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Role of PGC-1α in Mitochondrial Quality Control in Neurodegenerative Diseases

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  1. Article

    Open Access

    Early versus late diagnosis of LAMA2 congenital muscular dystrophy: a distinct consequence

    Laminin subunit alpha 2 (LAMA2)-related muscular dystrophy (LAMA2 MD) is caused by homozygous or compound heterozygous mutations in LAMA2 (OMIM#156225), located on chromosome 6q22.

    Chien-Heng Lin, Sheng-Shing Lin in The Egyptian Journal of Neurology, Psychia… (2024)

  2. Article

    Open Access

    A Spacetime Odyssey of Neural Progenitors to Generate Neuronal Diversity

    To understand how the nervous system develops from a small pool of progenitors during early embryonic development, it is fundamentally important to identify the diversity of neuronal subtypes, decode the origi...

    Mengmeng Ge, Amirhossein Sheikhshahrokh, **ang Shi, Yu-Hong Zhang in Neuroscience Bulletin (2023)

  3. Article

    Open Access

    Therapeutic strategies for retention of cranioplasty titanium mesh after mesh exposure

    Titanium mesh exposure after cranioplasty is a possible complication and is usually managed by mesh removal and flap transfer, but the advantages of the rigid prosthesis are then lost. This study aimed to pres...

    Yao-Hua Zhao, Yu-Hong Feng, Hai-Tao Deng, Wei-Qi Huang, Li-Hong Xu in Acta Neurochirurgica (2022)

  4. Article

    Open Access

    Long-range GABAergic projections from the nucleus of the solitary tract

    The nucleus of the solitary tract (NTS) plays a crucial role in integrating peripheral information regarding visceral functions. Glutamate decarboxylase 2 (GAD2) inhibitory neurons are abundant in the NTS, and...

    Mei-Yu Shi, Lu-Feng Ding, Yu-Hong Guo, Yu-**ao Cheng, Guo-Qiang Bi in Molecular Brain (2021)

  5. Article

    Retraction Note to: Juvenile-onset myasthenia gravis: autoantibody status, clinical characteristics and genetic polymorphisms

    The Joint Editors-in-Chief have retracted this article [1] at the request of the University of Bergen and the Norwegian Board of Health Supervision.

    Yu Hong, Geir Olve Skeie, Paraskevi Zisimopoulou in Journal of Neurology (2019)

  6. Article

    Open Access

    Epileptic spasms in PPP1CB-associated Noonan-like syndrome: a case report with clinical and therapeutic implications

    Noonan syndrome-like disorder with loose anagen hair-2 (NSLH2) is an extremely rare disease caused by a heterozygous mutation in the PPP1CB gene on chromosome 2p23. The syndrome causes not only numerous dysmor...

    Chien-Heng Lin, Wei-De Lin, I-Ching Chou, Inn-Chi Lee, Hueng-Chuen Fan in BMC Neurology (2018)

  7. Article

    Open Access

    Interaction of basolateral amygdala, ventral hippocampus and medial prefrontal cortex regulates the consolidation and extinction of social fear

    Following a social defeat, the balanced establishment and extinction of aversive information is a beneficial strategy for individual survival. Abnormal establishment or extinction is implicated in the developm...

    Chu-Chu Qi, Qing-Jun Wang, Xue-zhu Ma, Hai-Chao Chen in Behavioral and Brain Functions (2018)

  8. Article

    Open Access

    p38 mediates mechanical allodynia in a mouse model of type 2 diabetes

    Painful Diabetic Neuropathy (PDN) affects more than 25% of patients with type 2 diabetes; however, the pathogenesis remains unclear due to lack of knowledge of the molecular mechanisms leading to PDN. In our c...

    Hsinlin T Cheng, Jacqueline R Dauch, Sang Su Oh, John M Hayes, Yu Hong in Molecular Pain (2010)