日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Further Exploring the TRRAP Genotype-Phenotype Correlations: Report of Three New Patients With A Focus on Skeletal Anomalies

进一步探索TRRAP基因型-表型相关性:三例新患者的报告,重点关注骨骼异常

Minotti, Chiara; Terreri, Sara; Del Fattore, Andrea; Lepri, Francesca Romana; Ruta, Rosario; Iascone, Maria; Pezzoli, Laura; Dentici, Maria Lisa; Novelli, Antonio; Armando, Michelina; Longo, Daniela; Novelli, Giuseppe; Barbuti, Domenico; Bartuli, Andrea; Cavallari, Ugo; Graziani, Ludovico; Digilio, Maria Cristina; Sinibaldi, Lorenzo

Novel Pathogenic Variant of the TRRAP Gene Detected in a Hungarian Family with Autosomal Dominant Non-Syndromic Hearing Loss

在匈牙利一个患有常染色体显性非综合征性听力损失的家族中检测到TRRAP基因的新型致病变异

Nagy, Nikoletta; Szalenko-Tőkés, Ágnes; Pál, Margit; Bokor, Barbara Anna; Nagy, Roland; Jarabin, János András; Róvó, László; Széll, Márta

Interaction of transcription factor FoxO3 with histone acetyltransferase complex subunit TRRAP modulates gene expression and apoptosis

转录因子FoxO3与组蛋白乙酰转移酶复合物亚基TRRAP的相互作用调节基因表达和细胞凋亡

Lorenza Fusi ,Rupesh Paudel ,Katharina Meder ,Andreas Schlosser ,David Schrama ,Matthias Goebeler ,Marc Schmidt

S146L in MYC is a context-dependent activating substitution in cancer development

MYC基因中的S146L突变是癌症发展过程中一种依赖于特定环境的激活突变。

John W Hinds ,Edmond J Feris ,Owen M Wilkins ,Luke T Deary ,Xiaofeng Wang ,Michael D Cole

HAT cofactor TRRAP modulates microtubule dynamics via SP1 signaling to prevent neurodegeneration

HAT 辅因子 TRRAP 通过 SP1 信号通路调节微管动力学,从而预防神经退行性变。

Alicia Tapias # ,David Lázaro # ,Bo-Kun Yin # ,Seyed Mohammad Mahdi Rasa ,Anna Krepelova ,Erika Kelmer Sacramento ,Paulius Grigaravicius ,Philipp Koch ,Joanna Kirkpatrick ,Alessandro Ori ,Francesco Neri ,Zhao-Qi Wang

Luminescence complementation technology for the identification of MYC:TRRAP inhibitors

发光互补技术用于鉴定MYC:TRRAP抑制剂

Edmond J Feris, John W Hinds, Michael D Cole

Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability

组蛋白乙酰转移酶复合物组分基因TRRAP的错义变异会导致自闭症和综合征型智力障碍

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 M

TRRAP is a central regulator of human multiciliated cell formation

TRRAP是人类多纤毛细胞形成的核心调节因子

Zhao Wang ,Lindsey W Plasschaert ,Shivani Aryal ,Nicole A Renaud ,Zinger Yang ,Rayman Choo-Wing ,Angelica D Pessotti ,Nathaniel D Kirkpatrick ,Nadire R Cochran ,Walter Carbone ,Rob Maher ,Alicia Lindeman ,Carsten Russ ,John Reece-Hoyes ,Gregory McAllister ,Gregory R Hoffman ,Guglielmo Roma ,Aron B Jaffe

TRRAP stimulates the tumorigenic potential of ovarian cancer stem cells

TRRAP刺激卵巢癌干细胞的致瘤潜能

Kang, Kyung Taek; Kwon, Yang Woo; Kim, Dae Kyoung; Lee, Su In; Kim, Ki-Hyung; Suh, Dong-Soo; Kim, Jae Ho

De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case report

一例伴有非语言学习障碍和强迫症的极早期精神病患者,其TRRAP基因存在新生变异:病例报告

Mavros, Chrystal F; Brownstein, Catherine A; Thyagrajan, Roshni; Genetti, Casie A; Tembulkar, Sahil; Graber, Kelsey; Murphy, Quinn; Cabral, Kristin; VanNoy, Grace E; Bainbridge, Matthew; Shi, Jiahai; Agrawal, Pankaj B; Beggs, Alan H; D'Angelo, Eugene; Gonzalez-Heydrich, Joseph