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

The transcription factor Tcf21 is necessary for adoption of cell fates by Foxd1(+) stromal progenitors during kidney development

转录因子Tcf21对于肾脏发育过程中Foxd1(+)基质祖细胞的细胞命运决定是必需的

期刊:
影响因子:
doi:10.1152/ajprenal.00345.2025
Finer, Gal; Yacu, George S; Khan, Mohammad Daud; Zhou, Yalu; Gadhvi, Gaurav; Ward, Sarah E; Sayed, Mohammed; Gomez, R Ariel; Sequeira-Lopez, Maria Luisa S; Park, Joo-Seop; Lim, Hee-Woong; Quaggin, Susan E; Winter, Deborah R
细胞生物学
发育与干细胞
发表日期：2026
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Tcf21 as a founder transcription factor in specifying Foxd1 cells to the juxtaglomerular cell lineage.

Tcf21 作为创始转录因子，将 Foxd1 细胞指定为肾小球旁细胞谱系

期刊:American Journal of Physiology-Renal Physiology
影响因子:3.4
doi:10.1152/ajprenal.00235.2024
Anjum Hina, Smith Jason P, Martini Alexandre G, Yacu George S, Medrano Silvia, Gomez R Ariel, Sequeira-Lopez Maria Luisa S, Quaggin Susan E, Finer Gal
细胞生物学
发表日期：2025
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Surgical Management of Pediatric Primary Hyperoxaluria Type 1: An Eight-Patient Case Series in the Pre-siRNA Era

儿童原发性高草酸尿症1型的外科治疗：siRNA时代之前的8例病例系列研究

期刊:Pediatric Transplantation
影响因子:1.4
doi:10.1111/petr.70225
Finer, Gal; Darani, Alexandre N; Switalski, Matthew G; Ward, Sarah E; Melin-Aldana, Hector; Superina, Riccardo
发表日期：2025
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Non-endothelial expression of endomucin in the mouse and human choroid.

小鼠和人类脉络膜中内皮细胞表达内皮黏蛋白

期刊:Experimental Eye Research
影响因子:2.7
doi:10.1016/j.exer.2024.110054
Brookins Elysse, Serrano Sophia E, Hyder Zain, Yacu George S, Finer Gal, Thomson Benjamin R
细胞生物学
Human
Mouse
发表日期：2024
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Renin Cell Development: Insights From Chromatin Accessibility and Single-Cell Transcriptomics

肾素细胞发育：来自染色质可及性和单细胞转录组学的启示

期刊:Circulation Research
影响因子:16.2
doi:10.1161/CIRCRESAHA.123.322827
Martini, Alexandre G; Smith, Jason P; Medrano, Silvia; Finer, Gal; Sheffield, Nathan C; Sequeira-Lopez, Maria Luisa S; Gomez, R Ariel
细胞生物学
发育与干细胞
单细胞
发表日期：2023
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A conceptual framework for the molecular pathogenesis of progressive kidney disease

进行性肾病分子发病机制的概念框架

期刊:Pediatric Nephrology
影响因子:2.6
doi:10.1007/s00467-010-1503-4
Schnaper, H William; Hubchak, Susan C; Runyan, Constance E; Browne, James A; Finer, Gal; Liu, Xiaoying; Hayashida, Tomoko
发表日期：2010
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Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9

由基因组印记钾通道KCNK9基因突变引起的母系遗传性Birk-Barel智力低下畸形综合征

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2008.07.010
Barel, Ortal; Shalev, Stavit A; Ofir, Rivka; Cohen, Asi; Zlotogora, Joel; Shorer, Zamir; Mazor, Galia; Finer, Gal; Khateeb, Shareef; Zilberberg, Noam; Birk, Ohad S
发表日期：2008
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Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQ

线粒体复合物 III 缺陷与 UQCRQ 基因纯合突变相关

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2008.03.020
Barel, Ortal; Shorer, Zamir; Flusser, Hagit; Ofir, Rivka; Narkis, Ginat; Finer, Gal; Shalev, Hanah; Nasasra, Ahmad; Saada, Ann; Birk, Ohad S
线粒体
发表日期：2008
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