Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,220,417 papers from all fields of science
Search
Sign In
Create Free Account
UTRN gene
Known as:
UTROPHIN
, UTRN
, DMDL
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
2 relations
UTRN protein, human
Utrophin
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2002
Highly Cited
2002
The carboxyterminus of the ATP-binding cassette transporter A1 interacts with a beta2-syntrophin/utrophin complex.
C. Buechler
,
A. Boettcher
,
S. M. Bared
,
Mario C O Probst
,
G. Schmitz
Biochemical and Biophysical Research…
2002
Corpus ID: 20611511
Review
2001
Review
2001
Pharmaceutical care research and education project: pharmacists' interventions.
R. Kassam
,
R. Kassam
,
+5 authors
A. Cave
Journal of the American Pharmacists Association
2001
Corpus ID: 8766714
Highly Cited
2000
Highly Cited
2000
Differential effects of dystrophin and utrophin gene transfer in immunocompetent muscular dystrophy (mdx) mice.
Satoru Ebihara
,
G. Guibinga
,
+5 authors
B. Petrof
Physiological Genomics
2000
Corpus ID: 1849186
Duchenne muscular dystrophy (DMD) is a fatal disease caused by defects in the gene encoding dystrophin. Dystrophin is a…
Expand
Highly Cited
2000
Highly Cited
2000
Immunolocalization of dystrobrevin in the astrocytic endfeet and endothelial cells in the rat cerebellum
H. Ueda
,
T. Baba
,
+5 authors
S. Ohno
Neuroscience Letters
2000
Corpus ID: 31284398
Highly Cited
1999
Highly Cited
1999
A second promoter provides an alternative target for therapeutic up-regulation of utrophin in Duchenne muscular dystrophy.
Edward A. Burton
,
J. Tinsley
,
Paul J. Holzfeind
,
Nanda R. Rodrigues
,
Kay E. Davies
Proceedings of the National Academy of Sciences…
1999
Corpus ID: 25512089
Duchenne muscular dystrophy (DMD) is an inherited muscle-wasting disease caused by the absence of a muscle cytoskeletal protein…
Expand
Highly Cited
1999
Highly Cited
1999
Utrophin Lacks the Rod Domain Actin Binding Activity of Dystrophin*
K. J. Amann
,
Athena W.-X. Guo
,
J. Ervasti
Journal of Biological Chemistry
1999
Corpus ID: 14986070
We previously identified a cluster of basic spectrin-like repeats in the dystrophin rod domain that binds F-actin through…
Expand
Highly Cited
1999
Highly Cited
1999
Discordant expression of utrophin and its transcript in human and mouse skeletal muscles.
A. Gramolini
,
G. Karpati
,
B. Jasmin
Journal of Neuropathology and Experimental…
1999
Corpus ID: 12254641
In order to determine the mechanisms regulating utrophin expression in human skeletal muscle, we examined the expression and…
Expand
Highly Cited
1998
Highly Cited
1998
Muscle and Neural Isoforms of Agrin Increase Utrophin Expression in Cultured Myotubes via a Transcriptional Regulatory Mechanism*
A. Gramolini
,
E. Burton
,
+6 authors
B. Jasmin
Journal of Biological Chemistry
1998
Corpus ID: 33124060
Duchenne muscular dystrophy is a prevalent X-linked neuromuscular disease for which there is currently no cure. Recently, it was…
Expand
Highly Cited
1995
Highly Cited
1995
Dystrophin-related Protein in the Platelet Membrane Skeleton
J. Earnest
,
G. F. Santos
,
Susanne Zuerbig
,
J. Fox
Journal of Biological Chemistry
1995
Corpus ID: 25171208
The platelet membrane is lined with a membrane skeleton that associates with transmembrane adhesion receptors and is thought to…
Expand
Highly Cited
1976
Highly Cited
1976
Functions of primary afferents and responses of extracellular K+ during spinal epileptiform seizures.
E. Lothman
,
G. Somjen
Electroencephalography and Clinical…
1976
Corpus ID: 4558781
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE