Shoji Wakasugi

Kumamoto University — Japan

Biochemistry, Genetics and Molecular Biology · Life Sciences

16h-index759citations33works0.02yr avg
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Research Topics

Amyloidosis: Diagnosis, Treatment, Outcomes(12), Skin and Cellular Biology Research(6), RNA and protein synthesis mechanisms(5), Trace Elements in Health(4), Coagulation, Bradykinin, Polyphosphates, and Angioedema(4)

Publications33 total

Immunohistochemical characterization of the cellular infiltrate in discoid lupus erythematosus
BioScience Trends·2011· 25 citedOpen Access
Immunohistochemical characterization of the cellular infiltrate in localized scleroderma
International Journal of Dermatology·2008· 29 cited
Two Cases of Anti-Epiligrin Cicatricial Pemphigoid With and Without Associated Malignancy
Acta Dermato Venereologica·2008· 27 citedOpen Access
Regulation of high molecular weight-melanoma associated antigen (HMW-MAA) gene expression by promoter DNA methylation in human melanoma cells
Oncogene·2005· 45 cited
Deterioration diagnosis by detection of partial discharge in a cable joint of 22 kV network
2005
Effect of the Intestinal Flora on Amyloid Deposition in a Transgenic Mouse Model of Familial Amyloidotic Polyneuropathy.
EXPERIMENTAL ANIMALS·2002· 24 citedOpen Access
Metastatic melanoma to the palatine tonsil with a favourable prognosis.
British Journal of Dermatology·2001· 28 cited
A novel nonsense mutation of the PEPD gene in a Japanese patient with prolidase deficiency
Journal of Human Genetics·2000· 19 citedOpen Access
CLINICAL, PATHOLOGICAL, IMMUNOHISTOCHEMICAL AND GENETIC DIFFERENCES BETWEEN MYCOSIS FUNGOIDES (MF) AND MF-LIKE ADULT T-CELL LYMPHOMA/LEUKEMIA(ATLL).
Journal of Acquired Immune Deficiency Syndromes & Human Retrovirology·1999
A Case of Superficial Leiomyosarcoma, and a Review of Japanese Cases
The Journal of Dermatology·1998· 4 cited
Clinical Phenotype of Bart's Syndrome Seen in a Family with Dominant Dystrophic Epidermolysis Bullosa
The Journal of Dermatology·1998· 9 cited
A novel isoform of the neurofibromatosis type-1 mRNA and a switch of isoforms during murine cell differentiation and proliferation
Gene·1994· 17 cited
Transgenic mouse model for human genetic diseases
Molecular Reproduction and Development·1993· 2 cited
Manipulating the Mouse Genome: New Approaches for the Dissection of Mouse Development
Development Growth & Differentiation·1991· 3 citedOpen Access
Systemic amyloidosis in transgenic mice carrying the human mutant transthyretin (Met30) gene. Pathologic similarity to human familial amyloidotic polyneuropathy, type I.
PubMed·1991· 68 citedOpen Access
Role of Serum Amyloid P Component for Systemic Amyloidosis in Transgenic Mice Carrying Human Mutant Transthyretin Gene
Gerontology·1991· 16 cited
Pathological Similarity of Transgenic Mice Carrying the Human Mutant Transthyretin Gene to Human Familial Amyloidotic Polyneuropathy (FAP) Type I
1991· 1 cited
Use of transgenic mice for dissecting the molecular mechanism of amyloid deposition in familial amyloidotic polyneuropathy
The Japanese Journal of Human Genetics·1990Open Access
Transgenic Mouse Model of an Autosomal Dominant Disease: Familial Amyloidotic Polyneuropathy
1990· 3 cited
Transgenic Mouse as Tools for the Study of Congenital Anomalies*
Congenital Anomalies·1989Open Access
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Frequent Co-authors

Kazunori Shimada(16), Shuichiro Maeda(12), Shigehiro Yi(9), T. Iwanaga(6), Hisayuki Nomiyama(5), Takeaki Inomoto(5), Ken‐ichi Yamamura(5), Teruhisa Tsuzuki(4), Masahiro Uehira(4), Kimi Araki(4), Jun‐ichi Miyazaki(4), Tomomichi Ono(4), K Yamamura(4), Fumi Tashiro(4), Makoto Fukuda(3), Kazuhiko Yamamura(3), Kiyoshi Takahashi(3), Hironobu Ihn(3), Ken‐Ichi Yamamura(3), Munekazu Naito(2)