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Recent advances in genetic analyses of oculocutaneous albinism types 2 and 4

Journal of dermatological science, 2008-07, Vol.51 (1), p.1-9

2008

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What is the novel clinical finding in dyschromatosis symmetrica hereditaria?

Journal of dermatology, 2013-01, Vol.40 (1), p.85-85

Tomita, Yasushi

2013

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Dyschromatosis Symmetrica Hereditaria and Aicardi-Goutières Syndrome 6 Are Phenotypic Variants Caused by ADAR1 Mutations

Journal of investigative dermatology, 2016-04, Vol.136 (4), p.875-878

2016

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Genetics of pigmentary disorders

American journal of medical genetics. Part C, Seminars in medical genetics, 2004-11, Vol.131C (1), p.75-81

2004

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Mutations of the RNA-Specific Adenosine Deaminase Gene (DSRAD) Are Involved in Dyschromatosis Symmetrica Hereditaria

American journal of human genetics, 2003-09, Vol.73 (3), p.693-699

2003

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The Efficacy and Safety of a Novel Extramedullary Guide Coordinated with 3D Surgical Assistive Software for Total Knee Arthroplasty: an Open-Label Single-Arm Trial

The Kurume Medical Journal, 2020/03/31, Vol.67(1), pp.31-40

2020

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CD19, a Response Regulator of B Lymphocytes, Regulates Wound Healing through Hyaluronan-Induced TLR4 Signaling

The American journal of pathology, 2009-08, Vol.175 (2), p.649-660

2009

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An Open-label Single-arm Trial of a Novel Extramedullary Guide Coordinated with 3D Surgical Assistive Software for Total Knee Arthroplasty

Acta medica Okayama, 2018-08, Vol.72 (4), p.441-445

2018

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Mechanism of the Inhibitory Effect of Tranexamic Acid on Melanogenesis in Cultured Human Melanocytes in the Presence of Keratinocyte-conditioned Medium

Journal of health science (Tokyo, Japan), 2007, Vol.53 (4), p.389-396

2007

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Primary cutaneous CD30 positive T-cell lymphoproliferative disorders with aberrant expression of PAX5: Report of three cases

Pathology international, 2012-04, Vol.62 (4), p.264-270

2012

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Questionnaire in patients with aborted sudden cardiac death due to coronary spasm in Japan

Heart and vessels, 2020-12, Vol.35 (12), p.1640-1649

2020

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An Open-Label, Single-Arm Study of a Patient-Specific Femoral Guide for Total Hip Arthroplasty via the Anterolateral Supine Approach, Linked with Three-Dimensional Surgical Support Software: Study Protocol

The Kurume Medical Journal, 2018/06/30, Vol.65(2), pp.71-75

2018

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Prediction of additional lymph node positivity and clinical outcome of micrometastases in sentinel lymph nodes in cutaneous melanoma: A multi-institutional study of 450 patients in Japan

Journal of dermatology, 2012-02, Vol.39 (2), p.130-137

2012

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Epidermal growth factor receptor tyrosine kinase inhibitors induce CCL2 and CCL5 via reduction in IL-1R2 in keratinocytes

Experimental dermatology, 2010-08, Vol.19 (8), p.730-735

2010

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Dyschromatosis symmetrica hereditaria associated with neurological disorders

Journal of dermatology, 2008-10, Vol.35 (10), p.662-666

2008

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Oculocutaneous Albinism Type 4 Is One of the Most Common Types of Albinism in Japan

American journal of human genetics, 2004-03, Vol.74 (3), p.466-471

2004

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Extrinsic compression of the left main coronary artery: A rare cause of cardiogenic shock

Radiology case reports, 2021-03, Vol.16 (3), p.714-717

2021

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Dyschromatosis symmetrica hereditaria by ADAR1 mutations and viral encephalitis: a hidden link?

