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

Serum renin levels refine acute kidney injury prediction in critically ill children

血清肾素水平可提高危重儿童急性肾损伤的预测准确性

Pode-Shakked, Naomi; Ceschia, Giovanni; Rose, James E; Krallman, Kelli A; Goldstein, Stuart L; Stanski, Natalja L

Impact of Growth Hormone Treatment in Children From an Extended Family With ACAN -Related Short Stature

生长激素治疗对患有ACAN相关矮小症的大家庭儿童的影响

Shalev-Goldman, Einat; Asaly, Ayman; Ityel, Hadas; Pode-Shakked, Ben; Modan-Moses, Dalit; Levy-Shraga, Yael

Detection of the Heterozygous Recurrent MAX p.(Arg60Gln) Variant in Two Females Confirms and Expands the Phenotypic Spectrum of Polydactyly-Macrocephaly Syndrome

在两名女性中检测到杂合复发性 MAX p.(Arg60Gln) 变异,证实并扩展了多指-巨头综合征的表型谱。

Showpnil, Iftekhar A; Feinstein-Goren, Neta; Greenbaum, Lior; Barel, Ortal; Koboldt, Daniel C; Brugmann, Samantha A; Weaver, Kathryn Nicole; Slavotinek, Anne; Pode-Shakked, Ben; Stottmann, Rolf W

Integrating collecting systems in human kidney organoids through fusion of distal nephron to ureteric bud.

通过将远端肾单位与输尿管芽融合,在人类肾脏类器官中整合集合系统

Shi Min, Crouse Brittney, Sundaram Nambirajan, Pode Shakked Naomi, Thorner Konrad, King Nathaniel M, Dutta Parna, Ester Lioba, Zhang Weitao, Govindarajah Vinothini, Kopan Raphael, Cebrian Cristina, Mayhew Christopher N, Helmrath Michael A, Bonventre Joseph V, McCracken Kyle W

Human fetal kidney organoids model early human nephrogenesis and Notch-driven cell fate

人类胎儿肾脏类器官模拟早期人类肾脏发育和Notch信号通路驱动的细胞命运

Michael Namestnikov ,Osnat Cohen-Zontag ,Dorit Omer ,Yehudit Gnatek ,Sanja Goldberg ,Thomas Vincent ,Swati Singh ,Yair Shiber ,Tal Rafaeli Yehudai ,Hadas Volkov ,Dani Folkman Genet ,Achia Urbach ,Sylvie Polak-Charcon ,Igor Grinberg ,Naomi Pode-Shakked ,Boaz Weisz ,Zvi Vaknin ,Benjamin S Freedman ,Benjamin Dekel

A novel Frizzled 7 antibody disrupts the Wnt pathway and inhibits Wilms tumor growth

一种新型的Frizzled 7抗体可干扰Wnt信号通路并抑制Wilms肿瘤的生长。

Vax, Einav; Caspi, Revital; Shukrun, Rachel; Pode-Shakked, Naomi; Pleniceanu, Oren; Golan, Hana; Namestnikov, Michael; Mark-Danieli, Michal; Markovsky, Ela; Bar-Lev, Dekel D; Barshack, Iris; Satchi-Fainaro, Ronit; Harari-Steinberg, Orit; Goldberg, Sanja; Dekel, Benjamin

OSR1 and SIX2 drive divergent transcriptional programs in human kidney cells: implications for regeneration and tumorigenesis

OSR1和SIX2在人类肾细胞中驱动不同的转录程序:对再生和肿瘤发生的影响

Pode-Shakked, Naomi; Cohen-Zontag, Osnat; Omer, Dorit; Harari-Steinberg, Orit; Vax, Einav; Pleniceanu, Oren; Dekel, Benjamin

Clinical profiling and medical management of Israeli individuals with Phelan McDermid syndrome

对患有费兰-麦克德米德综合征的以色列患者进行临床特征分析和医疗管理

Chorin, Odelia; Greenbaum, Lior; Lev-Hochberg, Shelly; Feinstein-Goren, Neta; Eliyahu, Aviva; Shani, Hagit; Pras, Elon; Weissbach, Tal; Bolkier, Yoav; Heimer, Gali; Lev, Dorit; Michelson, Marina; Regev, Miriam; Josefsberg, Sagi; Batzir, Nurit Assia; Shalata, Adel; Spiegel, Ronen; Segel, Reeval; Lobel, Orit; Abu-Libdeh, Bassam; Shohat, Mordechai; Frydman, Moshe; Hady-Cohen, Ronen; Pode-Shakked, Ben; Rein-Rothschild, Annick

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

GRID1/GluD1 homozygous variants linked to intellectual disability and spastic paraplegia impair mGlu1/5 receptor signaling and excitatory synapses

与智力障碍和痉挛性截瘫相关的GRID1/GluD1纯合变异会损害mGlu1/5受体信号传导和兴奋性突触。

Ung, Dévina C; Pietrancosta, Nicolas; Badillo, Elena Baz; Raux, Brigitt; Tapken, Daniel; Zlatanovic, Andjela; Doridant, Adrien; Pode-Shakked, Ben; Raas-Rothschild, Annick; Elpeleg, Orly; Abu-Libdeh, Bassam; Hamed, Nasrin; Papon, Marie-Amélie; Marouillat, Sylviane; Thépault, Rose-Anne; Stevanin, Giovanni; Elegheert, Jonathan; Letellier, Mathieu; Hollmann, Michael; Lambolez, Bertrand; Tricoire, Ludovic; Toutain, Annick; Hepp, Régine; Laumonnier, Frédéric