23 results for author:"Oyama N." in Literature citations
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| Granulocyte colony-stimulating factor enhances arteriogenesis and ameliorates cerebral damage in a mouse model of ischemic stroke. Sugiyama Y., Yagita Y., Oyama N., Terasaki Y., Omura-Matsuoka E., Sasaki T., Kitagawa K. Stroke 42:770-775(2011) · Mapped (9) |
| SIK2 is a key regulator for neuronal survival after ischemia via TORC1-CREB. Sasaki T., Takemori H., Yagita Y., Terasaki Y., Uebi T., Horike N., Takagi H., Susumu T., Teraoka H., Kusano K. et al. Neuron 69:106-119(2011) · Mapped (15) |
| Lichen sclerosus et atrophicus-like skin lesions in a patient carrying a novel hydroxymethylbilane synthase mutation. Douderova D., Schneider-Yin X., Lautenschlager S., Saudek V., Theiler M., Hofbauer G.F., Dziunycz P.J., Oyama N., French L.E., Martasek P. et al. Blood Cells Mol. Dis. 45:176-179(2010) · Mapped (6) |
| Activation of NR2A receptors induces ischemic tolerance through CREB signaling. Terasaki Y., Sasaki T., Yagita Y., Okazaki S., Sugiyama Y., Oyama N., Omura-Matsuoka E., Sakoda S., Kitagawa K. J. Cereb. Blood Flow Metab. 30:1441-1449(2010) · Mapped (4) |
| Smooth muscle Notch1 mediates neointimal formation after vascular injury. Li Y., Takeshita K., Liu P.Y., Satoh M., Oyama N., Mukai Y., Chin M.T., Krebs L., Kotlikoff M.I., Radtke F. et al. Circulation 119:2686-2692(2009) · Mapped (7) |
| ECM1 interacts with fibulin-3 and the beta 3 chain of laminin 332 through its serum albumin subdomain-like 2 domain. Sercu S., Lambeir A.M., Steenackers E., El Ghalbzouri A., Geentjens K., Sasaki T., Oyama N., Merregaert J. |
| Deficiency of ROCK1 in bone marrow-derived cells protects against atherosclerosis in LDLR-/- mice. Wang H.W., Liu P.Y., Oyama N., Rikitake Y., Kitamoto S., Gitlin J., Liao J.K., Boisvert W.A. FASEB J. 22:3561-3570(2008) · Mapped (3) |
| A genomic and expression study of AP-1 in primary cutaneous T-cell lymphoma: evidence for dysregulated expression of JUNB and JUND in MF and SS. Mao X., Orchard G., Mitchell T.J., Oyama N., Russell-Jones R., Vermeer M.H., Willemze R., van Doorn R., Tensen C.P., Young B.D. et al. J. Cutan. Pathol. 35:899-910(2008) · Mapped (3) |
| ROCK1 mediates leukocyte recruitment and neointima formation following vascular injury. Noma K., Rikitake Y., Oyama N., Yan G., Alcaide P., Liu P.Y., Wang H., Ahl D., Sawada N., Okamoto R. et al. J. Clin. Invest. 118:1632-1644(2008) · Mapped (10) |
| Interaction of extracellular matrix protein 1 with extracellular matrix components: ECM1 is a basement membrane protein of the skin. Sercu S., Zhang M., Oyama N., Hansen U., Ghalbzouri A.E., Jun G., Geentjens K., Zhang L., Merregaert J.H. J. Invest. Dermatol. 128:1397-1408(2008) · Mapped (2) |
| Macrophage-derived chemokine (MDC)/CCL22 produced by monocyte derived dendritic cells reflects the disease activity in patients with atopic dermatitis. Hashimoto S., Nakamura K., Oyama N., Kaneko F., Tsunemi Y., Saeki H., Tamaki K. J. Dermatol. Sci. 44:93-99(2006) · Mapped (1) |