International journal of dermatology, 2013-12, Vol.52 (12), p.1582-1584

2013

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Dermoscopic evaluation of vascular structures of various skin tumors in Japanese patients

Journal of dermatology, 2010-04, Vol.37 (4), p.316-322

2010

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Functional Analysis of Microphthalmia-associated Transcription Factor in Pigment Cell-specific Transcription of the Human Tyrosinase Family Genes

The Journal of biological chemistry, 1997-01, Vol.272 (1), p.503-509

1997

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LEDGF/DFS70, a Major Autoantigen of Atopic Dermatitis, Is a Component of Keratohyalin Granules

Journal of investigative dermatology, 2007-01, Vol.127 (1), p.75-80

2007

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Mutation Analysis of the ADAR1 Gene in Dyschromatosis Symmetrica Hereditaria and Genetic Differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis

Journal of investigative dermatology, 2005-06, Vol.124 (6), p.1186-1192

2005

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Effects of single therapeutic doses of promethazine, fexofenadine and olopatadine on psychomotor function and histamine-induced wheal- and flare-responses: a randomized double-blind, placebo-controlled study in healthy volunteers

Archives of Dermatological Research, 2012-05, Vol.304 (4), p.263-272

2012

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Nonuniform intensity distribution of the scattered light by moving diffuser across projection lens pupil and its influence in speckle reduction

Optical review (Tokyo, Japan), 2014, Vol.21 (1), p.90-93

2014

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Primary cutaneous T‐cell lymphoma of unspecified type with cytotoxic phenotype: Clinicopathological analysis of 27 patients

Cancer science, 2009-01, Vol.100 (1), p.33-41

2009

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Recent advances in genetic analyses of oculocutaneous albinism types 2 and 4

What is the novel clinical finding in dyschromatosis symmetrica hereditaria?

Dyschromatosis Symmetrica Hereditaria and Aicardi-Goutières Syndrome 6 Are Phenotypic Variants Caused by ADAR1 Mutations

Genetics of pigmentary disorders

Mutations of the RNA-Specific Adenosine Deaminase Gene (DSRAD) Are Involved in Dyschromatosis Symmetrica Hereditaria

The Efficacy and Safety of a Novel Extramedullary Guide Coordinated with 3D Surgical Assistive Software for Total Knee Arthroplasty: an Open-Label Single-Arm Trial

CD19, a Response Regulator of B Lymphocytes, Regulates Wound Healing through Hyaluronan-Induced TLR4 Signaling

An Open-label Single-arm Trial of a Novel Extramedullary Guide Coordinated with 3D Surgical Assistive Software for Total Knee Arthroplasty

Mechanism of the Inhibitory Effect of Tranexamic Acid on Melanogenesis in Cultured Human Melanocytes in the Presence of Keratinocyte-conditioned Medium

Primary cutaneous CD30 positive T-cell lymphoproliferative disorders with aberrant expression of PAX5: Report of three cases

Questionnaire in patients with aborted sudden cardiac death due to coronary spasm in Japan

An Open-Label, Single-Arm Study of a Patient-Specific Femoral Guide for Total Hip Arthroplasty via the Anterolateral Supine Approach, Linked with Three-Dimensional Surgical Support Software: Study Protocol

Prediction of additional lymph node positivity and clinical outcome of micrometastases in sentinel lymph nodes in cutaneous melanoma: A multi-institutional study of 450 patients in Japan

Epidermal growth factor receptor tyrosine kinase inhibitors induce CCL2 and CCL5 via reduction in IL-1R2 in keratinocytes

Dyschromatosis symmetrica hereditaria associated with neurological disorders

Oculocutaneous Albinism Type 4 Is One of the Most Common Types of Albinism in Japan

Extrinsic compression of the left main coronary artery: A rare cause of cardiogenic shock

Dyschromatosis symmetrica hereditaria by ADAR1 mutations and viral encephalitis: a hidden link?

Dermoscopic evaluation of vascular structures of various skin tumors in Japanese patients

Functional Analysis of Microphthalmia-associated Transcription Factor in Pigment Cell-specific Transcription of the Human Tyrosinase Family Genes

LEDGF/DFS70, a Major Autoantigen of Atopic Dermatitis, Is a Component of Keratohyalin Granules

Mutation Analysis of the ADAR1 Gene in Dyschromatosis Symmetrica Hereditaria and Genetic Differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis

Effects of single therapeutic doses of promethazine, fexofenadine and olopatadine on psychomotor function and histamine-induced wheal- and flare-responses: a randomized double-blind, placebo-controlled study in healthy volunteers

Nonuniform intensity distribution of the scattered light by moving diffuser across projection lens pupil and its influence in speckle reduction

Primary cutaneous T‐cell lymphoma of unspecified type with cytotoxic phenotype: Clinicopathological analysis of 27 patients

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