Hideki Nakamura

发表

Superior Microvascular Perfusion of Infused Liposome-Encapsulated Hemoglobin Prior to Reductions in Infarctions after Transient Focal Cerebral Ischemia.

K. Houkin, K. Kazumata, Daisuke Shimbo, 2017, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Minodronate, a newly developed nitrogen-containing bisphosphonate, suppresses melanoma growth and improves survival in nude mice by blocking vascular endothelial growth factor signaling.

H. Shimizu, A. Yoshimura, R. Bucala, 2004, The American journal of pathology.

Overexpression of pigment epithelium-derived factor decreases angiogenesis and inhibits the growth of human malignant melanoma cells in vivo.

H. Shimizu, Tadamichi Shimizu, T. Imaizumi, 2004, The American journal of pathology.

Amelioration of dextran sulfate sodium-induced colitis by anti-macrophage migration inhibitory factor antibody in mice.

T. Iwanaga, M. Asaka, T. Sugiyama, 2002, Gastroenterology.

Cultured epidermal autografts from clinically revertant skin as a potential wound treatment for recessive dystrophic epidermolysis bullosa.

H. Shimizu, T. Nomura, Hideki Nakamura, 2019, The Journal of investigative dermatology.

Dominant and Recessive Compound Heterozygous Mutations in Epidermolysis Bullosa Simplex Demonstrate the Role of the Stutter Region in Keratin Intermediate Filament Assembly*

J. R. McMillan, H. Shimizu, Hideki Nakamura, 2002, The Journal of Biological Chemistry.

Regulation of human melanoma growth and metastasis by AGE-AGE receptor interactions.

H. Shimizu, Hideki Nakamura, S. Yamagishi, 2004, The Journal of investigative dermatology.

A Novel Active Mouse Model for Bullous Pemphigoid Targeting Humanized Pathogenic Antigen

M. Akiyama, H. Shimizu, Gang Wang, 2010, The Journal of Immunology.

Cas9‐guided haplotyping of three truncation variants in autosomal recessive disease

S. Fukushima, Hideki Nakamura, Y. Katsuda, 2022, Human mutation.

DNA-based prenatal exclusion of bullous congenital ichthyosiform erythroderma at the early stage, 10 to 11 weeks' of pregnancy, in two consequent siblings.

M. Akiyama, H. Shimizu, Hideki Nakamura, 2004, Journal of the American Academy of Dermatology.

Epitope-Dependent Pathogenicity of Antibodies Targeting a Major Bullous Pemphigoid Autoantigen Collagen XVII/BP180.

H. Shimizu, Hideki Nakamura, K. Natsuga, 2016, The Journal of investigative dermatology.

Molecular Pathogenesis of Genetic and Inherited Diseases Keratinocyte-/ Fibroblast-Targeted Rescue of Col 7 a 1-Disrupted Mice and Generation of an Exact Dystrophic Epidermolysis Bullosa Model Using a Human COL 7 A 1 Mutation

M. Akiyama, H. Shimizu, J. Uitto, 2010 .

Plectin Deficiency Leads to Both Muscular Dystrophy and Pyloric Atresia in Epidermolysis Bullosa Simplex

H. Shimizu, H. Osaka, Hideki Nakamura, 2010, Human mutation.

An annexin A1–FPR1 interaction contributes to necroptosis of keratinocytes in severe cutaneous adverse drug reactions

H. Shimizu, K. Nagao, C. Obuse, 2014, Science Translational Medicine.

Plectin expression patterns determine two distinct subtypes of epidermolysis bullosa simplex

J. R. McMillan, M. Akiyama, H. Shimizu, 2010, Human mutation.

CD44-Deficient Mice Do Not Exhibit Impairment of Epidermal Langerhans Cell Migration to Lymph Nodes after Epicutaneous Sensitization with Protein

M. Akiyama, H. Shimizu, Hideki Nakamura, 2010 .

Histochemical analysis of macrophage migration inhibitory factor in psoriasis vulgaris

H. Shimizu, Hideki Nakamura, R. Abe, 2002, Histochemistry and Cell Biology.

Clinical heterogeneity of 1649delG mutation in the tail domain of keratin 5: a Japanese family with epidermolysis bullosa simplex with mottled pigmentation.

H. Shimizu, Y. Horiguchi, Hideki Nakamura, 2005, The Journal of investigative dermatology.

DNA‐based prenatal diagnosis of plectin‐deficient epidermolysis bullosa simplex associated with pyloric atresia

J. R. McMillan, M. Akiyama, H. Shimizu, 2011, International journal of dermatology.

Possible involvement of exon 31 alternative splicing in phenotype and severity of epidermolysis bullosa caused by mutations in PLEC1.

J. R. McMillan, M. Akiyama, H. Shimizu, 2007, The Journal of investigative dermatology.

Epidermolysis bullosa simplex associated with pyloric atresia is a novel clinical subtype caused by mutations in the plectin gene (PLEC1).

