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

Blended Phenotypes of Sexual Development Disorder and Coenzyme Q10 Deficiency, Together with a Sibling with Homozygous Variants in the AHI1 Gene

性发育障碍和辅酶Q10缺乏症的混合表型,以及其兄弟姐妹携带AHI1基因纯合变异

Atasay, Rumeysa; Yilmaz, Leyla Nur; Gulec, Ayten; Canpolat, Mehmet; Per, Huseyin; Kardas, Fatih; Ozsait Selcuk, Bilge; Karaman, Birsen; Kiraz, Aslihan; Dundar, Munis

Common Risk Variants in AHI1 Are Associated With Childhood Steroid Sensitive Nephrotic Syndrome

AHI1基因的常见风险变异与儿童类固醇敏感性肾病综合征相关

Downie, Mallory L; Gupta, Sanjana; Voinescu, Catalin; Levine, Adam P; Sadeghi-Alavijeh, Omid; Dufek-Kamperis, Stephanie; Cao, Jingjing; Christian, Martin; Kari, Jameela A; Thalgahagoda, Shenal; Ranawaka, Randula; Abeyagunawardena, Asiri; Gbadegesin, Rasheed; Parekh, Rulan; Kleta, Robert; Bockenhauer, Detlef; Stanescu, Horia C; Gale, Daniel P

Cycloheximide (CHX) Chase Assay to Examine Protein Half-life

环己酰亚胺 (CHX) 追踪试验检测蛋白质半衰期

Ying Miao, Qian Du, Hong-Guang Zhang, Yukang Yuan, Yibo Zuo, Hui Zheng

Depression compromises antiviral innate immunity via the AVP-AHI1-Tyk2 axis

抑郁症通过 AVP-AHI1-Tyk2 轴损害抗病毒先天免疫力。

Hong-Guang Zhang # ,Bin Wang # ,Yong Yang ,Xuan Liu ,Junjie Wang ,Ning Xin ,Shifeng Li ,Ying Miao ,Qiuyu Wu ,Tingting Guo ,Yukang Yuan ,Yibo Zuo ,Xiangjie Chen ,Tengfei Ren ,Chunsheng Dong ,Jun Wang ,Hang Ruan ,Miao Sun ,Xingshun Xu ,Hui Zheng

AHI1: linking depression and impaired antiviral immune response

AHI1:抑郁症与抗病毒免疫反应受损之间的联系

Yang, Weili; Li, Shihua; Li, Xiao-Jiang

Retinitis pigmentosa and molar tooth sign caused by novel AHI1 compound heterozygote pathogenic variants

由新型AHI1复合杂合致病变异引起的视网膜色素变性和臼齿征

Chunyan Chen # ,Jiong Gao # ,Qing Lv # ,Chen Xu ,Yu Xia ,Ailian Du

AHI1 gene mutation in a consanguineous Iranian family affected by Joubert syndrome: A case report

伊朗近亲结婚家族中AHI1基因突变导致Joubert综合征:病例报告

Neissi, Mostafa; Mabudi, Hadideh; Mohammadi-Asl, Javad

MS AHI1 genetic risk promotes IFNγ(+) CD4(+) T cells

MS AHI1 基因风险促进 IFNγ(+) CD4(+) T 细胞

Kaskow, Belinda J; Buttrick, Thomas S; Klein, Hans-Ulrich; White, Charles; Bourgeois, Justin R; Ferland, Russell J; Patsopoulos, Nikolaos; Bradshaw, Elizabeth M; De Jager, Philip L; Elyaman, Wassim

The multiple sclerosis risk allele within the AHI1 gene is associated with relapses in children and adults

AHI1基因内的多发性硬化症风险等位基因与儿童和成人的复发有关

Graves, Jennifer S; Barcellos, Lisa F; Simpson, Steve; Belman, Anita; Lin, Rui; Taylor, Bruce V; Ponsonby, Anne-Louise; Dwyer, Terence; Krupp, Lauren; Waubant, Emmanuelle; van der Mei, Ingrid A F

Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency

PVT1、ATG13-AMBRA1、AHI1 和 CLEC16A 的常见变异与选择性 IgA 缺乏症相关。

Bronson, Paola G; Chang, Diana; Bhangale, Tushar; Seldin, Michael F; Ortmann, Ward; Ferreira, Ricardo C; Urcelay, Elena; Pereira, Luis Fernández; Martin, Javier; Plebani, Alessandro; Lougaris, Vassilios; Friman, Vanda; Freiberger, Tomáš; Litzman, Jiri; Thon, Vojtech; Pan-Hammarström, Qiang; Hammarström, Lennart; Graham, Robert R; Behrens, Timothy W