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Myotonic dystrophy types 1 and 2
Tetsuo Ashizawa,
Partha S. Sarkar
Neurology
Research output
:
Contribution to journal
›
Article
›
peer-review
70
Scopus citations
Overview
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Dive into the research topics of 'Myotonic dystrophy types 1 and 2'. Together they form a unique fingerprint.
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Keyphrases
Myotonic Dystrophy
100%
Myotonic Dystrophy Type 2
100%
Pathogenic Mechanism
50%
Multisystemic
50%
Expanded Repeats
50%
DNA Sequencing
25%
New Therapeutic Approaches
25%
RNA Transcripts
25%
Binding Site
25%
Disease Severity
25%
Sequestration
25%
Evidence Support
25%
Muscle Fiber
25%
Autosomal Dominant Disorder
25%
Inherited Disorders
25%
Chromatin Structure
25%
Supportive Therapy
25%
Congenital Disorders
25%
Gene Transcript
25%
Type II Fibers
25%
Mutant RNA
25%
CUG-binding Protein 1 (CUGBP1)
25%
Myotonia
25%
Repeat Size
25%
Short Tandem Repeat
25%
Repeated DNA
25%
Muscle Degeneration
25%
Gene Expression Dysregulation
25%
Biochemistry, Genetics and Molecular Biology
Binding Protein
100%
Gene Expression
100%
RNA
100%
Binding Site
100%
DNA Sequence
100%
Autosomal Dominant Inheritance
100%
Synapsin I
100%
Chromatin Structure
100%
Microsatellite DNA
100%
Neuroscience
Myotonic Dystrophy
100%
Protein Binding
33%
Gene Expression
33%
Epileptic Absence
33%
Binding Site
33%
Autosomal Dominant Disorder
33%
DNA Sequencing
33%
Muscle Atrophy
33%
Synapsin I
33%
Short Tandem Repeat
33%
Chromatin Structure
33%
Medicine and Dentistry
Myotonic Dystrophy
100%
Disease
40%
Gene Expression
20%
Protein Binding
20%
Epileptic Absence
20%
DNA Sequence
20%
Muscle Atrophy
20%
Binding Site
20%
Synapsin I
20%
Chromatin Structure
20%
Short Tandem Repeat
20%
Autosomal Dominant Disorder
20%
Myotonia
20%