Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: USP8[original query] |
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Genome-wide association study identifies candidate genes for male fertility traits in humans.
American journal of human genetics 2012 Jun 90 (6): 950-61. Kosova Gülüm, Scott Nicole M, Niederberger Craig, Prins Gail S, Ober Caro |
[Study on the association of USP8 gene polymorphisms with male infertility in ethnic Han Chinese from Sichuan]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2015 Apr 32 (2): 269-73. Ding Min, Li Lingxiao, Ding Xianping, Ren Huaying, Zhong Ro |
The USP8 mutational status may predict drug susceptibility in corticotroph adenomas of Cushing's disease. European journal of endocrinology / European Federation of Endocrine Societies 2015 Nov . Hayashi Kyohei, Inoshita Naoko, Kawaguchi Kohei, Ardisasmita Arif Ibrahim, Suzuki Hisanori, Fukuhara Noriaki, Okada Mitsuo, Nishioka Hiroshi, Takeuchi Yasuhiro, Komada Masayuki, Takeshita Akira, Yamada Sho |
Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease. The Journal of clinical endocrinology and metabolism 2017 May . Faucz Fabio R, Tirosh Amit, Tatsi Christina, Berthon Annabel, Hernández-Ramírez Laura C, Settas Nikolaos, Angelousi Anna, Correa Ricardo, Papadakis Georgios Z, Chittiboina Prashant, Quezado Martha, Pankratz Nathan, Lane John, Dimopoulos Aggeliki, Mills James L, Lodish Maya, Stratakis Constantine |
Genetic landscape of sporadic vestibular schwannoma. Journal of neurosurgery 2017 Apr 1-12. Håvik Aril Løge, Bruland Ove, Myrseth Erling, Miletic Hrvoje, Aarhus Mads, Knappskog Per-Morten, Lund-Johansen Mort |
Somatic USP8 mutations are frequent events in corticotroph tumor progression causing Nelson's tumor. European journal of endocrinology 2017 10 178 (1): 57-63. Pérez-Rivas Luis G, Theodoropoulou Marily, Puar Troy H, Fazel Julia, Stieg Mareike R, Ferraù Francesco, Assié Guillaume, Gadelha Monica R, Deutschbein Timo, Fragoso Maria C, Kusters Benno, Saeger Wolfgang, Honegger Jürgen, Buchfelder Michael, Korbonits Márta, Bertherat Jérôme, Stalla Günter K, Hermus Ad R, Beuschlein Felix, Reincke Mart |
The USP8 mutational status may predict long-term remission in patients with Cushing's disease. Clinical endocrinology 2018 Jun . Albani Adriana, Pérez-Rivas Luis G, Dimopoulou Christina, Zopp Stephanie, Colón-Bolea Paula, Roeber Sigrun, Honegger Jürgen, Flitsch Jörg, Rachinger Walter, Buchfelder Michael, Stalla Günter K, Herms Jochen, Reincke Martin, Theodoropoulou Mari |
Clinical characteristics and surgical outcome in USP8-mutated human adrenocorticotropic hormone-secreting pituitary adenomas. Endocrine 2019 Feb 63 (2): 240-246. Losa Marco, Mortini Pietro, Pagnano Angela, Detomas Mario, Cassarino Maria Francesca, Pecori Giraldi Frances |
A mutational signature associated with alcohol consumption and prognostically significantly mutated driver genes in esophageal squamous cell carcinoma. Annals of oncology : official journal of the European Society for Medical Oncology 2018 Jan . Li X C, Wang M Y, Yang M, Dai H J, Zhang B F, Wang W, Chu X L, Wang X, Zheng H, Niu R F, Zhang W, Chen K |
Cushing's disease due to somatic USP8 mutations: a systematic review and meta-analysis. Pituitary 2019 Jul . Wanichi Ingrid Quevedo, de Paula Mariani Beatriz Marinho, Frassetto Fernando Pereira, Siqueira Sheila Aparecida Coelho, de Castro Musolino Nina Rosa, Cunha-Neto Malebranche Berardo Carneiro, Ochman Gilberto, Cescato Valter Angelo Sperling, Machado Marcio Carlos, Trarbach Ericka Barbosa, Bronstein Marcello Delano, Fragoso Maria Candida Barisson Villar |
Driver mutations in USP8 wild-type Cushing's disease. Neuro-oncology 2019 6 21 (10): 1273-1283. Sbiera Silviu, Perez-Rivas Luis Gustavo, Taranets Lyudmyla, Weigand Isabel, Flitsch Jörg, Graf Elisabeth, Monoranu Camelia-Maria, Saeger Wolfgang, Hagel Christian, Honegger Jürgen, Assie Guillaume, Hermus Ad R, Stalla Günter K, Herterich Sabine, Ronchi Cristina L, Deutschbein Timo, Reincke Martin, Strom Tim M, Popov Nikita, Theodoropoulou Marily, Fassnacht Mart |
