K. Arita

发表

Gap junction development in the human fetal hair follicle and bulge region

J. R. McMillan, M. Akiyama, H. Shimizu, 2004, The British journal of dermatology.

Human bullous pemphigoid antigen 2 transgenic skin elicits specific IgG in wild-type mice.

M. Akiyama, H. Shimizu, E. Olasz, 2007, The Journal of investigative dermatology.

A novel mutation in the VDR gene in hereditary vitamin D‐resistant rickets

M. Akiyama, J. McGrath, V. Wessagowit, 2007, The British journal of dermatology.

Mutations in lipid transporter ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer.

J. R. McMillan, M. Akiyama, H. Shimizu, 2005, The Journal of clinical investigation.

Erythrokeratoderma variabilis without connexin 31 or connexin 30.3 gene mutation: immunohistological, ultrastructural and genetic studies.

M. Akiyama, H. Shimizu, T. Onozuka, 2003, Acta dermato-venereologica.

A novel GJB2 mutation p.Asn54His in a patient with palmoplantar keratoderma, sensorineural hearing loss and knuckle pads.

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

Complete remission of angiolymphoid hyperplasia with eosinophilia using topical tacrolimus

H. Shimizu, T. Nomura, S. Shinkuma, 2017, EJD. European journal of dermatology.

Deep venous thrombosis in patients with Behçet's disease

H. Shimizu, T. Nomura, K. Izumi, 2015, The Journal of dermatology.

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

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

Colocalization of kindlin-1, kindlin-2, and migfilin at keratinocyte focal adhesion and relevance to the pathophysiology of Kindler syndrome.

J. McGrath, S. Ussar, I. Hart, 2008, The Journal of investigative dermatology.

Changing pattern of deiminated proteins in developing human epidermis.

M. Akiyama, H. Shimizu, T. Senshu, 2003, The Journal of investigative dermatology.

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 .

Focal dermal hypoplasia resulting from a new nonsense mutation, p.E300X, in the PORCN gene.

J. McGrath, V. Wessagowit, J. Lai-Cheong, 2008, Journal of dermatological science.

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.

Genetic analysis of a novel splice‐site mutation in TMC8 reveals the in vivo importance of the transmembrane channel‐like domain of TMC8

H. Shimizu, T. Nomura, S. Shinkuma, 2016, The British journal of dermatology.

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.

Two cases of pyoderma gangrenosum complicated with nasal septal perforation

D. Inokuma, T. Yokota, H. Kobayashi, 1999, The British journal of dermatology.

Five new homozygous mutations in the KIND1 gene in Kindler syndrome.

Vinod K. Sharma, J. McGrath, R. Kumar, 2007, The Journal of investigative dermatology.

Intraepidermal neutrophilic IgA pemphigus successfully treated with dapsone.

H. Shimizu, T. Nomura, R. Abe, 2012, European journal of dermatology : EJD.

Unusual molecular findings in Kindler syndrome

J. McGrath, H. Fassihi, C. Pourreyron, 2007, The British journal of dermatology.

Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis

S. Tsai, J. McGrath, Ming-Wei Lin, 2010, European Journal of Human Genetics.

Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis.

M. Akiyama, H. Shimizu, J. McGrath, 2008, American journal of human genetics.

New insight into mechanisms of pruritus from molecular studies on familial primary localized cutaneous amyloidosis

J. McGrath, F. Palisson, M. Hide, 2009, The British journal of dermatology.

Familial primary localized cutaneous amyloidosis in Brazil.

J. McGrath, K. Arita, T. Sakuma, 2009, Archives of dermatology.

Two cases of atypical membranous aplasia cutis with hair collar sign: one with dermal melanocytosis, and the other with naevus flammeus

M. Akiyama, H. Shimizu, K. Yokota, 2005, Clinical and experimental dermatology.

Recurrence of hydroxyurea-induced leg ulcer after discontinuation of treatment.

M. Akiyama, H. Shimizu, K. Arita, 2011, Acta dermato-venereologica.

Patients with recessive dystrophic epidermolysis bullosa develop squamous-cell carcinoma regardless of type VII collagen expression.

J. McGrath, I. Leigh, H. Fassihi, 2007, The Journal of investigative dermatology.

Lichen planus in childhood showing various cutaneous features.

H. Shimizu, D. Inokuma, K. Arita, 2012, Acta dermato-venereologica.

Polymorphism of the MUC1 mucin gene is associated with susceptibility to lung adenocarcinoma and poor prognosis.

N. Kohno, A. Yokoyama, K. Kondo, 2005, Oncology reports.

Genetic diseases of junctions.

