文献库，生知库 | 链接生命科学的每一步

The linker histone chaperone Prothymosin Î± (PTMA) is essential for efficient DNA damage repair and the recruitment of PARP1.

连接组蛋白伴侣蛋白Prothymosin Î± (PTMA) 对于有效的DNA损伤修复和PARP1的募集至关重要

期刊:Epigenetics & Chromatin

影响因子:3.5

doi:10.1186/s13072-025-00599-1

McKnight Ciara A, Graichen Mary E, George Eric M, Brown David T

毒理研究

发表日期：2025

文献求助收藏

Fully synthetic matrices for in vitro culture of primary human intestinal enteroids and endometrial organoids

用于体外培养原代人类肠道类器官和子宫内膜类器官的全合成基质

期刊:Biomaterials

影响因子:12.8

doi:10.1016/j.biomaterials.2020.120125

Victor Hernandez-Gordillo, Timothy Kassis, Arinola Lampejo, GiHun Choi, Mario E Gamboa, Juan S Gnecco, Alexander Brown, David T Breault, Rebecca Carrier, Linda G Griffith

PARP1-dependent eviction of the linker histone H1 mediates immediate early gene expression during neuronal activation

PARP1依赖的连接组蛋白H1的移除介导神经元激活过程中的早期基因表达

期刊:Journal of Cell Biology

影响因子:6.4

doi:10.1083/jcb.201703141

Azad, Gajendra Kumar; Ito, Kenji; Sailaja, Badi Sri; Biran, Alva; Nissim-Rafinia, Malka; Yamada, Yasuhiro; Brown, David T; Takizawa, Takumi; Meshorer, Eran

Differential lipid binding of vinculin isoforms promotes quasi-equivalent dimerization

黏着斑蛋白亚型的差异性脂质结合促进准等价二聚化

期刊:Proceedings of the National Academy of Sciences of the United States of America

影响因子:9.1

doi:10.1073/pnas.1600702113

Chinthalapudi, Krishna; Rangarajan, Erumbi S; Brown, David T; Izard, Tina

发表日期：2016

文献求助收藏

Mechanisms and Functions of Vinculin Interactions with Phospholipids at Cell Adhesion Sites

黏着斑蛋白与细胞黏附位点磷脂相互作用的机制和功能

期刊:Journal of Biological Chemistry

影响因子:3.9

doi:10.1074/jbc.R115.686493

Izard, Tina; Brown, David T

Photobleaching studies reveal that a single amino acid polymorphism is responsible for the differential binding affinities of linker histone subtypes H1.1 and H1.5

光漂白研究表明，单个氨基酸多态性是连接组蛋白亚型 H1.1 和 H1.5 结合亲和力差异的原因。

期刊:Biology Open

影响因子:1.7

doi:10.1242/bio.016733

Flanagan, Thomas W; Files, Jacob K; Casano, Kelsey Rose; George, Eric M; Brown, David T

发表日期：2016

文献求助收藏

Vinculin-cell membrane interactions

黏着斑蛋白-细胞膜相互作用

期刊:Oncotarget

影响因子:

doi:10.18632/oncotarget.5868

Brown, David T; Izard, Tina

细胞生物学

发表日期：2015

文献求助收藏

Dissecting the binding mechanism of the linker histone in live cells: an integrated FRAP analysis

解析活细胞中连接组蛋白的结合机制：一项整合的FRAP分析

期刊:EMBO Journal

影响因子:8.3

doi:10.1038/emboj.2010.24

Stasevich, Timothy J; Mueller, Florian; Brown, David T; McNally, James G

细胞生物学

发表日期：2010

文献求助收藏

Nucleosome interaction surface of linker histone H1c is distinct from that of H1(0)

连接组蛋白 H1c 的核小体相互作用表面与 H1(0) 的核小体相互作用表面不同。

期刊:Journal of Biological Chemistry

影响因子:3.9

doi:10.1074/jbc.M110.108639

George, Eric M; Izard, Tina; Anderson, Stephen D; Brown, David T

发表日期：2010

文献求助收藏

Coilin and SUMOylation influence PARP1 dynamics and the DNA damage response

Coilin 和 SUMO 化影响 PARP1 的动态变化和 DNA 损伤反应

The linker histone chaperone Prothymosin Î± (PTMA) is essential for efficient DNA damage repair and the recruitment of PARP1.

连接组蛋白伴侣蛋白Prothymosin Î± (PTMA) 对于有效的DNA损伤修复和PARP1的募集至关重要

Fully synthetic matrices for in vitro culture of primary human intestinal enteroids and endometrial organoids

用于体外培养原代人类肠道类器官和子宫内膜类器官的全合成基质

PARP1-dependent eviction of the linker histone H1 mediates immediate early gene expression during neuronal activation

PARP1依赖的连接组蛋白H1的移除介导神经元激活过程中的早期基因表达

Differential lipid binding of vinculin isoforms promotes quasi-equivalent dimerization

黏着斑蛋白亚型的差异性脂质结合促进准等价二聚化

Mechanisms and Functions of Vinculin Interactions with Phospholipids at Cell Adhesion Sites

黏着斑蛋白与细胞黏附位点磷脂相互作用的机制和功能

Photobleaching studies reveal that a single amino acid polymorphism is responsible for the differential binding affinities of linker histone subtypes H1.1 and H1.5

光漂白研究表明，单个氨基酸多态性是连接组蛋白亚型 H1.1 和 H1.5 结合亲和力差异的原因。

Vinculin-cell membrane interactions

黏着斑蛋白-细胞膜相互作用

Dissecting the binding mechanism of the linker histone in live cells: an integrated FRAP analysis

解析活细胞中连接组蛋白的结合机制：一项整合的FRAP分析

Nucleosome interaction surface of linker histone H1c is distinct from that of H1(0)

连接组蛋白 H1c 的核小体相互作用表面与 H1(0) 的核小体相互作用表面不同。