J. R. McMillan, H. Shimizu, Tomohiko Nakamura, 2005, The Journal of molecular diagnostics : JMD.

Cutaneous marginal zone B-cell lymphoma: a case accompanied by massive plasmacytoid cells.

Hideki Nakamura, A. Ohkawara, T. Kiyohara, 2003, Journal of the American Academy of Dermatology.

A recurrent 'hot spot' glycine substitution mutation, G2043R in COL7A1, induces dominant dystrophic epidermolysis bullosa associated with intracytoplasmic accumulation of pro-collagen VII.

H. Shimizu, Hideki Nakamura, K. Natsuga, 2014, Journal of dermatological science.

Extracellular Vesicles from Amnion-Derived Mesenchymal Stem Cells Ameliorate Hepatic Inflammation and Fibrosis in Rats

K. Yuyama, Hideki Nakamura, N. Sakamoto, 2018, Stem cells international.

CTACK/CCL27 Accelerates Skin Regeneration via Accumulation of Bone Marrow‐Derived Keratinocytes

J. R. McMillan, H. Shimizu, Hideki Nakamura, 2006, Stem cells.

Revertant Mosaicism in Ichthyosis with Confetti Caused by a Frameshift Mutation in KRT1.

M. Akiyama, H. Shimizu, T. Nomura, 2016, The Journal of investigative dermatology.

Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA‐PLA1α in autosomal recessive hypotrichosis

M. Akiyama, H. Shimizu, J. Aoki, 2010, Human mutation.

Electron Microscopic and Immunohistochemical Findings of the Epidermal Basement Membrane in Two Families with Nail-patella Syndrome.

H. Shimizu, T. Nomura, Hideki Nakamura, 2019, Acta dermato-venereologica.

Antibody neutralization of TGF-β enhances the deterioration of collagen fascicles in a tissue-cultured tendon matrix with ex vivo fibroblast infiltration

H. Tohyama, Hideki Nakamura, K. Yasuda, 2007 .

Humanization of autoantigen

J. R. McMillan, M. Akiyama, H. Shimizu, 2007, Nature Medicine.

Complete paternal isodisomy of chromosome 17 in junctional epidermolysis bullosa with pyloric atresia.

M. Akiyama, H. Shimizu, Hideki Nakamura, 2010, The Journal of investigative dermatology.

Toxic epidermal necrolysis and Stevens-Johnson syndrome are induced by soluble Fas ligand.

H. Shimizu, Hideki Nakamura, R. Abe, 2003, The American journal of pathology.

Congenital nevi with hypomelanosis and fine scales

H. Shimizu, A. Kawada, Hideki Nakamura, 2019, European Journal of Dermatology.

Spindle cell angiosarcoma following irradiation therapy for cervical carcinoma

Hideki Nakamura, A. Ohkawara, K. Itoh, 2002, Journal of cutaneous pathology.

Tyrosinase gene analysis in Japanese patients with oculocutaneous albinism.

H. Shimizu, Hideki Nakamura, D. Sawamura, 2004, Journal of dermatological science.

Type XVII collagen coordinates proliferation in the interfollicular epidermis

F. Watt, H. Shimizu, Giacomo Donati, 2017, eLife.

Transarterial Regional Brain Hypothermia Inhibits Acute Aquaporin-4 Surge and Sequential Microvascular Events in Ischemia/Reperfusion Injury.

K. Houkin, K. Kazumata, Daisuke Shimbo, 2016, Neurosurgery.

Efficient Gene Reframing Therapy for Recessive Dystrophic Epidermolysis Bullosa with CRISPR/Cas9.

H. Shimizu, T. Nomura, Hideki Nakamura, 2019, The Journal of investigative dermatology.

Zonula occludens-1 demonstrates a unique appearance in buccal mucosa over several layers

H. Shimizu, Hideki Nakamura, K. Natsuga, 2021, Cell and Tissue Research.

Distribution of IL-18 and IL-18 receptor in human skin: various forms of IL-18 are produced in keratinocytes

H. Koizumi, K. Toyoshima, Hideki Nakamura, 2001, Archives of Dermatological Research.

Bullous Pemphigoid Autoantibodies Directly Induce Blister Formation without Complement Activation

H. Shimizu, Hideki Nakamura, K. Natsuga, 2014, The Journal of Immunology.

Complement Activation Induce Blister Formation without Bullous Pemphigoid Autoantibodies Directly

H. Shimizu, Hideki Nakamura, K. Natsuga, 2017 .

Extracellular cleavage of collagen XVII is essential for correct cutaneous basement membrane formation.

H. Shimizu, Hideki Nakamura, K. Natsuga, 2016, Human molecular genetics.

A founder effect of c.1938delC in ITGB4 underlies junctional epidermolysis bullosa and its application for prenatal testing

M. Akiyama, H. Shimizu, T. Kusaka, 2011, Experimental dermatology.

ITGB4 missense mutation in a transmembrane domain causes non-lethal variant of junctional epidermolysis bullosa with pyloric atresia.

