Xiaoting Lou - Zhejiang Provincial People's Hospital

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论文共 17 篇作者统计合作学者相似作者

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Expanding the Phenotypic and Genetic Spectrum of GTPBP3 Deficiency: Findings from Nine Chinese Pedigrees

Yaojun Xie, Keyi Li,Yang Li, Xiaofei Zeng,Zhehui Chen,Xue Ma,Luyi Zhang,Yuwei Zhou,Liqin Jin, Yanlin Yang,Xiaoting Lou

crossref（2024）

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Integrative multi-omics profiling reveals the molecular subtypes and circulating biomarkers for pediatric mitochondrial disease

Jianxin Lyu,Xiaoting Lou,Zhehui Chen,Qiongya Zhao,Yuwei Zhou, Xiaofei Zeng, Mei Xue, Pei Luo, Chunxia Zhang,Luyi Zhang,Yaojun Xie,Ya Wang,Qiyu Dong, Xin Yin,Tiannan Guo,Hezhi Fang,Yanling Yang

Research Square (Research Square) (2023)

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De Novo Frameshift Variant in MT-ND1 Causes a Mitochondrial Complex I Deficiency Associated with MELAS Syndrome

Xiaoting Lou,Yuwei Zhou,Zhimei Liu,Yaojun Xie,Luyi Zhang,Suzhou Zhao,Shuai Gong,Xiuwei Zhuo,Junling Wang,Lifang Dai,Xiaotun Ren,Xiao Tong, Liangliang Jiang,Hezhi Fang, Fang,Jianxin Lyu

Gene (2023)

引用1浏览0WOS引用

Novel biallelic mutations in TMEM126B cause splicing defects and lead to Leigh-like syndrome with severe complex I deficiency

Xiyue Zhou,Xiaoting Lou,Yuwei Zhou,Yaojun Xie,Xinyu Han,Qiyu Dong,Xiaojie Ying,Mahlatsi Refiloe Laurentinah,Luyi Zhang,Zhehui Chen,Dongxiao Li,Hezhi Fang,Jianxin Lyu,Yanling Yang,Ya Wang

JOURNAL OF HUMAN GENETICS（2022）

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Novel biallelic mutations in TMEM126B cause splicing defects and lead to Leigh syndrome with severe complex I deficiency

Ya Wang,Xiyue Zhou,Xiaoting Lou,Yuwei Zhou,Yaojun Xie,Qiyu Dong,Xiaojie Ying,Mahlatsi Refiloe Laurentinah,Luyi Zhang,Zhehui Chen,Dongxiao Li,Hezhi Fang,Jianxin Lu,Yang yanling

Authorea (Authorea) (2022)

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Biallelic Mutations in ACACA Cause a Disruption in Lipid Homeostasis That is Associated with Global Developmental Delay, Microcephaly, and Dysmorphic Facial Features

Xiaoting Lou,Xiyue Zhou, Haiyan Li,Xiangpeng Lu,Xinzhu Bao,Kaiqiang Yang,Xin Liao,Hanxiao Chen,Hezhi Fang,Yanling Yang,Jianxin Lyu,Hong Zheng

Frontiers in Cell and Developmental Biology（2021）

引用4浏览0WOS引用

Mitochondrial Genome Variant M.3250t>C As A Possible Risk Factor For Mitochondrial Cardiomyopathy

Teresa Campbell,Xiaoting Lou,Jesse Slone,Jenice Brown,Meghan Bromwell,Jie Liu,Renkui Bai,Katrina Haude,Amanda Balog,Hong Cui,Weiwei Zou,Li Yang,Ali Al-Beshri,Taosheng Huang

HUMAN MUTATION（2021）

引用5浏览0WOS引用

Association of Macrophage Inhibitory Factor -1 Polymorphisms with Antiviral Efficacy of Type 1b Chronic Hepatitis C

Songdao Ye,Yao Chen,Xiaoting Lou,Xuanmei Ye,Xunjun Yang

Molecular and Cellular Biochemistryno. 6 (2021): 2439-2447

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Nanoscopic quantification of sub-mitochondrial morphology, mitophagy and mitochondrial dynamics in living cells derived from patients with mitochondrial diseases

Weiwei Zou,Qixin Chen,Jesse Slone,Li Yang,Xiaoting Lou,Jiajie Diao,Taosheng Huang

JOURNAL OF NANOBIOTECHNOLOGY（2021）

引用8浏览0WOS引用

Prenatal Diagnosis and Preimplantation Genetic Diagnosis

Chengcheng Liu,Xiaoting Lou,Jianxin Lyu,Jian Wang,Yufei Xu

Clinical Molecular Diagnosticspp.769-800, (2021)

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