K. Nomura

发表

A homozygous nonsense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia.

J. McGrath, A. Christiano, W. Ahmad, 1999, The Journal of investigative dermatology.

A case of anti-nuclear antibody negative systemic lupus erythematosus associated with penile ulcer

K. Nomura, H. Yamabe, H. Osawa, 1993, Clinical Rheumatology.

Atrichia With Papular Lesions: Electron Microscopic Observations of Cystic Lesions

Masaaki Ito, K. Nomura, I. Hashimoto, 2001, The American Journal of dermatopathology.

Henoch-Schönlein Nephritis Manifesting with Purpura 15 years after Diagnosis of IgA Nephropathy

K. Nomura, H. Yamabe, M. Shimada, 2019, Case reports in nephrology.

Bullous pemphigoid antigen: cDNA cloning, cellular expression, and evidence for polymorphism of the human gene.

J. Uitto, A. Christiano, K. Nomura, 1990, The Journal of investigative dermatology.

Expression of the 67‐kDa elastin receptor in perforating  skin disorders

K. Nomura, S. Tajima, A. Matsushita, 2002, The British journal of dermatology.

In vivo transfer of a foreign gene to keratinocytes using the hemagglutinating virus of Japan-liposome method.

K. Tamai, K. Nomura, I. Hashimoto, 1997, The Journal of investigative dermatology.

A case report of siblings diagnosed with Papillon-Lefevre syndrome

T. Sugaya, M. Kawanami, K. Nomura, 2007 .

Papillon-Lefèvre syndrome: mutations and polymorphisms in the cathepsin C gene.

J. Uitto, L. Pulkkinen, K. Nomura, 2001, The Journal of investigative dermatology.

A keratin K10 gene mutation in a Japanese patient with epidermolytic hyperkeratosis

K. Tamai, K. Nomura, I. Hashimoto, 1997, Japanese Journal of Human Genetics.

L457F missense mutation within the 2B rod domain of keratin 9 in a Japanese family with epidermolytic palmoplantar keratoderma

K. Yoneda, N. Ito, K. Nomura, 2006, The British journal of dermatology.

A novel keratin K5 gene mutation in Dowling-Meara epidermolysis bullosa simplex.

H. Shimizu, T. Nishikawa, K. Tamai, 1996, The Journal of investigative dermatology.

Involvement of the AP-1 site within the 5′-flanking region of the stromelysin-1 gene in induction of the gene expression by UVA irradiation

J. Uitto, K. Tamai, A. Mauviel, 1996, Archives of Dermatological Research.

Clinical Criteria for Differentiating between Recessive and Dominant Forms of Dystrophic Epidermolysis Bullosa, Elaborated from an Analysis of 119 Cases

K. Nomura, I. Hashimoto, T. Imaizumi, 1993, The Journal of dermatology.

A Determination of Mutant Keratin Typing in Three Japanese Families with Hereditary Plamoplantar Keratoderma.

K. Nomura, D. Sawamura, Y. Mitsuhashi, 1995 .

Glycine substitution mutations in the type VII collagen gene (COL7A1) in dystrophic epidermolysis bullosa: implications for genetic counseling.

J. Uitto, J. McGrath, A. Christiano, 1997, The Journal of investigative dermatology.

Phenotypic heterogeneity in bullous congenital ichthyosiform erythroderma: possible somatic mosaicism for keratin gene mutation in the mildly affected mother of the proband.

K. Nomura, I. Hatayama, T. Kuronuma, 2001, Archives of dermatology.

A keratin K5 mutation (Leu 463→Pro) in a family with the Weber-Cockayne type of epidermolysis bullosa simplex

K. Tamai, K. Nomura, I. Hashimoto, 1997, Archives of Dermatological Research.

Type VII collagen DNA linkage analysis in a Japanese family with dominant dystrophic epidermolysis bullosa.

J. Uitto, K. Nomura, I. Hashimoto, 1994, Journal of dermatological science.

Bullous pemphigoid antigen (BPAG1): cDNA cloning and mapping of the gene to the short arm of human chromosome 6.

J. Uitto, M. Mattei, K. Nomura, 1990, Genomics.

Promoter/enhancer cassettes for keratinocyte gene therapy.

J. Miyazaki, K. Tamai, K. Nomura, 1999, The Journal of investigative dermatology.

Zosteriform Metastatic Skin Cancer: Report of Three Cases and Review of the Literature

K. Nomura, Y. Kikuchi, A. Matsuyama, 2001, Dermatology.

Epidermal Factors Stimulate Collagenase Synthesis by Epidermolysis Bullosa Fibroblasts

K. Nomura, I. Hashimoto, M. Takahashi, 1988, The Journal of dermatology.

Clinical Effects of Buten afine Hydrochloride (Mentax ®) on Tinea Superficialis

K. Nomura, I. Hashimoto, M. Shiraishi, 1994 .

Mouse 230-kDa bullous pemphigoid antigen gene: structural and functional characterization of the 5'-flanking region and interspecies conservation of the deduced amino-terminal peptide sequence of the protein.

J. Uitto, K. Tamai, K. Nomura, 1994, The Journal of investigative dermatology.

Novel SLC39A4 mutations in acrodermatitis enteropathica.

