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Safety evaluation of a clinical focused ultrasound system for neuronavigation guided blood-brain barrier opening in non-human primates

Scientific reports, 2021-07, Vol.11 (1), p.15043-15043, Article 15043

2021

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Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage

Journal of human genetics, 2012-03, Vol.57 (3), p.202-206

2012

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Abnormal RNA structures (RNA foci) containing a penta-nucleotide repeat (UGGAA)n in the Purkinje cell nucleus is associated with spinocerebellar ataxia type 31 pathogenesis

Neuropathology, 2013-12, Vol.33 (6), p.600-611

2013

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Human Herpesvirus-6 corneal Endotheliitis after intravitreal injection of Ranibizumab

BMC ophthalmology, 2019-01, Vol.19 (1), p.19-19, Article 19

2019

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Elderly onset vitreous opacities as the initial manifestation in hereditary transthyretin (ATTR Val30Met) carries

Ophthalmic genetics, 2017-07, Vol.38 (4), p.387-391

2017

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Reduced brain-derived neurotrophic factor (BDNF) mRNA expression and presence of BDNF-immunoreactive granules in the spinocerebellar ataxia type 6 (SCA6) cerebellum

Neuropathology, 2012-12, Vol.32 (6), p.595-603

2012

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Cytoplasmic location of α1A voltage-gated calcium channel C-terminal fragment (Cav2.1-CTF) aggregate is sufficient to cause cell death

PloS one, 2013-03, Vol.8 (3), p.e50121

2013

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Pediatric brain repair from endogenous neural stem cells of the subventricular zone

Pediatric research, 2018-01, Vol.83 (1-2), p.385-396

2018

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Neuroregenerative and protective functions of Leukemia Inhibitory Factor in perinatal hypoxic-ischemic brain injury

Experimental neurology, 2020-08, Vol.330, p.113324-113324, Article 113324

2020

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Focused ultrasound enhanced intranasal delivery of brain derived neurotrophic factor produces neurorestorative effects in a Parkinson’s disease mouse model

Scientific reports, 2019-12, Vol.9 (1), p.19402-13, Article 19402

2019

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Unilateral Focused Ultrasound-Induced Blood-Brain Barrier Opening Reduces Phosphorylated Tau from The rTg4510 Mouse Model

Theranostics, 2019-01, Vol.9 (18), p.5396-5411

2019

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A BAC Transgenic Mouse Model of Spinocerebellar Ataxia Type 31 (SCA31) Manifests Late-Onset Motor Dysfunction and RNA Foci in Purkinje Cells (S43.007)

Neurology, 2013-02, Vol.80 (7_supplement)

2013

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A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation

Ophthalmic genetics, 2020-03, Vol.41 (2), p.175-182

2020

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Elderly onset vitreous opacities as the initial manifestation in hereditary transthyretin (ATTR Val30Met) carries

Ophthalmic genetics, 2017-08, Vol.38 (4), p.387

2017

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Cytoplasmic Location of [alpha]1A Voltage-Gated Calcium Channel C-Terminal Fragment

PloS one, 2013-03, Vol.8 (3), p.e50121

2013

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Cytoplasmic Location of [alpha]1A Voltage-Gated Calcium Channel C-Terminal Fragment Aggregate Is Sufficient to Cause Cell Death

PloS one, 2013-03, Vol.8 (3), p.e50121

2013

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Abnormal RNA structures ( RNA foci) containing a penta‐nucleotide repeat ( UGGAA ) n in the P urkinje cell nucleus is associated with spinocerebellar ataxia type 31 pathogenesis

Neuropathology, 2013-12, Vol.33 (6), p.600-611

2013

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Dissecting molecular mechanism of spinocerebellar ataxia type 31

Rinsho shinkeigaku = Clinical neurology, 2011, Vol.51 (11), p.1122-1124

2011

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Spinocerebellar ataxia type 31

Rinsho Shinkeigaku, 2010, Vol.50(11), pp.985-987

2010

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Spinocerebellar ataxia type 31

Rinshō shinkeigaku, 2010, Vol.50 (11), p.985-987

2010

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Magnetic Properties of Various Thick Co-Fe Circular Dot Arrays

Solid state phenomena, 2007-06, Vol.124-126, p.879-882

2007

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Molecular genetic approach to spinocerebellar ataxias

Rinsho Shinkeigaku, 2009, Vol.49(11), pp.907-909

2009

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Molecular genetic approach to spinocerebellar ataxias

Rinshō shinkeigaku, 2009, Vol.49 (11), p.907-909

2009

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Focused ultrasound stimulation of median nerve modulates somatosensory evoked responses

2019 IEEE International Ultrasonics Symposium (IUS), 2019, p.1085-1087

2019

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シンポジウム16―5　神経疾患とRNA　SCA31（脊髄小脳失調症31型）

臨床神経学, 2010, Vol.50(11), pp.985-987

2010

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Safety evaluation of a clinical focused ultrasound system for neuronavigation guided blood-brain barrier opening in non-human primates

Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage

Abnormal RNA structures (RNA foci) containing a penta-nucleotide repeat (UGGAA)n in the Purkinje cell nucleus is associated with spinocerebellar ataxia type 31 pathogenesis

Human Herpesvirus-6 corneal Endotheliitis after intravitreal injection of Ranibizumab

Elderly onset vitreous opacities as the initial manifestation in hereditary transthyretin (ATTR Val30Met) carries

Reduced brain-derived neurotrophic factor (BDNF) mRNA expression and presence of BDNF-immunoreactive granules in the spinocerebellar ataxia type 6 (SCA6) cerebellum

Cytoplasmic location of α1A voltage-gated calcium channel C-terminal fragment (Cav2.1-CTF) aggregate is sufficient to cause cell death

Pediatric brain repair from endogenous neural stem cells of the subventricular zone

Neuroregenerative and protective functions of Leukemia Inhibitory Factor in perinatal hypoxic-ischemic brain injury

Focused ultrasound enhanced intranasal delivery of brain derived neurotrophic factor produces neurorestorative effects in a Parkinson’s disease mouse model

Unilateral Focused Ultrasound-Induced Blood-Brain Barrier Opening Reduces Phosphorylated Tau from The rTg4510 Mouse Model

A BAC Transgenic Mouse Model of Spinocerebellar Ataxia Type 31 (SCA31) Manifests Late-Onset Motor Dysfunction and RNA Foci in Purkinje Cells (S43.007)

A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation

Elderly onset vitreous opacities as the initial manifestation in hereditary transthyretin (ATTR Val30Met) carries

Cytoplasmic Location of [alpha]1A Voltage-Gated Calcium Channel C-Terminal Fragment

Cytoplasmic Location of [alpha]1A Voltage-Gated Calcium Channel C-Terminal Fragment Aggregate Is Sufficient to Cause Cell Death

Abnormal RNA structures ( RNA foci) containing a penta‐nucleotide repeat ( UGGAA ) n in the P urkinje cell nucleus is associated with spinocerebellar ataxia type 31 pathogenesis

Dissecting molecular mechanism of spinocerebellar ataxia type 31

Spinocerebellar ataxia type 31

Spinocerebellar ataxia type 31

Magnetic Properties of Various Thick Co-Fe Circular Dot Arrays

Molecular genetic approach to spinocerebellar ataxias

Molecular genetic approach to spinocerebellar ataxias

Focused ultrasound stimulation of median nerve modulates somatosensory evoked responses

シンポジウム16―5　神経疾患とRNA　SCA31（脊髄小脳失調症31型）

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