H. Shimizu, Hideki Nakamura, H. Kawasaki, 2007, Journal of dermatological science.

Loss of interaction between plectin and type XVII collagen results in epidermolysis bullosa simplex

H. Shimizu, Hideki Nakamura, K. Natsuga, 2017, Human mutation.

COL7A1 mutation G2037E causes epidermal retention of type VII collagen

M. Akiyama, H. Shimizu, M. Furue, 2006, Journal of Human Genetics.

Hair follicle stem cell progeny heal blisters while pausing skin development

H. Shimizu, Yasuaki Kobayashi, Hideki Nakamura, 2020, bioRxiv.

Expression of exon-8-skipped kindlin-1 does not compensate for defects of Kindler syndrome.

H. Shimizu, M. Komine, Hideki Nakamura, 2011, Journal of dermatological science.

Kindler syndrome with severe intestinal involvement: a 31-year follow-up.

H. Shimizu, Hideki Nakamura, D. Inokuma, 2014, Acta dermato-venereologica.

A novel keratin 5 mutation in an African family with epidermolysis bullosa simplex indicates the importance of the amino acid located at the boundary site between the H1 and coil 1A domains.

M. Akiyama, H. Shimizu, Hideki Nakamura, 2013, Acta dermato-venereologica.

Context-Dependent Regulation of Collagen XVII Ectodomain Shedding in Skin.

H. Shimizu, Hideki Nakamura, K. Natsuga, 2015, The American journal of pathology.

A denatured collagen microfiber scaffold seeded with human fibroblasts and keratinocytes for skin grafting.

Y. Tabata, J. R. McMillan, H. Shimizu, 2011, Biomaterials.

Wnt/β-catenin signaling stabilizes hemidesmosomes in keratinocytes.

Hideki Nakamura, K. Natsuga, T. Tsukiyama, 2021, The Journal of investigative dermatology.

Novel COL7A1 mutation in a family with bullous dermolysis of the newborn: Phenotypic variability associated with a COL7A1 mutation within the same family

H. Shimizu, T. Nomura, Hideki Nakamura, 2018, The Journal of dermatology.

Hair follicle stem cell progeny heal blisters while pausing skin development

H. Shimizu, Yasuaki Kobayashi, Hideki Nakamura, 2020, bioRxiv.

Colocalization of Multiple Laminin Isoforms Predominantly beneath Hemidesmosomes in the Upper Lamina Densa of the Epidermal Basement Membrane

M. Akiyama, H. Shimizu, Hideki Nakamura, 2006, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Genetic studies of 20 Japanese families of dystrophic epidermolysis bullosa

H. Shimizu, Hideki Nakamura, D. Sawamura, 2005, Journal of Human Genetics.

A novel insertion mutation in COL7A1 identified in Hallopeau-Siemens recessive dystrophic epidermolysis bullosa.

H. Shimizu, Hideki Nakamura, D. Sawamura, 2003, Acta dermato-venereologica.

Cutaneous marginal zone B-cell lymphoma: a case accompanied by massive plasmacytoid cells.

Hideki Nakamura, A. Ohkawara, T. Kiyohara, 2003, Journal of the American Academy of Dermatology.

High expression of macrophage migration inhibitory factor in human melanoma cells and its role in tumor cell growth and angiogenesis.

M. Suzuki, Hideki Nakamura, R. Abe, 1999, Biochemical and biophysical research communications.

Genetic studies of 20 Japanese families of dystrophic epidermolysis bullosa

H. Shimizu, Hideki Nakamura, D. Sawamura, 2006, Journal of Human Genetics.

Cutaneous marginal zone B-cell lymphoma: a case accompanied by massive plasmacytoid cells.

Hideki Nakamura, A. Ohkawara, T. Kiyohara, 2003, Journal of the American Academy of Dermatology.

Specific Cutaneous Lesions of the Scalp in Myelodysplastic Syndrome with Deletion of 20q

Hideki Nakamura, T. Tarumi, A. Ohkawara, 1999, The Journal of dermatology.

Blockade of autoantibody-initiated tissue damage by using recombinant fab antibody fragments against pathogenic autoantigen.

H. Shimizu, H. Morioka, Gang Wang, 2010, The American journal of pathology.

A Novel Active Mouse Model for Bullous Pemphigoid Targeting Humanized Pathogenic Antigen

M. Akiyama, H. Shimizu, Gang Wang, 2010, Journal of Immunology.

Analysis of the COL17A1 in non-Herlitz junctional epidermolysis bullosa and amelogenesis imperfecta.

H. Shimizu, T. Ariga, Y. Sakiyama, 2006, International journal of molecular medicine.

Epitope-Dependent Pathogenicity of Antibodies Targeting a Major Bullous Pemphigoid Autoantigen Collagen XVII/BP180.

H. Shimizu, Hideki Nakamura, K. Natsuga, 2016, The Journal of investigative dermatology.