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

A Novel Frameshift Variant and a Partial EHMT1 Microdeletion in Kleefstra Syndrome 1 Patients Resulting in Variable Phenotypic Severity and Literature Review

克利夫斯特拉综合征1型患者中一种新的移码变异和EHMT1部分微缺失导致表型严重程度差异及文献综述

Tzetis, Maria; Mitrakos, Anastasios; Papathanasiou, Ioanna; Koute, Vasiliki; Kosma, Konstantina; Pons, Roser; Michoula, Aspasia; Grivea, Ioanna; Tsezou, Aspasia

Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome

对 EHMT1 变异体的全面分析拓宽了 Kleefstra 综合征的基因型-表型关联和分子机制。

Rots, Dmitrijs; Bouman, Arianne; Yamada, Ayumi; Levy, Michael; Dingemans, Alexander J M; de Vries, Bert B A; Ruiterkamp-Versteeg, Martina; de Leeuw, Nicole; Ockeloen, Charlotte W; Pfundt, Rolph; de Boer, Elke; Kummeling, Joost; van Bon, Bregje; van Bokhoven, Hans; Kasri, Nael Nadif; Venselaar, Hanka; Alders, Marielle; Kerkhof, Jennifer; McConkey, Haley; Kuechler, Alma; Elffers, Bart; van Beeck Calkoen, Rixje; Hofman, Susanna; Smith, Audrey; Valenzuela, Maria Irene; Srivastava, Siddharth; Frazier, Zoe; Maystadt, Isabelle; Piscopo, Carmelo; Merla, Giuseppe; Balasubramanian, Meena; Santen, Gijs W E; Metcalfe, Kay; Park, Soo-Mi; Pasquier, Laurent; Banka, Siddharth; Donnai, Dian; Weisberg, Daniel; Strobl-Wildemann, Gertrud; Wagemans, Annemieke; Vreeburg, Maaike; Baralle, Diana; Foulds, Nicola; Scurr, Ingrid; Brunetti-Pierri, Nicola; van Hagen, Johanna M; Bijlsma, Emilia K; Hakonen, Anna H; Courage, Carolina; Genevieve, David; Pinson, Lucile; Forzano, Francesca; Deshpande, Charu; Kluskens, Maria L; Welling, Lindsey; Plomp, Astrid S; Vanhoutte, Els K; Kalsner, Louisa; Hol, Janna A; Putoux, Audrey; Lazier, Johanna; Vasudevan, Pradeep; Ames, Elizabeth; O'Shea, Jessica; Lederer, Damien; Fleischer, Julie; O'Connor, Mary; Pauly, Melissa; Vasileiou, Georgia; Reis, André; Kiraly-Borri, Catherine; Bouman, Arjan; Barnett, Chris; Nezarati, Marjan; Borch, Lauren; Beunders, Gea; Özcan, Kübra; Miot, Stéphanie; Volker-Touw, Catharina M L; van Gassen, Koen L I; Cappuccio, Gerarda; Janssens, Katrien; Mor, Nofar; Shomer, Inna; Dominissini, Dan; Tedder, Matthew L; Muir, Alison M; Sadikovic, Bekim; Brunner, Han G; Vissers, Lisenka E L M; Shinkai, Yoichi; Kleefstra, Tjitske

A multi-layered computational structural genomics approach enhances domain-specific interpretation of Kleefstra syndrome variants in EHMT1

多层计算结构基因组学方法增强了对 EHMT1 中 Kleefstra 综合征变异的结构域特异性解读

Chi, Young-In; Jorge, Salomão D; Jensen, Davin R; Smith, Brian C; Volkman, Brian F; Mathison, Angela J; Lomberk, Gwen; Zimmermann, Michael T; Urrutia, Raul

Tourette-like syndrome secondary to Kleefstra syndrome 1 with a de novo microdeletion in the EHMT1 gene

继发于 Kleefstra 综合征 1 的 Tourette 样综合征,伴有 EHMT1 基因的新发微缺失

Niu, Mengyue; Li, Yanjing; Zhan, Shikun; Sun, Bomin; Liu, Jun; Wu, Yiwen

Reanalysis of Chromosomal Microarray Data Using a Smaller Copy Number Variant Call Threshold Identifies Four Cases with Heterozygous Multiexon Deletions of ARID1B, EHMT1, and FOXP1 Genes

利用更小的拷贝数变异阈值对染色体微阵列数据进行重新分析,发现了四例ARID1B、EHMT1和FOXP1基因杂合多外显子缺失病例。

Kubota, Noriko; Takeda, Ryojun; Kobayashi, Jun; Hidaka, Eiko; Nishi, Eriko; Takano, Kyoko; Wakui, Keiko

Combinatory EHMT and PARP inhibition induces an interferon response and a CD8 T cell-dependent tumor regression in PARP inhibitor-resistant models

EHMT 和 PARP 联合抑制可在 PARP 抑制剂耐药模型中诱导干扰素反应和 CD8 T 细胞依赖性肿瘤消退

Lily L Nguyen, Zachary L Watson, Raquel Ortega, Elizabeth R Woodruff, Kimberly R Jordan, Ritsuko Iwanaga, Tomomi M Yamamoto, Courtney A Bailey, Abigail D Jeong, Saketh R Guntupalli, Kian Behbakht, Veronica Gbaja, Nausica Arnoult, Edward B Chuong, Benjamin G Bitler

A Multi-Layered Computational Structural Genomics Approach Enhances Domain-Specific Interpretation of Kleefstra Syndrome Variants in EHMT1

多层计算结构基因组学方法增强了对 EHMT1 中 Kleefstra 综合征变异的结构域特异性解读

Chi, Young-In; Jorge, Salomão D; Jensen, Davin R; Smith, Brian C; Volkman, Brian F; Mathison, Angela J; Lomberk, Gwen; Zimmermann, Michael T; Urrutia, Raul

Potential Therapeutics Targeting Upstream Regulators and Interactors of EHMT1/2

针对 EHMT1/2 上游调控因子和相互作用因子的潜在治疗方法

Ang, Gareth Chin Khye; Gupta, Amogh; Surana, Uttam; Yap, Shirlyn Xue Ling; Taneja, Reshma

Epigenetic Silencing of CHOP Expression by the Histone Methyltransferase EHMT1 Regulates Apoptosis in Colorectal Cancer Cells

组蛋白甲基转移酶 EHMT1 的表观遗传沉默 CHOP 表达可调控结直肠癌细胞凋亡

Kwangho Kim, Tae Young Ryu, Jinkwon Lee, Mi-Young Son, Dae-Soo Kim, Sang Kyum Kim, Hyun-Soo Cho

SPOP mutation induces DNA methylation via stabilizing GLP/G9a

SPOP 突变通过稳定 GLP/G9a 诱导 DNA 甲基化

Jianong Zhang, Kun Gao, Hongyan Xie, Dejie Wang, Pingzhao Zhang, Ting Wei, Yuqian Yan, Yunqian Pan, Wenbin Ye, Huifen Chen, Qing Shi, Yao Li, Shi-Min Zhao, Xiaonan Hou, Saravut J Weroha, Yuzhuo Wang, Jun Zhang, R Jeffrey Karnes, Housheng Hansen He, Liguo Wang, Chenji Wang, Haojie Huang