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

Genetic Terminal Complement Deficiency in Israeli Bedouins With Kidney Failure

以色列贝都因人肾衰竭中的遗传性末端补体缺陷

Chowers, Guy; Ben-Ruby, Dror; Atias-Varon, Danit; Shlomovitz, Omer; Slabodnik-Kaner, Keren; Kagan, Maayan; Avayou, Shany; Romanjuk, Elvira; Rogachev, Boris; Haviv, Yosef S; Birk, Ohad S; Hadar, Noam; Bathish, Younes; Barshack, Iris; Volkov, Alexander; Avivi, Camila; Pavlovsky, Anna; Haskin, Orly; Simon, Amos J; Glick-Saar, Efrat; Ostrovsky, Alina; Assi, Mawada; Schreiber, Ruth; Levin, Dana; Yagil, Yoram; Awawdeh, Mohammad; Skorecki, Karl; Dominissini, Dan; Shnaider, Alla; Vivante, Asaf

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

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

Targeting bladder cancer: Potent anti-cancer effects of cannabichromene and delta-9-tetrahydrocannabinol-rich Cannabis sativa strains

针对膀胱癌:富含大麻色烯和Δ-9-四氢大麻酚的大麻品种具有强大的抗癌作用

Anis, Omer; Bar, Vered; Zundelevich, Adi; Anil, Seegehali M; Shav-Tal, Yaron; Toren, Amos; Dominissini, Dan; Raviv, Gil; Laufer, Menachem; Lazarovich, Alon; Drori, Tomer; Ramon, Jacob; Dotan, Zohar; Koltai, Hinanit

Small Extracellular Vesicles From Infarcted and Failing Heart Accelerate Tumor Growth

梗死和衰竭心脏产生的小型细胞外囊泡加速肿瘤生长

Caller, Tal; Rotem, Itai; Shaihov-Teper, Olga; Lendengolts, Daria; Schary, Yeshai; Shai, Ruty; Glick-Saar, Efrat; Dominissini, Dan; Motiei, Menachem; Katzir, Idan; Popovtzer, Rachela; Nahmoud, Merav; Boomgarden, Alex; D'Souza-Schorey, Crislyn; Naftali-Shani, Nili; Leor, Jonathan

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

Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features

以色列Ser77Tyr转甲状腺素蛋白淀粉样变性:早期表现和诊断特征

Dori, Amir; Arad, Michael; Wasserstrum, Yishay; Pollak, Arthur; Nikitin, Vera; Ben-David, Merav; Shamash, Jana; Nahum, Ayelet Hashachar; Shavit-Stein, Efrat; Domachevsky, Liran; Kuperstein, Rafael; Dominissini, Dan; Shelestovich, Natalia; Sadeh, Menachem; Pras, Elon; Greenbaum, Lior

Early and late manifestations of neuropathy due to HSPB1 mutation in the Jewish Iranian population

犹太伊朗人群中由 HSPB1 基因突变引起的神经病变的早期和晚期表现

Greenbaum, Lior; Ben-David, Merav; Nikitin, Vera; Gera, Orna; Barel, Ortal; Hersalis-Eldar, Adi; Shamash, Jana; Shimshoviz, Noam; Reznik-Wolf, Haike; Shohat, Mordechai; Dominissini, Dan; Pras, Elon; Dori, Amir

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

Single base resolution mapping of 2'-O-methylation sites in human mRNA and in 3' terminal ends of small RNAs

人类mRNA和小RNA 3'末端2'-O-甲基化位点的单碱基分辨率定位

Hsu, Phillip J; Fei, Qili; Dai, Qing; Shi, Hailing; Dominissini, Dan; Ma, Lijia; He, Chuan