Hongbo Xu

发表

Novel compound heterozygous mutations in the CHST6 gene cause macular corneal dystrophy in a Han Chinese family

H. Deng, Renhong Tang, Yanna Cao, 2021, Annals of translational medicine.

Identification of a Heterozygous Mutation in the TGFBI Gene in a Hui-Chinese Family with Corneal Dystrophy

H. Deng, Qin Xiang, Yanna Cao, 2019, Journal of ophthalmology.

The HIV Protease Inhibitor Saquinavir Inhibits HMGBl-Driven Inflammation by Targeting the Interaction of Cathepsin V with TLR4/MyD88

K. Tracey, Huan Yang, T. Billiar, 2015, Molecular medicine.

Immune‐Responsive Gene 1/Itaconate Activates Nuclear Factor Erythroid 2–Related Factor 2 in Hepatocytes to Protect Against Liver Ischemia–Reperfusion Injury

T. Billiar, M. Scott, Chenxuan Yang, 2020, Hepatology.

Identification of a Novel Mutation in the COL2A1 Gene in a Chinese Family with Spondyloepiphyseal Dysplasia Congenita

H. Deng, Yan Yang, Song Wu, 2015, PloS one.

Identification of a Missense Mutation in the α-galactosidase A Gene in a Chinese Family with Fabry Disease

H. Zhang, Jun Liu, H. Deng, 2017, Current genomics.

Digenic Variants in the TTN and TRAPPC11 Genes Co-segregating With a Limb-Girdle Muscular Dystrophy in a Han Chinese Family

Qian Chen, Hongbo Xu, H. Deng, 2021, Frontiers in Neuroscience.

Novel and Recurring Disease-Causing NF1 Variants in Two Chinese Families with Neurofibromatosis Type 1

Heng Xiao, Hongbo Xu, H. Deng, 2018, Journal of Molecular Neuroscience.

A novel splice‐site mutation in the ATP2C1 gene of a Chinese family with Hailey‐Hailey disease

Heng Xiao, Xiang Chen, H. Deng, 2018, Journal of cellular biochemistry.

Overexpression of long noncoding RNA LINC00882 is associated with poor prognosis in hepatocellular carcinoma

Feizhou Huang, Tao Wan, Lei Zhu, 2018, OncoTargets and therapy.

Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma

Heng Xiao, Hongwei Lu, H. Deng, 2018, Cellular Physiology and Biochemistry.

A novel FN1 variant associated with familial hematuria: TBMN?

H. Deng, W. Xiong, Yuzhou Huang, 2016, Clinical biochemistry.

Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly

Jianguo Zhang, H. Deng, H. Deng, 2016, PloS one.

Identification of a Novel GJA3 Mutation in Congenital Nuclear Cataract

Jianguo Zhang, H. Deng, W. Xiong, 2015, Optometry and vision science : official publication of the American Academy of Optometry.

Immune‐Responsive Gene 1/Itaconate Activates Nuclear Factor Erythroid 2–Related Factor 2 in Hepatocytes to Protect Against Liver Ischemia–Reperfusion Injury

T. Billiar, M. Scott, Chenxuan Yang, 2020, Hepatology (Baltimore, Md.).

Cutting Edge: Probiotics and Fecal Microbiota Transplantation in Immunomodulation

Mingyi Zhao, Quan Zhuang, Hongbo Xu, 2019, Journal of immunology research.

Identification of a novel EVC variant in a Han‐Chinese family with Ellis‐van Creveld syndrome

H. Deng, Yi Guo, Zhijian Yang, 2019, Molecular genetics & genomic medicine.

Identifying a BRCA2 c.5722_5723del mutation in a Han-Chinese family with breast cancer

Xiaorong Li, H. Deng, Shaihong Zhu, 2019, Bioscience reports.

Novel and Recurring NOTCH3 Mutations in Two Chinese Patients with CADASIL

Hongbo Xu, H. Deng, S. Deng, 2019, Neurodegenerative Diseases.

Systematic genetic analysis of the PITX3 gene in patients with Parkinson disease

J. Jankovic, H. Deng, Zhi Song, 2011, Movement disorders : official journal of the Movement Disorder Society.

Genetic analysis of the S100B gene in Chinese patients with Parkinson disease

H. Deng, Zhi Song, W. Xiong, 2013, Neuroscience Letters.

HLA rs3129882 variant in Chinese Han patients with late-onset sporadic Parkinson disease

H. Deng, Zi-qiang Luo, Wen Zheng, 2011, Neuroscience Letters.

The identification of a transthyretin variant p.D38G in a Chinese family with early-onset leptomeningeal amyloidosis

P. Mao, Hongbo Xu, H. Deng, 2018, Journal of Neurology.

Downregulation of ROS-FIG inhibits cell proliferation, colony-formation, cell cycle progression, migration and invasion, while inducing apoptosis in intrahepatic cholangiocarcinoma cells

Wei Huang, Wanpin Nie, Feizhou Huang, 2014, International journal of molecular medicine.

Identification of novel pathogenic ABCA4 variants in a Han Chinese family with Stargardt disease

Hongbo Xu, H. Deng, Lamei Yuan, 2018, Bioscience reports.

Identification of a novel mutation in the ABCA4 gene in a Chinese family with retinitis pigmentosa using exome sequencing

Y. Li, H. Deng, Wen Zheng, 2018, Bioscience reports.

Identification of a GNE homozygous mutation in a Han‐Chinese family with GNE myopathy

H. Deng, Wen Zheng, Yan Yang, 2018, Journal of cellular and molecular medicine.

Novel MFSD8 Variants in a Chinese Family with Nonsyndromic Macular Dystrophy

H. Deng, Jianming Li, J. Xiang, 2021, Journal of ophthalmology.

Compound heterozygous POMT1 mutations in a Chinese family with autosomal recessive muscular dystrophy‐dystroglycanopathy C1

H. Deng, L. Guan, Wen Zheng, 2017, Journal of cellular and molecular medicine.

Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing

H. Deng, L. Guan, Zhi Song, 2016, PloS one.

An OTOF Frameshift Variant Associated with Auditory Neuropathy Spectrum Disorder

H. Deng, P. Hu, H. Xia, 2017, Current genomics.

cGAS-mediated autophagy protects the liver from ischemia-reperfusion injury independently of STING.

T. Billiar, M. Scott, P. Loughran, 2018, American journal of physiology. Gastrointestinal and liver physiology.

Novel CLCN7 mutation identified in a Han Chinese family with autosomal dominant osteopetrosis-2

Pengfei Rong, H. Deng, Yi Guo, 2016, Molecular pain.

Analysis of the MRPL3, DNAJC13 and OFCC1 variants in Chinese Han patients with TS-CTD

L. Su, H. Deng, Zi-qiang Luo, 2012, Neuroscience Letters.

Mutation screening of the HDC gene in Chinese Han patients with Tourette syndrome

L. Su, H. Deng, Zhi Song, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Examination of the MASH1 gene in patients with Parkinson's disease.

J. Jankovic, W. Le, H. Deng, 2010, Biochemical and biophysical research communications.

Genetic Analysis of the Leucine-Rich Repeat and lg Domain Containing Nogo Receptor-Interacting Protein 1 Gene in Essential Tremor

Yongxiang Zhao, H. Deng, Wen Zheng, 2013, Journal of Molecular Neuroscience.

No evidence of association between the LINGO4 gene and essential tremor in Chinese Han patients.

H. Deng, Wen Zheng, Zhi Song, 2012, Parkinsonism & related disorders.

Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss

Guangxiang He, H. Deng, P. Hu, 2015, PloS one.

Analysis of the BTBD9 and HTR2C variants in Chinese Han patients with Tourette syndrome

L. Su, Jinsong Tang, Zuocheng Yang, 2012, Psychiatric genetics.

Gene expression changes in peripheral blood from chinese han patients with tourette syndrome

L. Su, W. Le, H. Deng, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Heterogeneous phenotype in a family with the FERM domain-containing 7 gene R335X mutation.

K. Gao, H. Deng, Wen Zheng, 2014, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

A Disease-Causing FRMD7 Variant in a Chinese Family with Infantile Nystagmus

H. Deng, Zhi Song, S. Deng, 2019, Journal of Molecular Neuroscience.