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

Impact of aging on gene expression in human oocytes: a comparative analysis of young and older patients

衰老对人类卵母细胞基因表达的影响:年轻患者与老年患者的比较分析

Orvieto, Raoul; Nayshool, Omri; Cohen, Louisa; Yung, Yuval; Aizer, Adva; Saar, Efrat Glick; Dominissini, Dan

Curcumin-QingDai combination for patients with active Crohn's disease: a retrospective, real-world multicenter cohort study

姜黄素-青岛联合疗法治疗活动性克罗恩病患者:一项回顾性、真实世界多中心队列研究

Salomon, Nir; Marom, Maayan; Odeh, Safwat; Molnar, Madlen; Shitrit, Ariella Bar-Gil; Nayshool, Omri; Ungar, Bella; Ben-Horin, Shomron; Rainis, Tova

SurviveAI: Long Term Survival Prediction of Cancer Patients Based on Somatic RNA-Seq Expression

SurviveAI:基于体细胞RNA测序表达的癌症患者长期生存预测

Nayshool, Omri; Kol, Nitzan; Javaski, Elisheva; Amariglio, Ninette; Rechavi, Gideon

A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies

单中心利用公共资金进行临床外显子组测序以诊断神经发育障碍或多发性先天性异常的经验

Pode-Shakked, Ben; Barel, Ortal; Singer, Amihood; Regev, Miriam; Poran, Hana; Eliyahu, Aviva; Finezilber, Yael; Segev, Meirav; Berkenstadt, Michal; Yonath, Hagith; Reznik-Wolf, Haike; Gazit, Yael; Chorin, Odelia; Heimer, Gali; Gabis, Lidia V; Tzadok, Michal; Nissenkorn, Andreea; Bar-Yosef, Omer; Zohar-Dayan, Efrat; Ben-Zeev, Bruria; Mor, Nofar; Kol, Nitzan; Nayshool, Omri; Shimshoviz, Noam; Bar-Joseph, Ifat; Marek-Yagel, Dina; Javasky, Elisheva; Einy, Reviva; Gal, Moran; Grinshpun-Cohen, Julia; Shohat, Mordechai; Dominissini, Dan; Raas-Rothschild, Annick; Rechavi, Gideon; Pras, Elon; Greenbaum, Lior

High frequency of C9orf72 hexanucleotide repeat expansion in amyotrophic lateral sclerosis patients from two founder populations sharing the same risk haplotype

在两个具有相同风险单倍型的创始人群中,肌萎缩侧索硬化症患者中C9orf72六核苷酸重复扩增的频率很高

Goldstein, Orly; Gana-Weisz, Mali; Nefussy, Beatrice; Vainer, Batel; Nayshool, Omri; Bar-Shira, Anat; Traynor, Bryan J; Drory, Vivian E; Orr-Urtreger, Avi

OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes

OPTN 691_692insAG 是一种创始突变,会导致隐性遗传的 ALS,并且会增加杂合子患病的风险。

Goldstein, Orly; Nayshool, Omri; Nefussy, Beatrice; Traynor, Bryan J; Renton, Alan E; Gana-Weisz, Mali; Drory, Vivian E; Orr-Urtreger, Avi

Cellularized biosynthetic microhydrogel polymers for intravascular liver tissue regeneration therapy

用于血管内肝组织再生治疗的细胞化生物合成微水凝胶聚合物

Saadi, Tarek; Nayshool, Omri; Carmel, Julie; Ariche, Arie; Bramnik, Zakhar; Mironi-Harpaz, Iris; Seliktar, Dror; Baruch, Yaacov