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

Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome.

AEBP1 的双等位基因改变导致胶原蛋白组装和结缔组织结构缺陷,从而导致埃勒斯-当洛斯综合征的变异型

Blackburn Patrick R, Xu Zhi, Tumelty Kathleen E, Zhao Rose W, Monis William J, Harris Kimberly G, Gass Jennifer M, Cousin Margot A, Boczek Nicole J, Mitkov Mario V, Cappel Mark A, Francomano Clair A, Parisi Joseph E, Klee Eric W, Faqeih Eissa, Alkuraya Fowzan S, Layne Matthew D, McDonnell Nazli B, Atwal Paldeep S

Neurodevelopmental disease mechanisms, primary cilia, and endosomes converge on the BLOC-1 and BORC complexes

神经发育疾病机制、初级纤毛和内体都与BLOC-1和BORC复合物密切相关。

Hartwig, Cortnie; Monis, William J; Chen, Xun; Dickman, Dion K; Pazour, Gregory J; Faundez, Victor

Loss of Arf4 causes severe degeneration of the exocrine pancreas but not cystic kidney disease or retinal degeneration

Arf4基因缺失会导致外分泌胰腺严重退化,但不会引起囊性肾病或视网膜退化。

Pearring, Jillian N; San Agustin, Jovenal T; Lobanova, Ekaterina S; Gabriel, Christopher J; Lieu, Eric C; Monis, William J; Stuck, Michael W; Strittmatter, Lara; Jaber, Samer M; Arshavsky, Vadim Y; Pazour, Gregory J