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

Cryo-EM structure of cadmium-bound human ABCB6

镉结合的人类ABCB6蛋白的冷冻电镜结构

Choi, Seung Hun; Lee, Sang Soo; Lee, Hyeon You; Kim, Subin; Kim, Ji Won; Jin, Mi Sun

Identification of two novel heterodimeric ABC transporters in melanoma: ABCB5β/B6 and ABCB5β/B9

黑色素瘤中两种新型异二聚体ABC转运蛋白的鉴定:ABCB5β/B6和ABCB5β/B9

Louise Gerard ,Laurent Duvivier ,Marie Fourrez ,Paula Salazar ,Lindsay Sprimont ,Di Xia ,Suresh V Ambudkar ,Michael M Gottesman ,Jean-Pierre Gillet

W546 stacking disruption traps the human porphyrin transporter ABCB6 in an outward-facing transient state

W546 堆叠破坏使人卟啉转运蛋白 ABCB6 处于一种向外开放的瞬态状态。

Lee, Sang Soo; Park, Jun Gyou; Jang, Eunhong; Choi, Seung Hun; Kim, Subin; Kim, Ji Won; Jin, Mi Sun

Hereditary anemia caused by multilocus inheritance of PIEZO1, SLC4A1 and ABCB6 mutations: a diagnostic and therapeutic challenge

由PIEZO1、SLC4A1和ABCB6基因突变多位点遗传引起的遗传性贫血:诊断和治疗的挑战

Rosato, Barbara Eleni; Alper, Seth L; Tomaiuolo, Giovanna; Russo, Roberta; Iolascon, Achille; Andolfo, Immacolata

ABCB6 polymorphisms are not overly represented in patients with porphyria

ABCB6基因多态性在卟啉症患者中并不常见。

Colin P Farrell,Gäel Nicolas,Robert J Desnick,Charles J Parker,Jerome Lamoril,Laurent Gouya,Zoubida Karim,Dimitri Tchernitchko,Brenden Chan,Herve Puy,John D Phillips

P1537: HEREDITARY ANEMIA CAUSED BY MULTILOCUS INHERITANCE OF PIEZO1, SLC4A1 AND ABCB6 MUTATIONS: A DIAGNOSTIC AND THERAPEUTIC CHALLENGE

P1537:由PIEZO1、SLC4A1和ABCB6基因突变多位点遗传引起的遗传性贫血:诊断和治疗的挑战

Kelly, Jessica M; Perseghin, Andrea; Dow, Alan W; Trivedi, Shreya P; Rodman, Adam; Berk, Justin; Derman, B; Rosenblatt, J; Avigan, D; Major, A; Rampurwala, M; Barnidge, D; Stefka, A; Jiang, K; Jakubowiak, A; Rosato, B E; Alper, S L; Tomaiuolo, G; Russo, R; Iolascon, A; Andolfo, I

A novel mutation in ABCB6 associated with dyschromatosis universalis hereditaria in a Saudi family

沙特阿拉伯一个家族中发现与遗传性泛发性色素异常症相关的ABCB6基因新突变

Aldokhayel, Sara; Nouf, Alballa; Khalid, Aleedan; Faisal, Alsaif; Maram, Alotaibi; Ahmed, Alhumidi; Fahad, Alsaif

Molecular insights into the human ABCB6 transporter

人类 ABCB6 转运蛋白的分子见解

Guangyuan Song #, Sensen Zhang #, Mengqi Tian #, Laixing Zhang #, Runyu Guo, Wei Zhuo, Maojun Yang

ALX1-related frontonasal dysplasia results from defective neural crest cell development and migration

ALX1相关性额鼻发育不良是由神经嵴细胞发育和迁移缺陷引起的。

Jonathan Pini # ,Janina Kueper # ,Yiyuan David Hu ,Kenta Kawasaki ,Pan Yeung ,Casey Tsimbal ,Baul Yoon ,Nikkola Carmichael ,Richard L Maas ,Justin Cotney ,Yevgenya Grinblat ,Eric C Liao

Cryo-electron microscopy structure of human ABCB6 transporter

人类 ABCB6 转运体的低温电子显微镜结构

Chunyu Wang, Can Cao, Nan Wang, Xiangxi Wang, Xianping Wang, Xuejun C Zhang