K. Nomura, K. Hanada, H. Nakano, 2003, The Journal of investigative dermatology.

Coexistence of Generalized Morphea with Histological Changes in Lichen Sclerosus et Atrophicus and Lichen Planus

K. Nomura, I. Hashimoto, D. Sawamura, 1998, The Journal of dermatology.

Epidermolysis bullosa with dysuria due to a cicatricial stricture of the preputial orifice.

K. Nomura, I. Hashimoto, S. Sato, 1984, Archives of dermatology.

Particular mutations in exon 85 of type VII collagen gene (COL7A1) induce severe itch : Specific glycine substitutions for dominant forms of epidermolysis bullosa pruriginosa

J. Uitto, K. Tamai, K. Nomura, 1998 .

Novel glycine substitution mutations in COL7A1 reveal that the Pasini and Cockayne-Touraine variants of dominant dystrophic epidermolysis bullosa are allelic.

J. Uitto, L. Pulkkinen, K. Nomura, 1997, The Journal of investigative dermatology.

Bilateral vermilion flap

K. Nomura, Y. Sawada, M. Ara, 1988 .

Bilateral vermilion flap. A modification of Goldstein's technique.

K. Nomura, Y. Sawada, M. Ara, 1988, International journal of oral and maxillofacial surgery.

A modification of Goldsteifis technique

Kazuo Nomura, Yukimasa Sawada, Michito Ara, 1988 .

Lentigo maligna melanoma with deep invasion along the mental nerve.

K. Nomura, I. Hashimoto, Y. Sawada, 1986, Journal of maxillofacial surgery.

Interleukin-1 induces collagenase production by recessive dystrophic epidermolysis bullosa fibroblasts

K. Tamai, K. Nomura, I. Hashimoto, 2004, Archives of Dermatological Research.

A study of the steroid sulfatase gene in families with X-linked ichthyosis using polymerase chain reaction.

K. Tamai, K. Nomura, I. Hashimoto, 1995, Acta dermato-venereologica.

Eccrine syringofibroadenomatosis in two patients with bullous pemphigoid.

K. Nomura, I. Hashimoto, Kazuo Nomura, 1997, Dermatology.

Eccrine syringofibroadenomatous hyperplasia in a patient with bullous pemphigoid: a case report and review of the literature.

K. Nomura, I. Hashimoto, Y. Katabira, 1991, Dermatologica.

Two cases of ichthyosis and their EPR analyses of stratum corneum

K. Nomura, Y. Matsuzaki, D. Sawamura, 2019, Journal of Cutaneous Immunology and Allergy.

Dominant dystrophic epidermolysis bullosa albopapuloidea Pasini -- ultrastructural observations of albopapuloid lesions and a type VII collagen DNA polymorphism study of a family.

K. Nomura, I. Hashimoto, D. Sawamura, 1997, Acta dermato-venereologica.

Expression of laminin, type IV procollagen and 230 kDa bullous pemphigoid antigen genes by keratinocytes and fibroblasts in culture: application of the polymerase chain reaction for detection of small amounts of messenger RNA

J. Uitto, K. Nomura, I. Hashimoto, 2004, Archives of Dermatological Research.

Solitary malignant schwannoma of the lower extremity a case report

K. Nomura, T. Narita, Y. Sawada, 1996, Clinical and experimental dermatology.

Rectal cancer associated with acquired hypertrichosis lanuginosa as a possible cutaneous marker of internal malignancy

K. Nomura, Y. Toyoki, M. Asano, 1998, Journal of Gastroenterology.

Recurrent COL7A1 mutations in Japanese patients with dystrophic epidermolysis bullosa: positional effects of premature termination codon mutations on clinical severity. Japanese Collaborative Study Group on Epidermolysis Bullosa.

H. Shimizu, T. Nishikawa, J. Uitto, 1999, The Journal of investigative dermatology.

Novel transglutaminase 1 gene mutations (R348X/Y365D) in a Japanese family with lamellar ichthyosis.

K. Yoneda, P. Steinert, K. Nomura, 2003, The Journal of investigative dermatology.

Effect of Cepharanthin on Superoxide Anion (O2–) Production by Macrophages

K. Nomura, I. Hashimoto, K. Hanada, 1988, The Journal of dermatology.

Incontinentia pigmenti in a male (XY) infant with long‐term follow up over 8 years

E. Ito, K. Nomura, Y. Matsuzaki, 2018, The Journal of dermatology.

Gene expression of collagenase and stromelysin in skin fibroblasts derived from dystrophic epidermolysis bullosa.

K. Nomura, I. Hashimoto, T. Sugawara, 1993, Journal of dermatological science.

Expression of collagenase and stromelysin in skin fibroblasts from recessive dystrophic epidermolysis bullosa

K. Nomura, I. Hashimoto, T. Sato, 2004, Archives of Dermatological Research.

Response of epidermolysis bullosa fibroblasts to factors derived from macrophages and polymorphonuclear leukocytes in terms of collagenase production.

K. Nomura, I. Hashimoto, D. Sawamura, 1988, Journal of Investigative Dermatology.

Interleukin-1 levels in blister fluids of some skin diseases with blister formation.

K. Nomura, I. Hashimoto, T. Imaizumi, 1990, Clinical physiology and biochemistry.