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

PD-1 Blockade-Induced DKK1 Expression by CD8+ T Cells Promotes Blood-Brain Barrier Permeabilization

PD-1阻断诱导的CD8+ T细胞DKK1表达促进血脑屏障通透性增加

Deo, Abhilash; Levin, Sapir; Buxbaum, Chen; Benguigui, Madeleine; Manobla, Bar; Saar, Galit; Bosak, Noam; Bergmann, Eyal; Eran, Ayelet; Grinfeld, Anat; Harel, Michal; Lahav, Coren; Raviv, Ziv; Daher, Sameh; Zer, Alona; Reuter, Julia Helena; Heuβel, Claus Peter; Christopoulos, Petros; Yizhak, Keren; Shaked, Yuval

Biallelic PIGM Coding Variant Causes Intractable Epilepsy and Intellectual Disability Without Thrombotic Events

双等位基因PIGM编码变异导致难治性癫痫和智力障碍,但无血栓事件

Heimer, Gali; Pode-Shakked, Ben; Marek-Yagel, Dina; Vernitsky, Helly; Tzadok, Michal; Barel, Ortal; Eyal, Eran; Ben-Zeev, Bruria; Atzmon, Gil; Anikster, Yair

OffRisk: a docker image for annotating CRISPR off-target sites in the human genome

OffRisk:用于注释人类基因组中 CRISPR 脱靶位点的 Docker 镜像

Barkai, Gil-Ad; Malul, Tal; Eliaz, Yossi; Eyal, Eran; Veksler-Lublinsky, Isana

ESR1 mutations are frequent in newly diagnosed metastatic and loco-regional recurrence of endocrine-treated breast cancer and carry worse prognosis

ESR1 突变在接受内分泌治疗的乳腺癌新诊断的转移性和局部区域复发病例中很常见,且预后较差。

Zundelevich, Adi; Dadiani, Maya; Kahana-Edwin, Smadar; Itay, Amit; Sella, Tal; Gadot, Moran; Cesarkas, Karen; Farage-Barhom, Sarit; Saar, Efrat Glick; Eyal, Eran; Kol, Nitzan; Pavlovski, Anya; Balint-Lahat, Nora; Dick-Necula, Daniela; Barshack, Iris; Kaufman, Bella; Gal-Yam, Einav Nili

Whole-genome sequencing reveals principles of brain retrotransposition in neurodevelopmental disorders

全基因组测序揭示了神经发育障碍中脑逆转录转座的原理

Jacob-Hirsch, Jasmine; Eyal, Eran; Knisbacher, Binyamin A; Roth, Jonathan; Cesarkas, Karen; Dor, Chen; Farage-Barhom, Sarit; Kunik, Vered; Simon, Amos J; Gal, Moran; Yalon, Michal; Moshitch-Moshkovitz, Sharon; Tearle, Rick; Constantini, Shlomi; Levanon, Erez Y; Amariglio, Ninette; Rechavi, Gideon

Congenital protein losing enteropathy: an inborn error of lipid metabolism due to DGAT1 mutations.

先天性蛋白丢失性肠病:一种由 DGAT1 基因突变引起的先天性脂质代谢异常

Stephen Joshi, Vilboux Thierry, Haberman Yael, Pri-Chen Hadass, Pode-Shakked Ben, Mazaheri Sina, Marek-Yagel Dina, Barel Ortal, Di Segni Ayelet, Eyal Eran, Hout-Siloni Goni, Lahad Avishay, Shalem Tzippora, Rechavi Gideon, Malicdan May Christine V, Weiss Batia, Gahl William A, Anikster Yair

G23D: Online tool for mapping and visualization of genomic variants on 3D protein structures

G23D:用于在三维蛋白质结构上映射和可视化基因组变异的在线工具

Solomon, Oz; Kunik, Vered; Simon, Amos; Kol, Nitzan; Barel, Ortal; Lev, Atar; Amariglio, Ninette; Somech, Raz; Rechavi, Gidi; Eyal, Eran

High metallothionein predicts poor survival in glioblastoma multiforme

高金属硫蛋白水平预示着多形性胶质母细胞瘤患者生存率低

Mehrian-Shai, Ruty; Yalon, Michal; Simon, Amos J; Eyal, Eran; Pismenyuk, Tatyana; Moshe, Itai; Constantini, Shlomi; Toren, Amos

Global regulation of alternative splicing by adenosine deaminase acting on RNA (ADAR)

腺苷脱氨酶作用于RNA(ADAR)对选择性剪接进行全局调控

Solomon, Oz; Oren, Shirley; Safran, Michal; Deshet-Unger, Naamit; Akiva, Pinchas; Jacob-Hirsch, Jasmine; Cesarkas, Karen; Kabesa, Reut; Amariglio, Ninette; Unger, Ron; Rechavi, Gideon; Eyal, Eran

Mutagen-specific mutation signature determines global microRNA binding

诱变剂特异性突变特征决定了整体microRNA结合

Greenberg, Eyal; Rechavi, Gideon; Amariglio, Ninette; Solomon, Oz; Schachter, Jacob; Markel, Gal; Eyal, Eran