红细胞中Asp669Tyr Piezo1阳离子通道活性的表征：一种意外的表型。 - Suppr | 超能文献

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1

Characterisation of Asp669Tyr Piezo1 cation channel activity in red blood cells: an unexpected phenotype.红细胞中Asp669Tyr Piezo1阳离子通道活性的表征：一种意外的表型。

Br J Haematol. 2021 Jul;194(1):e51-e55. doi: 10.1111/bjh.17467. Epub 2021 May 11.

2

Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ hereditary xerocytosis red cells.红细胞离子含量和脱水调节 KCNN4 V282M/+遗传性非球形细胞增多症红细胞中最大 Gardos 通道活性。

Am J Physiol Cell Physiol. 2019 Aug 1;317(2):C287-C302. doi: 10.1152/ajpcell.00074.2019. Epub 2019 May 15.

3

Erythrocytes from hereditary xerocytosis patients heterozygous for KCNN4 V282M exhibit increased spontaneous Gardos channel-like activity inhibited by senicapoc.对于KCNN4 V282M杂合的遗传性口形红细胞增多症患者，其红细胞表现出自发性加尔多斯通道样活性增加，且该活性受到司尼可泊抑制。

Am J Hematol. 2017 Jun;92(6):E108-E110. doi: 10.1002/ajh.24716. Epub 2017 Apr 29.

4

Dehydrated stomatocytic anemia due to the heterozygous mutation R2456H in the mechanosensitive cation channel PIEZO1: a case report.机械敏感性阳离子通道PIEZO1中杂合突变R2456H导致的脱水口形红细胞贫血：一例报告

Blood Cells Mol Dis. 2014 Jan;52(1):53-4. doi: 10.1016/j.bcmd.2013.07.015. Epub 2013 Aug 23.

5

RBCs prevent rapid PIEZO1 inactivation and expose slow deactivation as a mechanism of dehydrated hereditary stomatocytosis.红细胞可防止PIEZO1快速失活，并将缓慢失活作为脱水遗传性口形红细胞增多症的一种机制表现出来。

Blood. 2020 Jul 2;136(1):140-144. doi: 10.1182/blood.2019004174.

6

Mild erythrocytosis as a presenting manifestation of associated erythrocyte volume disorders.轻度红细胞增多症作为相关红细胞体积紊乱的首发表现。

Pediatr Hematol Oncol. 2019 Aug;36(5):317-326. doi: 10.1080/08880018.2019.1637984. Epub 2019 Jul 12.

7

Congenital hemolytic anemia with high-sodium, low-potassium red cells. Studies of three generations of a family with a new variant.伴有高钠低钾红细胞的先天性溶血性贫血。一个具有新变异型的家族三代人的研究。

N Engl J Med. 1969 Apr 24;280(17):909-16. doi: 10.1056/NEJM196904242801701.

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Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels.与机械激活的 PIEZO1 离子通道功能获得性突变相关的脱水遗传性口炎性腹泻。

Nat Commun. 2013;4:1884. doi: 10.1038/ncomms2899.

9

Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in India.机械敏感型 Piezo1 离子通道蛋白（PIEZO1 基因）：对印度遗传性血红细胞增多症的更新和扩展突变分析。

Ann Hematol. 2020 Apr;99(4):715-727. doi: 10.1007/s00277-020-03955-1. Epub 2020 Feb 28.

10

A new variant of hereditary hemolytic anemia with stomatocytosis and erythrocyte cation abnormality.一种伴有口形红细胞增多症和红细胞阳离子异常的遗传性溶血性贫血新变种。

Blood. 1971 Aug;38(2):184-204.

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Dual action of Dooku1 on PIEZO1 channel in human red blood cells.杜库1对人红细胞中PIEZO1通道的双重作用。

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