J. McGrath, J. Lai-Cheong, K. Arita, 2007, The Journal of investigative dermatology.

Changes in Gap Junction Distribution and Connexin Expression Pattern During Human Fetal Skin Development

J. R. McMillan, M. Akiyama, H. Shimizu, 2002, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Novel ABCA12 mutations identified in two cases of non-bullous congenital ichthyosiform erythroderma associated with multiple skin malignant neoplasia.

M. Akiyama, H. Shimizu, K. Natsuga, 2007, The Journal of investigative dermatology.

Severely hyperkeratotic erythroderma associated with Hodgkin's disease: does a high serum level of granulocyte-colony stimulating factor contribute to formation of skin lesions?

M. Akiyama, H. Shimizu, K. Arita, 2003, Journal of the American Academy of Dermatology.

Squamous cell carcinoma in a patient with non‐bullous congenital ichthyosiform erythroderma

M. Akiyama, H. Shimizu, K. Kodama, 2003, The British journal of dermatology.

Case of hereditary leiomyomatosis and renal cell cancer showing multiple cutaneous leiomyomas harboring a recurrent nonsense mutation in the fumarate hydratase gene

H. Ujiie, W. Nishie, K. Arita, 2021, The Journal of dermatology.

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.

Cutaneous metastasis of prostate carcinoma

H. Shimizu, H. Shimizu, K. Arita, 2002, Clinical and experimental dermatology.

Acral Peeling Skin Syndrome: A Clinically and Genetically Heterogeneous Disorder

J. McGrath, M. Medenica, K. Arita, 2012, Pediatric dermatology.

Generalized acute subcutaneous edema as a rare cutaneous manifestation of severe dermatomyositis

H. Shimizu, K. Natsuga, R. Abe, 2016, Journal of the European Academy of Dermatology and Venereology : JEADV.

Two cases of folliculosebaceous cystic hamartoma

H. Shimizu, R. Abe, H. Kawasaki, 2006, Clinical and experimental dermatology.

Lupus erythematosus profundus successfully treated with dapsone: review of the literature.

H. Shimizu, Miki Ito, H. Ujiie, 2006, Archives of dermatology.

Severe cholinergic urticaria successfully treated with scopolamine butylbromide in addition to antihistamines

H. Shimizu, T. Shimizu, K. Natsuga, 2006, Clinical and experimental dermatology.

Disappearing subcutaneous papules and nodules: Characteristic features of muscle herniation and piezogenic pedal papules

H. Shimizu, W. Nishie, K. Arita, 2017, The Journal of dermatology.

Severe subcutaneous hematoma in a patient with psoriatic arthritis: Changes of platelet count in psoriatic patients with biologic agents

H. Shimizu, H. Hata, Y. Fujita, 2017, The Journal of dermatology.

Novel mutation p.Gly59Arg in GJB6 encoding connexin 30 underlies palmoplantar keratoderma with pseudoainhum, knuckle pads and hearing loss

M. Akiyama, H. Shimizu, A. Ishiko, 2009, The British journal of dermatology.

A novel N14Y mutation in Connexin26 in keratitis-ichthyosis-deafness syndrome: analyses of altered gap junctional communication and molecular structure of N terminus of mutated Connexin26.

M. Akiyama, H. Shimizu, T. Aizawa, 2006, The American journal of pathology.

Nodular morphoea: a first case associated with linear morphoea

H. Shimizu, T. Nomura, K. Natsuga, 2016, EJD. European journal of dermatology.

Erythema annulare centrifugum-like neutrophilic dermatosis: effects of potassium iodide.

H. Shimizu, S. Shinkuma, K. Arita, 2012, Acta dermato-venereologica.

Nail deformity associated with hereditary multiple exostoses.

M. Akiyama, H. Shimizu, K. Arita, 2005, Journal of the American Academy of Dermatology.

The South African "bathing suit ichthyosis" is a form of lamellar ichthyosis caused by a homozygous missense mutation, p.R315L, in transglutaminase 1.

M. Akiyama, H. Shimizu, J. McGrath, 2007, Journal of Investigative Dermatology.

Large subcutaneous abscesses caused by Mycobacterium fortuitum infection.

H. Shimizu, K. Kodama, H. Ujiie, 2008, Acta dermato-venereologica.

Skin involvement in ALK-negative systemic anaplastic large-cell lymphoma.

H. Shimizu, T. Kondo, R. Abe, 2012, Journal of American Academy of Dermatology.

A case of squamous cell carcinoma presenting as a longstanding ulcer a recessive dystrophic epidermolysis bullosa patient

H. Shimizu, S. Aoyagi, H. Hata, 2013 .

Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis.

M. Akiyama, H. Shimizu, J. McGrath, 2008, American journal of human genetics.

Childhood subepidermal blistering disease with autoantibodies to type VII collagen and laminin‐332

M. Akiyama, H. Shimizu, K. Natsuga, 2011, The British journal of dermatology.