| Role of IL-12B promoter polymorphism in Adamantiades-Behcet's disease susceptibility: An involvement of Th1 immunoreactivity against Streptococcus Sanguinis antigen. Yanagihori H., Oyama N., Nakamura K., Mizuki N., Oguma K., Kaneko F. J. Invest. Dermatol. 126:1534-1540(2006) · Mapped (3) |
| Extracellular matrix protein 1 inhibits the activity of matrix metalloproteinase 9 through high-affinity protein/protein interactions. Fujimoto N., Terlizzi J., Aho S., Brittingham R., Fertala A., Oyama N., McGrath J.A., Uitto J. Exp. Dermatol. 15:300-307(2006) · UniProtKB (2) · Mapped (7) |
| Angiotensin converting enzyme inhibitors attenuated the expression of G-protein coupled receptor kinases in heart failure patients. Oyama N., Urasawa K., Kaneta S., Sakai H., Saito T., Takagi C., Yoshida I., Kitabatake A., Tsutsui H. Circ. J. 70:362-363(2006) · Mapped (6) |
| The wide distribution of endornaviruses, large double-stranded RNA replicons with plasmid-like properties. Fukuhara T., Koga R., Aoki N., Yuki C., Yamamoto N., Oyama N., Udagawa T., Horiuchi H., Miyazaki S., Higashi Y. et al. Arch. Virol. 151:995-1002(2006) · UniProtKB (8) |
| Decreased perivascular fibrosis but not cardiac hypertrophy in ROCK1+/- haploinsufficient mice. Rikitake Y., Oyama N., Wang C.Y., Noma K., Satoh M., Kim H.H., Liao J.K. Circulation 112:2959-2965(2005) · Mapped (3) |
| Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome. Ashton G.H., McLean W.H., South A.P., Oyama N., Smith F.J., Al-Suwaid R., Al-Ismaily A., Atherton D.J., Harwood C.A., Leigh I.M. et al. J. Invest. Dermatol. 122:78-83(2004) · Mapped (5) |
| Lack of association between the promoter polymorphisms at positions -308 and -238 of the tumor necrosis factor alpha gene and psoriasis vulgaris in Japanese patients. Tsunemi Y., Nishibu A., Saeki H., Oyama N., Nakamura K., Kishimoto M., Mitsui H., Tada Y., Torii H., Komine M. et al. Dermatology (Basel) 207:371-374(2003) · Mapped (6) |
| Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome. Siegel D.H., Ashton G.H.S., Penagos H.G., Lee J.V., Feiler H.S., Wilhelmsen K.C., South A.P., Smith F.J.D., Prescott A.R., Wessagowit V. et al. Am. J. Hum. Genet. 73:174-187(2003) · UniProtKB (1) |
| Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation. Hamada T., Wessagowit V., South A.P., Ashton G.H.S., Chan I., Oyama N., Siriwattana A., Jewhasuchin P., Charuwichitratana S., Thappa D.M. et al. J. Invest. Dermatol. 120:345-350(2003) · UniProtKB (1) · Mapped (1) |
| TGF-beta1-mediated regulation of thymus and activation-regulated chemokine (TARC/CCL17) synthesis and secretion by HaCaT cells co-stimulated with TNF-alpha and IFN-gamma. Zheng X., Nakamura K., Tojo M., Oyama N., Nishibu A., Satoh M., Kakinuma T., Wakugawa M., Tamaki K., Kaneko F. J. Dermatol. Sci. 30:154-160(2002) · Mapped (10) |
| Lack of association of TNF-238A and -308A in Japanese patients with psoriasis vulgaris, psoriatic arthritis and generalized pustular psoriasis. Nishibu A., Oyama N., Nakamura K., Kaneko F. J. Dermatol. Sci. 29:181-184(2002) · Mapped (6) |
| Novel point mutations in the steroid sulfatase gene in patients with X-linked ichthyosis: transfection analysis using the mutated genes. Oyama N., Satoh M., Iwatsuki K., Kaneko F. J. Invest. Dermatol. 114:1195-1199(2000) · UniProtKB (1) |