |
| Distinct co-acquired alterations and genomic evolution during TKI treatment in non-small-cell lung cancer patients with or without acquired T790M mutation. Oncogene 2019 Nov . Jin Ying, Bao Hua, Le Xiuning, Fan Xiaojun, Tang Ming, Shi Xun, Zhao Jun, Yan Junrong, Xu Yang, Quek Kelly, Elamin Yasir Y, Zhang Jianhua, Futreal P Andrew, Wistuba Ignacio I, Heymach John V, Lou Guangyuan, Shao Lan, He Qiong, Lin Chen, Wu Xue, Shao Yang W, Wang Xiaonan, He Jiachen, Chen Yamei, Stebbing Justin, Chen Ming, Zhang Jianjun, Yu Xinm |
| Distinct Mutation Patterns Reveal Melanoma Subtypes and Influence Immunotherapy Response in Advanced Melanoma Patients. Cancers 2020 8 12 (9): . Hilke Franz J, Sinnberg Tobias, Gschwind Axel, Niessner Heike, Demidov German, Amaral Teresa, Ossowski Stephan, Bonzheim Irina, Röcken Martin, Riess Olaf, Garbe Claus, Schroeder Christopher, Forschner Andr |
| Dynamic analysis of circulating tumor DNA to predict prognosis and monitor therapeutic response in metastatic relapsed cervical cancer. International journal of cancer 2020 Oct . Tian Xiaoyuan, Ge Dongcen, Zhang Feng, Zhang Bocheng, Bai Wanting, Xu Xiaoying, Li Zongjuan, Cao Ying, Li Peiying, Zou Kun, Zou Liju |
| Molecular Genetics of Conjunctival Melanoma and Prognostic Value of TERT Promoter Mutation Analysis. International journal of molecular sciences 2021 6 22 (11): . van Poppelen Natasha M, van Ipenburg Jolique A, van den Bosch Quincy, Vaarwater Jolanda, Brands Tom, Eussen Bert, Magielsen Frank, Dubbink Hendrikus J, Paridaens Dion, Brosens Erwin, Naus Nicole, de Klein Annelies, Kiliç Emine, Verdijk Robert |
| Uveal melanoma: laboratory advances and new frontiers in patient care. Current opinion in ophthalmology 2021 (3): 301-308. Xu Timothy T, Moser Justin C, Dalvin Lauren |
| Uveal melanoma diagnosis and current treatment options (Review). Experimental and therapeutic medicine 2021 10 22 (6): 1428. Branisteanu Daniel Constantin, Bogdanici Camelia Margareta, Branisteanu Daciana Elena, Maranduca Minela Aida, Zemba Mihail, Balta Florian, Branisteanu Catalina Ioana, Moraru Andreea Da |
| BRAF, NRAS, KIT, TERT, GNAQ/GNA11 Mutation Profile and Histomorphological Analysis of Anorectal Melanomas: A Clinicopathologic Study. Turk patoloji dergisi 2022 6 39 (1): 23-30. Taskin Orhun Cig, Sari Sule Ozturk, Yilmaz Ismail, Hurdogan Ozge, Keskin Metin, Buyukbabani Nesimi, Gulluoglu Mi |
| Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants. Journal of medical genetics 2022 3 60 (2): 163-173. Mussa Alessandro, Leoni Chiara, Iacoviello Matteo, Carli Diana, Ranieri Carlotta, Pantaleo Antonino, Buonuomo Paola Sabrina, Bagnulo Rosanna, Ferrero Giovanni Battista, Bartuli Andrea, Melis Daniela, Maitz Silvia, Loconte Daria Carmela, Turchiano Antonella, Piglionica Marilidia, De Luisi Annunziata, Susca Francesco Claudio, Bukvic Nenad, Forleo Cinzia, Selicorni Angelo, Zampino Giuseppe, Onesimo Roberta, Cappuccio Gerarda, Garavelli Livia, Novelli Chiara, Memo Luigi, Morando Carla, Della Monica Matteo, Accadia Maria, Capurso Martina, Piscopo Carmelo, Cereda Anna, Di Giacomo Marilena Carmela, Saletti Veronica, Spinelli Alessandro Mauro, Lastella Patrizia, Tenconi Romano, Dvorakova Veronika, Irvine Alan D, Resta Nicolet |
| Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders. European journal of endocrinology 2022 1 186 (3): 351-366. Canaff Lucie, Guarnieri Vito, Kim Yoojung, Wong Betty Y L, Nolin-Lapalme Alexis, Cole David E C, Minisola Salvatore, Eller-Vainicher Cristina, Cetani Filomena, Repaci Andrea, Turchetti Daniela, Corbetta Sabrina, Scillitani Alfredo, Goltzman Dav |
| Genetic and clinical screening for hereditary primary hyperparathyroidism in a large Chinese cohort: a single-center study. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2023 7 . An Song, Yi Yang, Yue Jiang, Min Nie, Yan Jiang, Mei Li, Weibo Xia, Xiaoping Xing, Ou Wa |
| Trametinib in Patients With NF1-, GNAQ-, or GNA11-Mutant Tumors: Results From the NCI-MATCH ECOG-ACRIN Trial (EAY131) Subprotocols S1 and S2. JCO precision oncology 2023 4 7 e2200421. Wisinski Kari B, Flamand Yael, Wilson Melissa A, Luke Jason J, Tawbi Hussein A, Hong Fangxin, Mitchell Edith P, Zwiebel James A, Chen Helen, Gray Robert J, Li Shuli, McShane Lisa M, Rubinstein Lawrence V, Patton David, Williams P Mickey, Hamilton Stanley R, Behrens Robert J, Pennington Kathryn P, Conley Barbara A, Arteaga Carlos L, Harris Lyndsay N, O'Dwyer Peter J, Chen Alice P, Flaherty Keith |
| GNA11 variants identified in patients with hypercalcemia or hypocalcemia. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2023 3 . Howles Sarah A, Gorvin Caroline M, Cranston Treena, Rogers Angela, Gluck Anna K, Boon Hannah, Gibson Kate, Rahman Mushtaqur, Root Allen, Nesbit M Andrew, Hannan Fadil M, Thakker Rajesh |
| Genetic testing for familial hyperparathyroidism: clinical-genetic profile in a Mediterranean cohort. Frontiers in endocrinology 2023 10 14 1244361. Isabel Mazarico-Altisent, Ismael Capel, Neus Baena, Maria Rosa Bella-Cueto, Santi Barcons, Xavier Guirao, Rocío Pareja, Andreea Muntean, Valeria Arsentales, Assumpta Caixàs, Mercedes Rig |
| Impact of Driver Mutations on Metastasis-Free Survival in Uveal Melanoma: A Meta-Analysis. Cancers 2024 7 16 (14): . David Lamas-Francis, Carmen Antía Rodríguez-Fernández, Elia de Esteban-Maciñeira, Paula Silva-Rodríguez, María Pardo, Manuel Bande-Rodríguez, María José Blanco-Teijei |
| Identification and validation of a costimulatory molecule-related signature to predict the prognosis for uveal melanoma patients. Scientific reports 2024 4 14 (1): 9146. Minyao Zhao, Yue Yu, Zhengyu So |
- Page last reviewed:Feb 1, 2024
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