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D

Daohua Jiang

Chinese Academy of Sciences

H指数:20

被引数:1,870

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Mechanisms of vesicular monoamine transporter 2 modulation by amphetamines and lobeline

胺类囊泡单胺转运蛋白2经苯丙胺和洛贝林调控的机制

IF6.9

2026-10-260

OA

Structural basis of glucosinolate recognition and transport by plant GTR1

植物GTR1对葡萄糖硫苷的识别和转运的结构基础

IF12.5

2026-04-010

OA

Structure and mechanism of the human bile acid transporter OSTα–OSTβ

人胆汁酸转运体ostα-ostβ 的结构和机制

IF48.5

2026-01-280

PRE

Structural mechanisms for inhibition and activation of human small-conductance Ca2+-activated potassium channel SK2

人类小电导钙激活钾通道SK2的抑制与激活的结构机制

Nature Communications

IF15.7

2026-01-150

OAAI

Dual-Proximity Labeling Strategy Identifies TrxR1 as a Cuproprotein that Regulates Apoptosis via Caspase-3 S-Nitrosylation

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

IF16.9

2026-01-010

PRE

Structural basis for transport and inhibition of the human glucose-6-phosphate transporter G6PT

人类葡萄糖-6-磷酸转运蛋白G6PT的转运与抑制的结构基础

Nature Communications

IF15.7

2025-10-240

OAAI

Structure and transport mechanism of the human prostaglandin transporter SLCO2A1

人前列腺素转运蛋白SLCO2A1的结构与转运机制

Nature Communications

IF15.7

2025-08-300

OAAI

Structural basis of auxin recognition and transport by the plant influx carrier AUX1

植物内向转运载体AUX1介导生长素识别与运输的结构基础

Molecular Plant

IF24.1

2025-06-260

OAAI

Structural insights into substrate transport and drug inhibition of the human vesicular monoamine transporter 2 (VMAT2)

对人类囊泡单胺转运蛋白2 (VMAT2) 的底物转运和药物抑制的结构见解

IF4.2

2025-01-300

OA

Structural snapshots of human VMAT2 reveal insights into substrate recognition and proton coupling mechanism

IF25.9

2024-05-220

PRE

Structural mechanism of voltage-gated sodium channel slow inactivation

NATURE COMMUNICATIONS

IF15.7

2024-05-010

OAAI

Structural insights into double-stranded RNA recognition and transport by SID-1

NATURE STRUCTURAL & MOLECULAR BIOLOGY

IF10.1

2024-04-251

PRE

Transport and inhibition mechanisms of human VMAT2

IF48.5

2023-12-110

PRE

Structural basis of human Slo2.2 channel gating and modulation

IF6.9

2023-08-018

OA

Pain-causing stinging nettle toxins target TMEM233 to modulate NaV1.7 function

NATURE COMMUNICATIONS

IF15.7

2023-04-2810

OAAI

Jami, Sina; Deuis, Jennifer R.; Klasfauseweh, Tabea; Cheng, Xiaoyang; Kurdyukov, Sergey; Chung, Felicity; Okorokov, Andrei L.; Li, Shengnan; Zhang, Jiangtao; Ben Cristofori-Armstrong; Israel, Mathilde R.; Ju, Robert J.; Robinson, Samuel D.; Zhao, Peng; Ragnarsson, Lotten; Andersson, Asa; Tran, Poanna; Schendel, Vanessa; McMahon, Kirsten L.; Tran, Hue N. T.; Chin, Yanni K. -Y.; Zhu, Yifei; Liu, Junyu; Crawford, Theo; Purushothamvasan, Saipriyaa; Habib, Abdella M.; Andersson, David A.; Rash, Lachlan D.; Wood, John N.; Zhao, Jing; Stehbens, Samantha J.; Mobli, Mehdi; Leffler, Andreas; Jiang, Daohua; Cox, James J.; Waxman, Stephen G.; Dib-Hajj, Sulayman D.; Gregory Neely, G.; Durek, Thomas; Vetter, Irina

Structure of human NaV1.6 channel reveals Na+ selectivity and pore blockade by 4,9-anhydro-tetrodotoxin

NATURE COMMUNICATIONS

IF15.7

2023-02-2316

OAAI

Structural basis for NaV1.7 inhibition by pore blockers

NATURE STRUCTURAL & MOLECULAR BIOLOGY

IF10.1

2022-11-2419

PRE

Structural basis of TRPV3 inhibition by an antagonist

NATURE CHEMICAL BIOLOGY

IF13.7

2022-10-2716

PRE

N-type fast inactivation of a eukaryotic voltage-gated sodium channel

NATURE COMMUNICATIONS

IF15.7

2022-05-1710

OAAI

Structural basis for modulation of human NaV1.3 by clinical drug and selective antagonist

NATURE COMMUNICATIONS

IF15.7

2022-03-1142

OAAI