| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
American Journal of Pathology, Vol 133, 440-445, Copyright © 1988 by American Society for Investigative Pathology
REGULAR ARTICLES |
E Bonilla, B Schmidt, CE Samitt, AF Miranda, AP Hays, AB de Oliveira, HW Chang, S Servidei, E Ricci and DS Younger
Department of Neurology, College of Physicians & Surgeons, Columbia University, Columbia Presbyterian Medical Center, New York, New York.
Dystrophin is the gene product that is affected in Duchenne muscular dystrophy (DMD). Antibodies against dystrophin were used to study the protein in muscle fibers of carriers of the gene. The results showed that DMD carriers have normal and dystrophin-deficient fibers. Dystrophin immunohistochemistry may be helpful for the detection of DMD carriers.
This article has been cited by other articles:
![]() |
T. M. Suchyna and F. Sachs Mechanosensitive channel properties and membrane mechanics in mouse dystrophic myotubes J. Physiol., May 15, 2007; 581(1): 369 - 387. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Filosto, P. Tonin, G. Vattemi, L. Bertolasi, A. Simonati, N. Rizzuto, and G. Tomelleri The role of muscle biopsy in investigating isolated muscle pain Neurology, January 16, 2007; 68(3): 181 - 186. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. M. Hoogerwaard, I. B. Ginjaar, E. Bakker, and M. de Visser Dystrophin analysis in carriers of Duchenne and Becker muscular dystrophy Neurology, December 27, 2005; 65(12): 1984 - 1986. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.A. Witkowski Review Article: Dystrophin-Related Muscular Dystrophies J Child Neurol, October 1, 1989; 4(4): 251 - 271. [Abstract] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |