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

Testis Determination Requires a Specific FGFR2 Isoform to Repress FOXL2

睾丸决定需要特定的 FGFR2 同工型来抑制 FOXL2

Stefan Bagheri-Fam, Anthony D Bird, Liang Zhao, Janelle M Ryan, Meiyun Yong, Dagmar Wilhelm, Peter Koopman, Veraragavan P Eswarakumar, Vincent R Harley

Combined KIT and FGFR2b signaling regulates epithelial progenitor expansion during organogenesis

KIT和FGFR2b信号通路联合调控器官发生过程中上皮祖细胞的扩增。

Lombaert, Isabelle M A; Abrams, Shaun R; Li, Li; Eswarakumar, Veraragavan P; Sethi, Aditya J; Witt, Robert L; Hoffman, Matthew P

Ureteric morphogenesis requires Fgfr1 and Fgfr2/Frs2α signaling in the metanephric mesenchyme

输尿管形态发生需要后肾间充质中的 Fgfr1 和 Fgfr2/Frs2α 信号传导

Sunder Sims-Lucas, Valeria Di Giovanni, Caitlin Schaefer, Brian Cusack, Veraragavan P Eswarakumar, Carlton M Bates

Independent roles of Fgfr2 and Frs2alpha in ureteric epithelium

Fgfr2 和 Frs2alpha 在输尿管上皮中的独立作用

Sunder Sims-Lucas, Brian Cusack, Veraragavan P Eswarakumar, Jue Zhang, Fen Wang, Carlton M Bates

Fgfr1 and the IIIc isoform of Fgfr2 play critical roles in the metanephric mesenchyme mediating early inductive events in kidney development

Fgfr1 和 Fgfr2 的 IIIc 亚型在后肾间充质中发挥关键作用,介导肾脏发育早期的诱导事件。

Sims-Lucas, Sunder; Cusack, Brian; Baust, Jeffrey; Eswarakumar, Veraragavan P; Masatoshi, Hagiwara; Takeuchi, Akihide; Bates, Carlton M

Deletion of Frs2alpha from the ureteric epithelium causes renal hypoplasia

输尿管上皮细胞中Frs2α基因的缺失会导致肾发育不全

Sims-Lucas, Sunder; Cullen-McEwen, Luise; Eswarakumar, Veraragavan P; Hains, David; Kish, Kayle; Becknell, Brian; Zhang, Jue; Bertram, John F; Wang, Fen; Bates, Carlton M

Lacrimo-auriculo-dento-digital syndrome is caused by reduced activity of the fibroblast growth factor 10 (FGF10)-FGF receptor 2 signaling pathway

泪耳牙指综合征是由成纤维细胞生长因子10 (FGF10)-FGF受体2信号通路活性降低引起的。

Shams, Imad; Rohmann, Edyta; Eswarakumar, Veraragavan P; Lew, Erin D; Yuzawa, Satoru; Wollnik, Bernd; Schlessinger, Joseph; Lax, Irit

A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis

Fgfr2c 的功能获得性突变揭示了该受体变体在成骨作用中的作用

Eswarakumar, Veraragavan P; Horowitz, Mark C; Locklin, Rachel; Morriss-Kay, Gillian M; Lonai, Peter