Human Genome Epidemiology Literature Finder
|
Records 1 - 13 (of 13 Records) |
| Query Trace: Disease and FOXL2[original query] |
|---|
| Prognostic significance of FOXL2 mutation and mRNA expression in adult and juvenile granulosa cell tumors of the ovary. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2011 Oct 24 (10): 1360-7. D'Angelo Emanuela, Mozos Ana, Nakayama Daiei, Espinosa Iñigo, Catasus Lluis, Muñoz Josefina, Prat Jai |
| SNP rs1511412 in FOXL2 gene as a risk factor for keloid by meta analysis. International journal of clinical and experimental medicine 2015 8 (2): 2766-71. Lu Wensheng, Zheng Xiaodong, Liu Shengli, Ding Maoqian, Xie Jian, Yao Xiuhua, Zhang Lanfang, Hu B |
| Prognostic factors in the myoepithelial-like spindle cell type of metaplastic breast cancer. Virchows Archiv : an international journal of pathology 2016 May . Leo Fabian, Bartels Stephan, Mägel Lavinia, Framke Theodor, Büsche Guntram, Jonigk Danny, Christgen Matthias, Lehmann Ulrich, Kreipe Ha |
| Mutational heterogeneity in non-serous ovarian cancers. Scientific reports 2017 Aug 7 (1): 9728. Teer Jamie K, Yoder Sean, Gjyshi Anxhela, Nicosia Santo V, Zhang Chaomei, Monteiro Alvaro N |
| Mutational Landscape of Ovarian Adult Granulosa Cell Tumors from Whole Exome and Targeted TERT Promoter Sequencing. Molecular cancer research : MCR 2018 9 17 (1): 177-185. Alexiadis Maria, Rowley Simone M, Chu Simon, Leung Dilys T H, Stewart Colin J R, Amarasinghe Kaushalya C, Campbell Ian G, Fuller Peter |
| KMT2D/MLL2 inactivation is associated with recurrence in adult-type granulosa cell tumors of the ovary. Nature communications 2018 Jun 9 (1): 2496. Hillman R Tyler, Celestino Joseph, Terranova Christopher, Beird Hannah C, Gumbs Curtis, Little Latasha, Nguyen Tri, Thornton Rebecca, Tippen Samantha, Zhang Jianhua, Lu Karen H, Gershenson David M, Rai Kunal, Broaddus Russell R, Futreal P Andr |
| Novel Genetic Variants of Sporadic Atrial Septal Defect (ASD) in a Chinese Population Identified by Whole-Exome Sequencing (WES). Medical science monitor : international medical journal of experimental and clinical research 2018 Mar 24 1340-1358. Liu Yong, Cao Yu, Li Yaxiong, Lei Dongyun, Li Lin, Hou Zong Liu, Han Shen, Meng Mingyao, Shi Jianlin, Zhang Yayong, Wang Yi, Niu Zhaoyi, Xie Yanhua, Xiao Benshan, Wang Yuanfei, Li Xiao, Yang Lirong, Wang Wenju, Jiang Liho |
| Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children. American journal of human genetics 2018 2 102 (3): 487-493. Bashamboo Anu, Eozenou Caroline, Jorgensen Anne, Bignon-Topalovic Joelle, Siffroi Jean-Pierre, Hyon Capucine, Tar Attila, Nagy Péter, Sólyom Janos, Halász Zita, Paye-Jaouen Annnabel, Lambert Sophie, Rodriguez-Buritica David, Bertalan Rita, Martinerie Laetitia, Rajpert-De Meyts Ewa, Achermann John C, McElreavey K |
| A Novel FOXL2 Mutation Implying Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Type I. Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2018 1 45 (1): 203-211. Li Fang, Chai Peiwei, Fan Jiayan, Wang Xi, Lu Wenjuan, Li Jin, Ge Shengfang, Jia Renbing, Zhang He, Fan Xianq |
| Genomic profiling of primary and recurrent adult granulosa cell tumors of the ovary. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2020 Mar . Da Cruz Paula Arnaud, da Silva Edaise M, Segura Sheila E, Pareja Fresia, Bi Rui, Selenica Pier, Kim Sarah H, Ferrando Lorenzo, Vahdatinia Mahsa, Soslow Robert A, Vidal August, Gatius Sonia, Przybycin Christopher G, Abu-Rustum Nadeem R, Matias-Guiu Xavier, Rubin Brian P, Reis-Filho Jorge S, DeLair Deborah F, Weigelt Brit |
| FOXL2 homozygous genotype and chromosome instability are associated with recurrence in adult granulosa cell tumors of the ovary. Oncotarget 2020 2 11 (4): 419-428. Kraus Francois, Dremaux Julie, Altakfi Wajd, Goux Magalie, Pontois Léa, Sevestre Henri, Trudel Stéphan |
| Genetic etiologic analysis in 74 Chinese Han women with idiopathic premature ovarian insufficiency by combined molecular genetic testing. Journal of assisted reproduction and genetics 2021 Feb . Shen Jiandong, Qu Dianyun, Gao Yan, Sun Fangxi, Xie Jiazi, Sun Xueping, Wang Daowu, Ma Xiang, Cui Yugui, Liu Jiayin, Diao Feiya |
| Genetic variations in triple-negative breast cancers undergoing neo-adjuvant chemotherapy. Cancer drug resistance (Alhambra, Calif.) 2022 5 2 (3): 877-884. Mori Miki, Watanabe Tomoko, Akashi-Tanaka Sadako, Ueda Kumiko, Makino Reiko, Hirota Yuko, Nakamura Sei |
- Page last reviewed:Feb 1, 2024
- Content source: