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Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease

Chinese medical journal, 2017-05, Vol.130 (9), p.1049-1054

2017

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Plasma neurofilament light chain concentration in the inherited peripheral neuropathies

Neurology, 2018-02, Vol.90 (6), p.e518

2018

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CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis

Journal of neurology, neurosurgery and psychiatry, 2015-08, Vol.86 (8), p.873-878

2015

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Generation of Connexin-Expressing Stable Cell Pools

Methods in molecular biology (Clifton, N.J.), 2024, Vol.2801, p.147

2024

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Genetic analysis and natural history of Charcot-Marie-Tooth disease CMTX1 due to GJB1 variants

Brain (London, England : 1878), 2023-10, Vol.146 (10), p.4336-4349

2023

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Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in Japan

Journal of neurology, neurosurgery and psychiatry, 2019-02, Vol.90 (2), p.195-202

2019

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Binding of α-synuclein oligomers to Cx32 facilitates protein uptake and transfer in neurons and oligodendrocytes

Acta neuropathologica, 2019-07, Vol.138 (1), p.23-47

2019

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Genetic heterogeneity of motor neuropathies

Neurology, 2017-03, Vol.88 (13), p.1226-1234

2017

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Knock-in mouse models for CMTX1 show a loss of function phenotype in the peripheral nervous system

Experimental neurology, 2023-02, Vol.360, p.114277-114277, Article 114277

2023

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Pattern of cell‐to‐cell transfer of microRNA by gap junction and its effect on the proliferation of glioma cells

Cancer science, 2019-06, Vol.110 (6), p.1947-1958

2019

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Cysteine residues in the C-terminal tail of connexin32 regulate its trafficking

Cellular signalling, 2021-09, Vol.85, p.110063-110063, Article 110063

2021

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Rett syndrome microglia damage dendrites and synapses by the elevated release of glutamate

The Journal of neuroscience, 2010-04, Vol.30 (15), p.5346-5356

2010

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Probenecid, a gout remedy, inhibits pannexin 1 channels

American Journal of Physiology: Cell Physiology, 2008-09, Vol.295 (3), p.C761-C767

2008

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Cross-sectional analysis of a large cohort with X-linked Charcot-Marie-Tooth disease (CMTX1)

Neurology, 2017-08, Vol.89 (9), p.927-935

2017

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Connexin32 Promotes the Activation of Foxo3a to Ameliorate Diabetic Nephropathy via Inhibiting the Polyubiquitination and Degradation of Sirt1

Antioxidants & redox signaling, 2023-08, Vol.39 (4-6), p.241-261

2023

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Intrathecal gene therapy in mouse models expressing CMT1X mutations

Human molecular genetics, 2018-04, Vol.27 (8), p.1460-1473

2018

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Gene replacement therapy after neuropathy onset provides therapeutic benefit in a model of CMT1X

Human molecular genetics, 2019-11, Vol.28 (21), p.3528-3542

2019

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Charcot-Marie-Tooth disease: genetic and clinical spectrum in a Spanish clinical series

Neurology, 2013-10, Vol.81 (18), p.1617-1625

2013

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Gene therapy approaches targeting Schwann cells for demyelinating neuropathies

Brain research, 2020-02, Vol.1728, p.146572-146572, Article 146572

2020

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Connexin 32 induces pro-tumorigenic features in MCF10A normal breast cells and MDA-MB-231 metastatic breast cancer cells

Biochimica et biophysica acta. Molecular cell research, 2020-12, Vol.1867 (12), p.118851-118851, Article 118851

2020

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Gap junctions in inherited human disorders of the central nervous system

Biochimica et biophysica acta, 2012-08, Vol.1818 (8), p.2030-2047

2012

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Targeting the colony stimulating factor 1 receptor alleviates two forms of Charcot-Marie-Tooth disease in mice

Brain (London, England : 1878), 2015-11, Vol.138 (Pt 11), p.3193-3205

2015

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Trop2: From development to disease

Developmental dynamics, 2015-02, Vol.244 (2), p.99-109

2015

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Investigating oligodendrocyte connexins: Heteromeric interactions between Cx32 and mutant or wild‐type forms of Cx47 do not contribute to or modulate gap junction function

Glia, 2021-08, Vol.69 (8), p.1882-1896

2021

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Crosstalk Between Connexin32 and Mitochondrial Apoptotic Signaling Pathway Plays a Pivotal Role in Renal Ischemia Reperfusion-Induced Acute Kidney Injury

Antioxidants & redox signaling, 2019-04, Vol.30 (12), p.1521-1538

2019

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Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease

Plasma neurofilament light chain concentration in the inherited peripheral neuropathies

CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis

Generation of Connexin-Expressing Stable Cell Pools

Genetic analysis and natural history of Charcot-Marie-Tooth disease CMTX1 due to GJB1 variants

Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in Japan

Binding of α-synuclein oligomers to Cx32 facilitates protein uptake and transfer in neurons and oligodendrocytes

Genetic heterogeneity of motor neuropathies

Knock-in mouse models for CMTX1 show a loss of function phenotype in the peripheral nervous system

Pattern of cell‐to‐cell transfer of microRNA by gap junction and its effect on the proliferation of glioma cells

Cysteine residues in the C-terminal tail of connexin32 regulate its trafficking

Rett syndrome microglia damage dendrites and synapses by the elevated release of glutamate

Probenecid, a gout remedy, inhibits pannexin 1 channels

Cross-sectional analysis of a large cohort with X-linked Charcot-Marie-Tooth disease (CMTX1)

Connexin32 Promotes the Activation of Foxo3a to Ameliorate Diabetic Nephropathy via Inhibiting the Polyubiquitination and Degradation of Sirt1

Intrathecal gene therapy in mouse models expressing CMT1X mutations

Gene replacement therapy after neuropathy onset provides therapeutic benefit in a model of CMT1X

Charcot-Marie-Tooth disease: genetic and clinical spectrum in a Spanish clinical series

Gene therapy approaches targeting Schwann cells for demyelinating neuropathies

Connexin 32 induces pro-tumorigenic features in MCF10A normal breast cells and MDA-MB-231 metastatic breast cancer cells

Gap junctions in inherited human disorders of the central nervous system

Targeting the colony stimulating factor 1 receptor alleviates two forms of Charcot-Marie-Tooth disease in mice

Trop2: From development to disease

Investigating oligodendrocyte connexins: Heteromeric interactions between Cx32 and mutant or wild‐type forms of Cx47 do not contribute to or modulate gap junction function

Crosstalk Between Connexin32 and Mitochondrial Apoptotic Signaling Pathway Plays a Pivotal Role in Renal Ischemia Reperfusion-Induced Acute Kidney Injury

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