Creation of atopic dermatitis model mouse using double knock out mouse
Creation of atopic dermatitis model mouse using double knock out mouse
批准号:
22591240
负责人:
YONEDA Kozo
金额:
$3.33万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2010
资助国家:
日本
项目状态:
已结题
起止时间:
2010-04-01 至 2014-03-31
中文摘要
特应性皮炎是一种难治性皮肤病。该病的临床特征是瘙痒性湿疹。这种疾病现在是由微丝蛋白基因突变引起的。Loricrin是表皮角质细胞边缘带的主要成分。变异型Vohwinkel综合征的临床表现是伴有鱼鳞病的肢残性角化皮肤病。这种表型类似于寻常型鱼鳞病。寻常型鱼鳞病是由微丝蛋白基因的纯合或复合杂合突变引起的。本项目的目的是利用氯丙菊酯基因敲除小鼠建立特应性皮炎小鼠模型。
英文摘要
Atopic dermatitis is one of intractable skin diseases. The clinical feature of this disease is itchy eczema. This disease is caused by mutations in filaggrin gene now. Loricrin is major constituent of marginal band of epidermal corneocyte. The clinical aspects of the variant form of Vohwinkel syndrome are mutilating keratoderma with ichthyosis. This phenotype is similar to ichthyosis vulgaris. Ichthyosis vulgaris is caused by homozygous or compound heterozygous mutations in the filaggrin gene. The aim of this project is creation of atopic dermatitis mouse model using loricrin knock out mouse.
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DOI:
10.2340/00015555-1676
发表时间:
2014-03
期刊:
Acta dermato-venereologica
影响因子:
3.6
作者:
[K. Yoneda;T. Demitsu;M. Kakurai;T. Narita;K. Nakai;Y. Kubota;N. Ishii;T. Hashimoto]
通讯作者:
K. Yoneda;T. Demitsu;M. Kakurai;T. Narita;K. Nakai;Y. Kubota;N. Ishii;T. Hashimoto
Two cases of nevus sebaceous accompanying secondary tumors with Klothov expression
皮脂腺痣伴发Klothov表达继发性肿瘤2例
DOI:
10.1111/1346-8138.12371
发表时间:
2014
期刊:
J Dermatol
影响因子:
3.1
作者:
[Nakai K, Yoneda K, Haba R, Kushida Y, Katsuki N, Moriue J, Moriue T, Ishikawa E, Inoue S and Kubota Y]
通讯作者:
Inoue S and Kubota Y
Abnormally aggregated caveolin-1 in the cytoplasm of cellular model of classic Vohwinkel syndrome
经典 Vohwinkel 综合征细胞模型细胞质中异常聚集的 Caveolin-1
DOI:
--
发表时间:
2010
期刊:
影响因子:
--
作者:
[Yoneda K, Nakai K, Moriue T, Demitsu T and Kubota Y]
通讯作者:
Demitsu T and Kubota Y
Sphingosine 1‐phosphate attenuates peroxide‐induced apoptosis in HaCaT cells cultured in vitro
1-磷酸鞘氨醇减弱过氧化物诱导的体外培养 HaCaT 细胞凋亡
DOI:
--
发表时间:
2013
期刊:
Clincal and Experimental Dermatology
影响因子:
--
作者:
[T. Moriue, J. Igarashi, K. Yoneda, T. Hashimoto, K. Nakai, H. Kosaka, Y. Kubota]
通讯作者:
Y. Kubota
Consequences of two different amino-acid substitutions at the same codon in KRT14 indicate definitive roles of structural distortion in epidermolysis bullosa simplex pathogenesis
KRT14 中同一密码子的两个不同氨基酸取代的结果表明结构扭曲在单纯性大疱性表皮松解症发病机制中的明确作用
DOI:
--
发表时间:
2011
期刊:
J Invest Dermatol
影响因子:
6.5
作者:
[K.Natsuga, W.Nishie, et al.]
通讯作者:
et al.
共 15 条
Elucidation of pathophysiology or loricrin keratoderma
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批准号:18591250
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.82万
-
财政年份:2006
-
负责人:YONEDA Kozo
-
依托单位:
Study of pathophysiology of keratin disease
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批准号:14570796
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.24万
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财政年份:2002
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负责人:YONEDA Kozo
-
依托单位:
Construction of keratin disease keratinocyte model
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批准号:12670805
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.05万
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财政年份:2000
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负责人:YONEDA Kozo
-
依托单位:
Project of Hereditary Keratinizing Disorders
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批准号:10557079
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$4.29万
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财政年份:1998
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负责人:YONEDA Kozo
-
依托单位:
The expression of human loricrin gene
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批准号:07670947
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.47万
-
财政年份:1995
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负责人:YONEDA Kozo
-
依托单位:
海外基金