Kunqian Ji

Research Institute of Neuromuscular and Neurodegenerative Diseases

H指数:15

被引数:1,083

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Targeting taurine metabolism improves mitochondrial function in mt-tRNA mutation-associated mitochondrial disease

靶向牛磺酸代谢改善mt-tRNA突变相关线粒体疾病的线粒体功能

Orphanet Journal of Rare Diseases

IF3.5

2026-10-260

OAAI

The Case of a 19-Year-Old Woman Presenting With Headache and Transient Loss of Consciousness

一位19岁女性头痛并伴有短暂意识丧失的病例

Annals of Clinical and Translational Neurology

IF3.9

2026-03-190

OAAI

A Case of Cerebral Cortical Encephalitis

一例大脑皮质脑炎

Annals of Clinical and Translational Neurology

IF3.9

2026-03-150

OAAI

A novel tRNASer(AGY) 12244G > a variant impairs mitochondrial function and presents with classical MELAS phenotype

一种新型的tRNASer(AGY) 12244G > a变异损害线粒体功能，并表现出典型的MELAS表型。

Neurological Sciences

IF2.4

2026-02-160

PRE

Computational design of a high-precision mitochondrial DNA cytosine base editor

高精度线粒体DNA胞嘧啶碱基编辑器的计算设计

Nature Structural & Molecular Biology

IF10.1

2025-11-170

The Case of a 25-Year-Old Woman With Isolated Head Tremor

一位25岁女性孤立性头部震颤的病例

Annals of Clinical and Translational Neurology

IF3.9

2025-10-090

OAAI

Lactate-driven histone lactylation enhances GDF15 secretion in skeletal muscle under mtDNA mutation-induced mitochondrial stress

乳酸驱动的组蛋白乳酰化在mtDNA突变诱导的线粒体应激下增强骨骼肌中GDF15的分泌

Science Bulletin

IF21.1

2025-09-290

PRE

Genotype-Phenotype Correlation in Progressive External Ophthalmoplegia: Insights From a Retrospective Analysis

NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

IF3.4

2025-01-170

PRE

Taurine hypomodification underlies mitochondrial tRNATrp-related genetic diseases

NUCLEIC ACIDS RESEARCH

IF13.1

2024-10-090

OAAI

Queuine ameliorates impaired mitochondrial function caused by mt-tRNAAsn variants

JOURNAL OF TRANSLATIONAL MEDICINE

IF7.5

2024-08-220

OAAI

HiFi long-read amplicon sequencing for full-spectrum variants of human mtDNA (vol 25, 538, 2024)

BMC GENOMICS

IF3.7

2024-07-301

OAAI

Targeting DRP1 with Mdivi-1 to correct mitochondrial abnormalities in ADOA plus syndrome

JCI INSIGHT

IF6.1

2024-06-253

HiFi long-read amplicon sequencing for full-spectrum variants of human mtDNA

BMC GENOMICS

IF3.7

2024-05-310

OAAI

Unraveling the Diagnostic Puzzle: Minor Stroke-Like Lesions and Normal Muscle Histopathology in MELAS Syndrome

STROKE

IF8.9

2024-04-010

PRE

Novel Presentation of McLeod Syndrome With Muscle Weakness and Biopsy Findings Indicative of Mitochondrial Dysfunction

JOURNAL OF CLINICAL NEUROLOGY

IF3.1

2024-01-010

OAAI

Coupling MoSe2 with Non-Stoichiometry Ni0.85Se in Carbon Hollow Nanoflowers for Efficient Electrocatalytic Synergistic Effect on Li-O2 Batteries

碳空心纳米花中MoSe2与非化学计量Ni0.85Se的耦合对Li-O2电池的高效电催化协同作用

SMALL

IF12.1

2023-10-274

PRE

Shedding Light on Lysosomal Malondialdehyde Affecting Vitamin B12 Transport during Cerebral Ischemia/Reperfusion Injury

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

IF15.6

2023-10-077

PRE

A Missense Variant in AIFM1 Caused Mitochondrial Dysfunction and Intolerance to Riboflavin Deficiency

NEUROMOLECULAR MEDICINE

IF3.9

2023-08-210

PRE

A different pattern of clinical, muscle pathology and brain MRI findings in MELAS with mt-ND variants

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY

IF3.9

2023-05-236

OAAI

Reversible cerebral artery constriction accompanied with stroke-like episode in MELAS: A case series

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2022-10-011

PRE

Kunqian Ji

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