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

Acute kidney injury due to diarrhoeal diseases in children: a systematic review

儿童腹泻性疾病引起的急性肾损伤:系统评价

Merz, Lea M; Kamath, Nivedita; Adetunji, Adewale E; Luyckx, Valerie A

Exome Sequencing in Saudi Arabian Pediatric Kidney Disease Single-Center Cohort

沙特阿拉伯儿童肾脏疾病单中心队列的外显子组测序

Lemberg, Katharina; Shalaby, Mohamed A; Zion, Elena; Saida, Ken; Yousef, Kirollos; Schneider, Ronen; Mertens, Nils D; Mansour, Bshara; Kolvenbach, Caroline M; Merz, Lea M; Riedhammer, Korbinian M; Braun, Alina; Hölzel, Selina; Yu, Seyoung; Lomjansook, Kraisoon; Kalkar, Gina; Marchuk, Daniel; Elmubarak, Izzeldin; Franken, Gijs A C; Shril, Shirlee; El Desoky, Sherif; Kari, Jameela A; Buerger, Florian; Hildebrandt, Friedhelm

Effects of alpelisib treatment on murine Pten-deficient lipomas.

alpelisib治疗对小鼠Pten缺陷型脂肪瘤的影响

Merz Lea M, Winter Karsten, Richter Sandy, Kallendrusch Sonja, Horn Andreas, Grunewald Sonja, Klöting Nora, Krause Kerstin, Kiess Wieland, Le Duc Diana, Garten Antje

Phenotypic quantification of Nphs1-deficient mice

Nphs1缺陷小鼠的表型定量分析

Schneider, Ronen; Mansour, Bshara; Kolvenbach, Caroline M; Buerger, Florian; Salmanullah, Daanya; Lemberg, Katharina; Merz, Lea M; Mertens, Nils D; Saida, Ken; Yousef, Kirollos; Franken, Gijs A C; Bao, Aaron; Yu, Seyoung; Hölzel, Selina; Nicolas-Frank, Camille; Steinsapir, Andrew; Goncalves, Kevin A; Shril, Shirlee; Hildebrandt, Friedhelm

CAKUT variants in PRPF8, DYRK2, and CEP78: implications for splicing and ciliogenesis

PRPF8、DYRK2 和 CEP78 中的 CAKUT 变异:对剪接和纤毛发生的影响

Merz, Lea M; Shril, Shirlee; Carrocci, Tucker J; Rezi, Csenge K; Zeps, Natalie J; Jiménez-Izquierdo, Rafael; Bergmann, Florian; Petriman, Narcis Adrian; Kolvenbach, Caroline M; Mertens, Nils D; Johansen, Søren L; Halbritter, Jan; Hilger, Alina Christine; Mohiuddin, Shaikh Qureshi Wasay; Hentges, Kathryn E; Rasouly, Hila Milo; Gharavi, Ali G; Yoshida, Kiyotsugu; Lorentzen, Esben; Calzado, Marco; Kispert, Andreas; Yoshida, Saishu; Pedersen, Lotte B; Hoskins, Aaron A; Buerger, Florian; Hildebrandt, Friedhelm

Quantifiable and reproducible phenotypic assessment of a constitutive knockout mouse model for congenital nephrotic syndrome of the Finnish type.

对芬兰型先天性肾病综合征的组成型基因敲除小鼠模型进行可量化和可重复的表型评估

Lemberg Katharina, Mertens Nils D, Yousef Kirollos, Schneider Ronen, Merz Lea M, Mansour Bshara, Salmanullah Daanya, Kolvenbach Caroline M, Saida Ken, Yu Seyoung, Hölzel Selina, Steinsapir Andrew, Goncalves Kevin A, Nicolas Frank Camille, Franken Gijs A C, Shril Shirlee, Buerger Florian, Hildebrandt Friedhelm

Quantitative phenotyping of Nphs1 knockout mice as a prerequisite for gene replacement studies.

对 Nphs1 基因敲除小鼠进行定量表型分析是基因替代研究的先决条件

Buerger Florian, Merz Lea M, Saida Ken, Yu Seyoung, Salmanullah Daanya, Lemberg Katharina, Mertens Nils D, Mansour Bshara, Kolvenbach Caroline M, Yousef Kirollos, Hölzel Selina, Braun Alina, Franken Gijs A C, Goncalves Kevin A, Steinsapir Andrew, Endlich Nicole, Schneider Ronen, Shril Shirlee, Hildebrandt Friedhelm

A homozygous truncating ETV4 variant in a Nigerian family with congenital anomalies of the kidney and urinary tract

尼日利亚一个家族中发现纯合截断型ETV4变异体,该家族患有先天性肾脏和泌尿道畸形

Kolvenbach, Caroline M; Zheng, Bixia; Merz, Lea M; Mertens, Nils D; Mansour, Bshara; Wang, Chunyan; Seltzsam, Steve; Schneider, Sophia; Schierbaum, Luca; Pantel, Dalia; Chen, Jing; van der Ven, Amelie T; Bello, Jibril O; Shril, Shirlee; Hildebrandt, Friedhelm