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Treatment of spinal muscular atrophy by sodium butyrate
Jan Gowth Chang
*
,
Hsiu Mei Hsieh-Li
, Yuh Jyh Jong
, Nancy M. Wang
, Chang Hai Tsai
, Hung Li
*
Corresponding author for this work
Research output
:
Contribution to journal
›
Article
›
peer-review
366
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Citations (Scopus)
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INIS
sodium
100%
atrophy
100%
motors
36%
neurons
36%
mice
36%
proteins
27%
diseases
18%
symptoms
18%
spinal cord
18%
exons
18%
humans
9%
correlations
9%
patients
9%
genes
9%
splicing
9%
in vivo
9%
birth
9%
drugs
9%
knock-out reactions
9%
oral administration
9%
lymphoid cells
9%
Neuroscience
Spinal Muscular Atrophy
100%
Butyric Acid
100%
Survival Motor Neuron Protein
30%
Spinal Cord
20%
Exon
20%
Motor Neuron
10%
In Vivo
10%
Cell Line
10%
Alternative Splicing
10%
Autosomal Recessive Disorder
10%
Muscle Atrophy
10%
Biochemistry, Genetics and Molecular Biology
Butyrate
100%
Survival of Motor Neuron
40%
Motor Neuron
40%
Exon
40%
SMN2
20%
Transgenics
20%
Alternative Splicing
20%
Birth Rate
20%
Autosomal Recessive Disorder
20%
Pharmacology, Toxicology and Pharmaceutical Science
Butyrate
100%
Spinal Muscular Atrophy
100%
Survival Motor Neuron Protein
30%
Diseases
10%
Disease Severity
10%
Oral Administration
10%
Muscle Atrophy
10%
Autosomal Recessive Disorder
10%
Paralysis
10%
Immunology and Microbiology
Autosomal Recessive Inheritance
50%
Birth Rate
50%
Anterior Horn Cell
50%
Lymphoid Cell Line
50%
Medicine and Dentistry
Motor Neuron
10%