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

Genotoxic carcinogenicity of pyrrolizidine alkaloids: relevance of potency factors for the risk assessment

吡咯里西啶生物碱的遗传毒性致癌性:效力因子对风险评估的相关性

Sachse, Benjamin; Hessel-Pras, Stefanie; Schäfer, Bernd

The Genetic Landscape of Inherited Retinal Diseases in the Israeli Population

以色列人群遗传性视网膜疾病的遗传图谱

Shalom, Sapir; Gradstein, Libe; Pras, Eran; Valensi, Johanna; Birk, Ohad S; Blumenfeld, Anat; Eilat, Avital; Macarov, Michal; Poleg, Tomer; Cremers, Frans P M; Roosing, Susanne; Panneman, Daan M; Hollander, Nadin; Goldenberg-Cohen, Nitza; Yahalom, Claudia; Banin, Eyal; Ben-Yosef, Tamar; Sharon, Dror

Broadening the Phenotypic Spectrum of MAFB-Related Disease: Renal, Auricular, Ocular, and Nervous System Involvement

扩大MAFB相关疾病的表型谱:肾脏、耳部、眼部和神经系统受累

Eliyahu, Aviva; Atias-Varon, Danit; Barel, Ortal; Khavkin, Yulia; Pras, Elon; Reznik-Wolf, Haike; Chorin, Odelia; Poleg, Tomer; Biller, Ari; Beckerman, Pazit; Abu-Amer, Nabil; Wygnanski-Jaffe, Tamara; Greenbaum, Lior; Vivante, Asaf; Krause, Irit

HEPES in Cell Culture Alters the Multi-Omics Profile Exhibited by Gaucher Disease Fibroblasts

HEPES在细胞培养中改变了戈谢病成纤维细胞的多组学特征

Corazolla, Eleonore M; Schomakers, Bauke V; Trętowicz, Maria M; Hermans, Jill; van Weeghel, Michel; Vaz, Frédéric M; Pras-Raves, Mia L; Vlugt, Karen Ghauharali-van der; Beers-Stet, Femke S; Goorden, Susanna M I; Jansen-Meijer, Judith; Janssens, Georges E; Hollak, Carla E M; Houtkooper, Riekelt H; van Kuilenburg, André B P

Evaluation of the digital genetic assistant in technology assisted genetic counseling for genetic carrier screening

对数字基因助手在基因携带者筛查技术辅助遗传咨询中的应用进行评估

Yaron, Yuval; Ofen Glassner, Vered; Berkenstadt, Michal; Goldstein, Nurit; Reznik Wolf, Haike; Ries Levavi, Liat; Abo Gutstein, Liat; Furman, Yael; Anouchi, Mori; Delmar, Galit; Behar, Doron M; Pras, Elon; Reches, Adi; Kurolap, Alina; Baris Feldman, Hagit

The pyrrolizidine alkaloid lasiocarpine impairs cell cycle progression in vitro

吡咯里西啶生物碱拉西卡品在体外会抑制细胞周期进程。

Hessel-Pras, Stefanie; Beckschulte, Marlena; Peters, Antonia; Koellner, Anja; Rosskopp, Beatrice; Stahl, Aaron; Templin, Markus; Sprenger, Heike; Boehmert, Linda; Kuepper, Jan-Heiner; Sachse, Benjamin; Schaefer, Bernd

Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy.

C19orf44 中的双等位基因无效变异会导致一种独特的迟发性视网膜营养不良表型,其特征是斑片状中心凹周围脉络膜视网膜萎缩

Ehrenberg Miriam, Avraham Maayan, Asodu Sandeep Sarma, Moye Abigail R, Sangermano Riccardo, Rizel Leah, Ali-Nasser Tahleel, Sher Ifat, Gurwitz David, Chao Katherine R, Rivera Antonio, Webster Andrew R, Rivolta Carlo, Newman Hadas, Pras Eran, Rotenstreich Ygal, Banin Eyal, Pierce Eric A, Zur Dinah, Arno Gavin, Bujakowska Kinga M, Lin Siying, Sharon Dror, Ben-Yosef Tamar

Vasculitis as an indicator of disease severity in familial Mediterranean fever

血管炎是家族性地中海热疾病严重程度的指标

Barzilai, Aviv; Mash, Yarin; Gershon, Rotem; Pras, Elon; Baum, Sharon

Preclinical Validation of a Patient-Specific Patch-Planning Workflow for Congenital Cardiovascular Reconstruction

先天性心血管重建患者特异性补片规划工作流程的临床前验证

Kizilski, Shannen B; Recco, Dominic P; Davee, Jocelyn M; Masterson, Ashley; Yao, Jiang; Earley, Patrick D; Kneier, Nicholas E; Aycock, Kenneth I; Craven, Brent A; Pathmanathan, Pras; Hammer, Peter E; Hoganson, David M

Multiethnic prevalence of the APOL1 G1 and G2 variants among the Israeli dialysis population.

以色列透析人群中 APOL1 G1 和 G2 变体的多民族患病率

Ben-Ruby Dror, Atias-Varon Danit, Kagan Maayan, Chowers Guy, Shlomovitz Omer, Slabodnik-Kaner Keren, Mano Neta, Avayou Shany, Atsmony Yariv, Levin Dana, Dotan Edo, Calderon-Margalit Ronit, Shnaider Alla, Haviv Yosef S, Birk Ohad S, Hadar Noam, Anikster Yair, Berar Yanay Noa, Chernin Gil, Kruzel-Davila Etty, Beckerman Pazit, Rozen-Zvi Benaya, Doctor Gabriel T, Stanescu Horia C, Shemer Revital, Pras Elon, Reznik-Wolf Haike, Nahum Ayelet Hashahar, Dominissini Dan, Skorecki Karl, Vivante Asaf