Impact of USP8 Gene Mutations on Protein Deregulation in Cushing Disease. The Journal of clinical endocrinology and metabolism 2019 Mar . Weigand Isabel, Knobloch Lisanne, Flitsch Jörg, Saeger Wolfgang, Monoranu Camelia M, Höfner Kerstin, Herterich Sabine, Rotermund Roman, Ronchi Cristina L, Buchfelder Michael, Glatzel Markus, Hagel Christian, Fassnacht Martin, Deutschbein Timo, Sbiera Silv |
SST5 expression and USP8 mutation in functioning and silent corticotroph pituitary tumors. Endocrine connections 2020 2 9 (3): 243-53. Castellnou Solène, Vasiljevic Alexandre, Lapras Veronique, Raverot Véronique, Alix Eudeline, Borson-Chazot Françoise, Jouanneau Emmanuel, Raverot Gerald, Lasolle Hélè |
USP8 Mutations and Cell Cycle Regulation in Corticotroph Adenomas. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2020 2 52 (2): 117-123. Martins Clarissa Silva, Camargo Renata Costa, Coeli-Lacchini Fernanda Borchers, Saggioro Fabiano Pinto, Moreira Ayrton Custodio, de Castro Margar |
USP8, USP48, and BRAF mutations differ in their genotype-phenotype correlation in Asian Indian patients with Cushing's disease. Endocrine 2021 10 75 (2): 549-559. Abraham Ananth P, Pai Rekha, Beno Daniel L, Chacko Geeta, Asha Hesarghatta Shyamasunder, Rajaratnam Simon, Kapoor Nitin, Thomas Nihal, Chacko Ari |
Evaluation of Male Fertility-Associated Loci in a European Population of Patients with Severe Spermatogenic Impairment. Journal of personalized medicine 2020 Dec 11 (1): . Cerván-Martín Miriam, Bossini-Castillo Lara, Rivera-Egea Rocío, Garrido Nicolás, Luján Saturnino, Romeu Gema, Santos-Ribeiro Samuel, Ivirma Group , Lisbon Clinical Group , Castilla José A, Gonzalvo M Carmen, Clavero Ana, Vicente F Javier, Guzmán-Jiménez Andrea, Costa Cláudia, Llinares-Burguet Inés, Khantham Chiranan, Burgos Miguel, Barrionuevo Francisco J, Jiménez Rafael, Sánchez-Curbelo Josvany, López-Rodrigo Olga, Peraza M Fernanda, Pereira-Caetano Iris, Marques Patricia I, Carvalho Filipa, Barros Alberto, Bassas Lluís, Seixas Susana, Gonçalves João, Larriba Sara, Lopes Alexandra M, Palomino-Morales Rogelio J, Carmona F Dav |
TP53 mutations in functional corticotroph tumors are linked to invasion and worse clinical outcome. Acta neuropathologica communications 2022 Sep 10 (1): 139. Perez-Rivas Luis Gustavo, Simon Julia, Albani Adriana, Tang Sicheng, Roeber Sigrun, Assié Guillaume, Deutschbein Timo, Fassnacht Martin, Gadelha Monica R, Hermus Ad R, Stalla Günter K, Tichomirowa Maria A, Rotermund Roman, Flitsch Jörg, Buchfelder Michael, Nasi-Kordhishti Isabella, Honegger Jürgen, Thorsteinsdottir Jun, Saeger Wolfgang, Herms Jochen, Reincke Martin, Theodoropoulou Mari |
Ubiquitin-specific Protease 8 Gene Expression in Sporadic Pituitary Adenomas. Neuro endocrinology letters 2022 8 43 (2): 129-133. Hatipoglu Esra, Gunaldi Omur, Erkan Buruc, Avcikurt Ayla, Mert Meral, Niyazoglu Mut |
Genetics of Cushing's disease. Journal of neuroendocrinology 2022 5 34 (8): e13148. Simon Julia, Theodoropoulou Mari |
The expression of glucocorticoid and mineralocorticoid receptors in pituitary tumors causing Cushing's disease and silent corticotroph tumors. Frontiers in endocrinology 2023 4 14 1124646. Kober Paulina, Rusetska Natalia, Mossakowska Beata J, Maksymowicz Maria, P?kul Monika, Zieli?ski Grzegorz, Styk Andrzej, Kunicki Jacek, Dzia?ach ?ukasz, Witek Przemys?aw, Bujko Mateu |
Multi-ancestry genome-wide association meta-analysis of Parkinson's disease. Nature genetics 2023 12 . Jonggeol Jeffrey Kim, Dan Vitale, Diego Véliz Otani, Michelle Mulan Lian, Karl Heilbron, , Hirotaka Iwaki, Julie Lake, Caroline Warly Solsberg, Hampton Leonard, Mary B Makarious, Eng-King Tan, Andrew B Singleton, Sara Bandres-Ciga, Alastair J Noyce, , Cornelis Blauwendraat, Mike A Nalls, Jia Nee Foo, Ignacio Ma |
A long-term prognosis study of human USP8-mutated ACTH-secreting pituitary neuroendocrine tumours. Clinical endocrinology 2024 5 . Hui Miao, Luo Wang, Fengying Gong, Lian Duan, Linjie Wang, Yong Yao, Ming Feng, Kan Deng, Renzhi Wang, Yu Xiao, Qing Ling, Huijuan Zhu, Lin |
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