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

Regulation of the formin INF2 by actin monomers and calcium/calmodulin.

肌动蛋白单体和钙/钙调蛋白对formin INF2的调节。

Lee Miriam, Jalmukhambetova Aiman, Burgin T Emme, Higgs Henry N

INF2-Related Charcot-Marie-Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights

日本人群中INF2相关夏科-马里-图斯病:遗传学和临床见解

Yano, Chikashi; Ando, Masahiro; Higuchi, Yujiro; Yuan, Jun-Hui; Yoshimura, Akiko; Hobara, Takahiro; Nagatomo, Risa; Kojima, Fumikazu; Hiramatsu, Yu; Nozuma, Satoshi; Nakamura, Tomonori; Sakiyama, Yusuke; Matsuoka, Chika; Yamashita, Toru; Kimura, Takashi; Miyazaki, Ayako; Kinjo, Chinatsu; Yokochi, Kenji; Yamanaka, Nanami; Matsuda, Nozomu; Suichi, Tomoki; Hanaoka, Yoshiyuki; Kojima, Haruka; Todo, Kenichi; Ishiura, Hiroyuki; Mitsui, Jun; Tsuji, Shoji; Takashima, Hiroshi

Structural and functional dissection of the WH2/DAD motif of INF2, a formin linked to human inherited degenerative disorders

对 INF2(一种与人类遗传性退行性疾病相关的formin蛋白)的 WH2/DAD 基序进行结构和功能解析

Labat-de-Hoz, Leticia; Fernández-Martín, Laura; Morales, Paula; Correas, Isabel; Jiménez, María Ángeles; Alonso, Miguel Angel

Glucose Deprivation-Induced Disulfidptosis via the SLC7A11-INF2 Axis: Pan-Cancer Prognostic Exploration and Therapeutic Validation.

葡萄糖剥夺诱导的二硫键凋亡通过 SLC7A11-INF2 轴:泛癌预后探索和治疗验证。

Nerve Enlargement in Patients with INF2 Variants Causing Peripheral Neuropathy and Focal Segmental Glomerulosclerosis

携带 INF2 变异基因导致周围神经病变和局灶节段性肾小球硬化症的患者出现神经增生

Huong, Quynh Tran Thuy; Truc, Linh Tran Nguyen; Ueda, Hiroko; Fukui, Kenji; Higasa, Koichiro; Sato, Yoshinori; Takeda, Shinichi; Hattori, Motoshi; Tsukaguchi, Hiroyasu

Delayed postoperative hemorrhage (DEPOH) in an Irish Wolfhound with the SERPINF2 c.605 T/T genotype: case description and variant prevalence across dog breeds

爱尔兰猎狼犬SERPINF2 c.605 T/T基因型延迟性术后出血(DEPOH):病例描述及该变异在不同犬种中的流行情况

Court, Michael H; Hardy, Melissa; Forbes, Keith R; Yang, Hong; Jimenez, Tania Perez

Autosomal dominant focal segmental glomerulosclerosis by INF2 p.Arg218Trp and p.Ser186Pro mutations: three case reports and literature review

由 INF2 p.Arg218Trp 和 p.Ser186Pro 突变引起的常染色体显性局灶节段性肾小球硬化症:三例病例报告及文献综述

Guo, Shunian; Shang, Minghua; Su, Chao; Zhuge, Yifeng; Wei, Wenqian; Rong, Shu; Gu, Lijie

Regulation of the formin INF2 by actin monomers and calcium-calmodulin

肌动蛋白单体和钙调蛋白对formin INF2的调控

Lee, Miriam; Jalmukhambetova, Aiman; Burgin, T Emme; Higgs, Henry N

INF2 mutations cause kidney disease through a gain-of-function mechanism

INF2 突变通过获得功能机制导致肾脏疾病

Balajikarthick Subramanian, Sarah Williams, Sophie Karp, Marie-Flore Hennino, Sonako Jacas, Miriam Lee, Cristian V Riella, Seth L Alper, Henry N Higgs, Martin R Pollak

Regulation of formin INF2 and its alteration in INF2-linked inherited disorders

调控蛋白INF2及其在INF2相关遗传疾病中的改变

Labat-de-Hoz, Leticia; Jiménez, M Ángeles; Correas, Isabel; Alonso, Miguel A