Title:
マルファン症候群の分析のためのプローブの使用、スクリーニング方法およびキット
Document Type and Number:
Japanese Patent JP4706193
Kind Code:
B2
Abstract:
The purpose of this invention is to provide a probe for diagnosis of Marfan syndrome, which enables early diagnosis of Marfan syndrome, and to provide a method for screening using said probe. The invention is a probe for a Marfan Syndrome characterized by using a nucleic acid comprising following (a) or (b);
(a) a nucleic acid comprising a base sequence represented by base numbers 1-180000 shown in SEQ ID No. 1 of the sequence listing, or
(b) a nucleic acid in which a part of the base sequence of said base numbers 1-180000 is deleted, substituted or added, and having 80% homology with said base sequence.
Inventors:
Shinkawa Shinobu
Naomichi Matsumoto
Catherine Voileux
Guenale Bilaud
Guram Jong Do
Naomichi Matsumoto
Catherine Voileux
Guenale Bilaud
Guram Jong Do
Application Number:
JP2004158099A
Publication Date:
June 22, 2011
Filing Date:
May 27, 2004
Export Citation:
Assignee:
National University Corporation Nagasaki University
Institut National de la Sant'Edera Les Cheryche Medical
Institut National de la Sant'Edera Les Cheryche Medical
International Classes:
C12Q1/68; G01N33/50; A61K45/00; A61P19/04; C07K14/47; C12N15/09; G01N33/15; G01N33/53; G01N33/566
Domestic Patent References:
| JP7501212A |
Other References:
Database DDBJ/EMBL/GenBank [online], Accessin No. AC096921, 26-JAN-2002 uploaded, [retrieved on 2010-03-01]Definition: Homo sapiens chromosome 3 clone RP11-1024P17, complete sequence.
Attorney, Agent or Firm:
Kosaku Sugimura
Hiroshi Tokunaga
Shiro Fujitani
Kiyoshi Kuruma
Kenjiro Oyama
Kazuyuki Tomita
Hiroshi Tokunaga
Shiro Fujitani
Kiyoshi Kuruma
Kenjiro Oyama
Kazuyuki Tomita