THE BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION; RENO; ON BEHALF OF THE UNIVERSITY OF NEVADA
发明人:
BURKIN, DEAN,WUEBBLES, RYAN,VAN RY, PAM
申请号：
EP13827774
公开号：
EP2882447A4
申请日:
2013.08.09
申请国别(地区):
EP
年份:
2016
代理人:
摘要：
Disclosed herein are methods for diagnosing, prognosing and treating muscular dystrophy. The disclosed methods can be used to diagnosis, prognosis or treat a subject with merosin-deficient congenital muscular dystrophy Type 1A (MDC1A), limb-girdle muscular dystrophy (LGMD), facioscapulohumeral (FHMD), Beckers muscular dystrophy (BMD) or Duchenne muscular dystrophy (DMD). Also disclosed are methods of determining the effectiveness of an agent for the treatment of muscular dystrophy. In an example, a method of diagnosing or prognosing a subject with muscular dystrophy includes detecting expression of Galectin-1 or Galectin-3 in a sample obtained from the subject at risk of having or having one or more signs or symptoms associated with muscular dystrophy, thereby diagnosing or prognosing the subject with muscular dystrophy. Also provided are methods of enhancing muscle regeneration, repair, or maintenance in a subject by administering galectin, such as Galectin-1 and/or Galectin-3 to a subject in need thereof.
