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Human Dental Pulp-Derived Stem Cells Protect Against Hypoxic-Ischemic Brain Injury in Neonatal Mice

Stroke (1970), 2013-02, Vol.44 (2), p.551-554

2013

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The reciprocal regulation between mitochondrial-associated membranes and Notch signaling in skeletal muscle atrophy

eLife, 2023-12, Vol.12

2023

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Human dental pulp-derived stem cells promote locomotor recovery after complete transection of the rat spinal cord by multiple neuro-regenerative mechanisms

The Journal of clinical investigation, 2012-01, Vol.122 (1), p.80-90

2012

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The reciprocal regulation between mitochondrial-associated membranes and Notch signaling in skeletal muscle atrophy

eLife, 2023-12, Vol.12

2023

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Human dental pulp-derived stem cells promote locomotor recovery after complete transection of the rat spinal cord by multiple neuro-regenerative mechanisms

The Journal of clinical investigation, 2012-01, Vol.122 (1), p.80

2012

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Eosinophil counts can be a predictive marker of immune checkpoint inhibitor-induced secondary adrenal insufficiency: a retrospective cohort study

Scientific reports, 2022-01, Vol.12 (1), p.1294-1294, Article 1294

2022

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Identification of viral protein R of human immunodeficiency virus-1 (HIV) and interleukin-6 as risk factors for malignancies in HIV-infected individuals: A cohort study

PloS one, 2024-01, Vol.19 (1), p.e0296502-e0296502

2024

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Identification of a homozygous c.1039C>T (p.R347C) variant in CYP17A1 in a 67-year-old female patient with partial 17α-hydroxylase/17,20-lyase deficiency

Endocrine Journal, 2022, Vol.69(2), pp.115-120

2022

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Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation

Epilepsia (Copenhagen), 2013-07, Vol.54 (7), p.1282-1287

2013

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Zygotic Nuclear F-Actin Safeguards Embryonic Development

Cell reports (Cambridge), 2020-06, Vol.31 (13), p.107824, Article 107824

2020

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Exploring the Attitudes and Needs of Advance Care Planning Practice Among the Working Generation

Tokyo Women's Medical University Journal, 2022/12/20, Vol.6, pp.72-81

2022

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Identification of viral protein R of human immunodeficiency virus-1

PloS one, 2024-01, Vol.19 (1), p.e0296502

2024

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Maternal Chronic Disease and Congenital Anomalies of the Kidney and Urinary Tract in Offspring: A Japanese Cohort Study

American journal of kidney diseases, 2022-11, Vol.80 (5), p.619-628.e1

2022

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Investigation of the efficacy and adverse effects of lacosamide over 36 months

Epilepsy & behavior, 2023-07, Vol.144, p.109227-109227, Article 109227

2023

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Novel insights into presenilin 1 mutation associated with a distinctive dementia phenotype and cotton wool plaques

Neurological sciences, 2024-10, Vol.45 (10), p.4829-4835

2024

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Observation of mammalian living cells with femtosecond single pulse illumination generated by a soft X-ray free electron laser

Optica, 2024-06, Vol.11 (6), p.736

2024

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Impact of mental health on daily living activities of Japanese elderly

Preventive medicine, 2008-05, Vol.46 (5), p.457-462

2008

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Identification of a homozygous c.1039C>T (p.R347C) variant in CYP17A1 in a 67-year-old female patient with partial 17α-hydroxylase / 17,20-lyase deficiency

ENDOCRINE JOURNAL, 2022, Vol.69 (2), p.115-120

2022

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Leigh syndrome with spinal cord involvement due to a hemizygous NDUFA1 mutation

Brain & development (Tokyo. 1979), 2018-06, Vol.40 (6), p.498-502

2018

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Efficacy and safety associated with the infusion speed of intravenous immunoglobulin for the treatment of Kawasaki disease: a randomized controlled trial

Pediatric rheumatology online journal, 2021-07, Vol.19 (1), p.107-7, Article 107

2021

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Structural basis for CRMP2-induced axonal microtubule formation

Scientific reports, 2017-09, Vol.7 (1), p.10681-17, Article 10681

2017

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Identification of a homozygous c.1039C>T (p.R347C) variant in CYP17A1 in a 67-year-old female patient with partial 17α-hydroxylase/17,20-lyase deficiency

Endocrine Journal, 2021, pp.EJ21-0266

2021

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Association of cesarean birth with prevalence of functional constipation in toddlers at 3 years of age: results from the Japan Environment and Children’s Study (JECS)

BMC pediatrics, 2021-09, Vol.21 (1), p.1-419, Article 419

2021

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Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A

American journal of medical genetics. Part C, Seminars in medical genetics, 2014-09, Vol.166C (3), p.262-275

2014

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Expression analysis and mutation detection of DLX5 and DLX6 in autism

Brain & development (Tokyo. 1979), 2010-02, Vol.32 (2), p.98-104

2010

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Human Dental Pulp-Derived Stem Cells Protect Against Hypoxic-Ischemic Brain Injury in Neonatal Mice

The reciprocal regulation between mitochondrial-associated membranes and Notch signaling in skeletal muscle atrophy

Human dental pulp-derived stem cells promote locomotor recovery after complete transection of the rat spinal cord by multiple neuro-regenerative mechanisms

The reciprocal regulation between mitochondrial-associated membranes and Notch signaling in skeletal muscle atrophy

Human dental pulp-derived stem cells promote locomotor recovery after complete transection of the rat spinal cord by multiple neuro-regenerative mechanisms

Eosinophil counts can be a predictive marker of immune checkpoint inhibitor-induced secondary adrenal insufficiency: a retrospective cohort study

Identification of viral protein R of human immunodeficiency virus-1 (HIV) and interleukin-6 as risk factors for malignancies in HIV-infected individuals: A cohort study

Identification of a homozygous c.1039C>T (p.R347C) variant in CYP17A1 in a 67-year-old female patient with partial 17α-hydroxylase/17,20-lyase deficiency

Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation

Zygotic Nuclear F-Actin Safeguards Embryonic Development

Exploring the Attitudes and Needs of Advance Care Planning Practice Among the Working Generation

Identification of viral protein R of human immunodeficiency virus-1

Maternal Chronic Disease and Congenital Anomalies of the Kidney and Urinary Tract in Offspring: A Japanese Cohort Study

Investigation of the efficacy and adverse effects of lacosamide over 36 months

Novel insights into presenilin 1 mutation associated with a distinctive dementia phenotype and cotton wool plaques

Observation of mammalian living cells with femtosecond single pulse illumination generated by a soft X-ray free electron laser

Impact of mental health on daily living activities of Japanese elderly

Identification of a homozygous c.1039C>T (p.R347C) variant in CYP17A1 in a 67-year-old female patient with partial 17α-hydroxylase / 17,20-lyase deficiency

Leigh syndrome with spinal cord involvement due to a hemizygous NDUFA1 mutation

Efficacy and safety associated with the infusion speed of intravenous immunoglobulin for the treatment of Kawasaki disease: a randomized controlled trial

Structural basis for CRMP2-induced axonal microtubule formation

Identification of a homozygous c.1039C>T (p.R347C) variant in CYP17A1 in a 67-year-old female patient with partial 17α-hydroxylase/17,20-lyase deficiency

Association of cesarean birth with prevalence of functional constipation in toddlers at 3 years of age: results from the Japan Environment and Children’s Study (JECS)

Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A

Expression analysis and mutation detection of DLX5 and DLX6 in autism

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