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

Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract.

人类肾脏和泌尿道先天性异常中茶衫锌指同源框 3 (TSHZ3) 基因的杂合变异

Kesdiren Esra, Martens Helge, Brand Frank, Werfel Lina, Wedekind Lukas, Trowe Mark-Oliver, Schmitz Jessica, Hennies Imke, Geffers Robert, Gucev Zoran, Seeman Tomáš, Schmidt Sonja, Tasic Velibor, Fasano Laurent, Bräsen Jan H, Kispert Andreas, Christians Anne, Haffner Dieter, Weber Ruthild G

PPARG contributes to urothelial integrity in the murine ureter by activating the expression of Shh and superficial cell-specific genes.

PPARG 通过激活 Shh 和表面细胞特异性基因的表达,促进小鼠输尿管尿路上皮的完整性

Rudat Carsten, Straube Philipp, Hegermann Jan, Trowe Mark-Oliver, Thiesler Hauke, Hildebrandt Herbert, Witt Lisa, Kispert Andreas

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

A 3D iPSC-differentiation model identifies interleukin-3 as a regulator of early human hematopoietic specification

三维诱导多能干细胞分化模型鉴定出白细胞介素-3是早期人类造血细胞分化的调节因子。

Ackermann, Mania; Haake, Kathrin; Kempf, Henning; Kaschutnig, Paul; Weiss, Anna-Carina; Nguyen, Ariane H H; Abeln, Markus; Merkert, Sylvia; Kühnel, Mark Phillip; Hartmann, Dorothee; Jonigk, Danny; Thum, Thomas; Kispert, Andreas; Milsom, Michael D; Lachmann, Nico

Rare heterozygous GDF6 variants in patients with renal anomalies.

肾脏畸形患者中罕见的杂合 GDF6 变异

Martens Helge, Hennies Imke, Getwan Maike, Christians Anne, Weiss Anna-Carina, Brand Frank, Gjerstad Ann Christin, Christians Arne, Gucev Zoran, Geffers Robert, Seeman Tomáš, Kispert Andreas, Tasic Velibor, Bjerre Anna, Lienkamp Soeren S, Haffner Dieter, Weber Ruthild G

Tbx15 Defines a Glycolytic Subpopulation and White Adipocyte Heterogeneity

Tbx15 定义了糖酵解亚群和白色脂肪细胞异质性

Lee, Kevin Y; Sharma, Rita; Gase, Grant; Ussar, Siegfried; Li, Yichao; Welch, Lonnie; Berryman, Darlene E; Kispert, Andreas; Bluher, Matthias; Kahn, C Ronald

Tbx15 controls skeletal muscle fibre-type determination and muscle metabolism.

Tbx15 控制骨骼肌纤维类型的决定和肌肉代谢

Lee Kevin Y, Singh Manvendra K, Ussar Siegfried, Wetzel Petra, Hirshman Michael F, Goodyear Laurie J, Kispert Andreas, Kahn C Ronald

Tbx2 terminates shh/fgf signaling in the developing mouse limb bud by direct repression of gremlin1

Tbx2通过直接抑制gremlin1来终止发育中小鼠肢芽中的shh/fgf信号传导。

Farin, Henner F; Lüdtke, Timo H-W; Schmidt, Martina K; Placzko, Susann; Schuster-Gossler, Karin; Petry, Marianne; Christoffels, Vincent M; Kispert, Andreas

Inhibition of Sox2-dependent activation of Shh in the ventral diencephalon by Tbx3 is required for formation of the neurohypophysis

Tbx3抑制腹侧间脑中Sox2依赖的Shh激活是神经垂体形成所必需的。

Trowe, Mark-Oliver; Zhao, Li; Weiss, Anna-Carina; Christoffels, Vincent; Epstein, Douglas J; Kispert, Andreas

Phenotypical analysis of atypical PKCs in vivo function display a compensatory system at mouse embryonic day 7.5.

对体内非典型 PKC 的表型分析显示,在小鼠胚胎第 7.5 天存在补偿系统

Seidl Sebastian, Braun Ursula, Roos Norbert, Li Shaohua, Lüdtke Timo H-W, Kispert Andreas, Leitges Michael