K. Hojo

发表

Aberrant signature methylome by DNMT1 hot spot mutation in hereditary sensory and autonomic neuropathy 1E

J. Kocher, P. Dyck, S. Baheti, 2014, Epigenetics.

Mutations in DNMT 1 cause hereditary sensory neuropathy with dementia and hearing loss

J. Parisi, Yanhong Wu, M. Botuyan, 2016 .

Inflammatory glial activation in the brain of a patient with hereditary sensory neuropathy type 1 with deafness and dementia

K. Maeda, T. Kawamata, K. Hojo, 2004, Neuroscience Letters.

Defects of mutant DNMT1 are linked to a spectrum of neurological disorders.

G. Worrell, M. Grossman, W. Seeley, 2015, Brain : a journal of neurology.

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss

Elizabeth J. Atkinson, Douglas C. Wallace, Sumit Middha, 2011, Nature Genetics.

Expanded genetic insight and clinical experience of DNMT1-complex disorder

David T. Jones, J. Graff‐Radford, K. Maski, 2020, Neurology: Genetics.

Amyloid β Protein (25‐35) Phosphorylates MARCKS Through Tyrosine Kinase‐Activated Protein Kinase C Signaling Pathway in Microglia

Hideyuki Yamamoto, E. Miyamoto, N. Saito, 1999, Journal of neurochemistry.

Hereditary sensory neuropathy with deafness and dementia: a clinical and neuroimaging study

E. Mori, T. Imamura, M. Sasaki, 1999, European journal of neurology.

Congenital Myotonic Dystrophy: Molecular Diagnosis and Clinical Study

M. Fujimura, H. Yamagata, K. Hojo, 1995, American journal of perinatology.

PKC and tyrosine kinase involvement in amyloid β (25‐35)‐induced chemotaxis of microglia

M. Nakai, T. Kawamata, T. Hashimoto, 1998, Neuroreport.

Defects of mutant DNMT1 are linked to a spectrum of neurological disorders.

G. Worrell, W. Seeley, P. Dyck, 2015, Brain : a journal of neurology.