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Mutation-Directed Therapeutics for Neurofibromatosis Type I
Andre Leier
, David M Bedwell
, Ann T Chen
, George Dickson
, Kim M Keeling
, Robert A Kesterson
, Bruce R Korf
, Tatiana T Marquez Lago
, Ulrich F Müller
, Linda Popplewell
, Jiangbing Zhou
, Deeann Wallis
SHLS Allied Health Professions
Research output
:
Contribution to journal
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Review article
›
peer-review
185
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Keyphrases
Neurofibromatosis Type I
100%
Neurofibromatosis Type 1 (NF-1)
100%
Genetic Disease
66%
Neurofibromin
66%
Direct Therapy
66%
Biotechnology
33%
Clinical Trials
33%
Regulatory Bodies
33%
Complementary DNA (cDNA)
33%
Therapeutic Approaches
33%
Tumor Suppressor
33%
Loss Function
33%
DNA Repair
33%
Exon Skipping
33%
Antisense Oligonucleotides
33%
Skin Spot
33%
Skeletal Dysplasia
33%
Potential Power
33%
RNA Repair
33%
Non-maximum Suppression
33%
Viral Vectors
33%
Nervous System Tumors
33%
Oligonucleotide Therapeutics
33%
Viral Nanoparticles
33%
Drug Regulatory
33%
RAS Pathway
33%
CRISPR Activation
33%
Therapeutic Procedure
33%
Medicine and Dentistry
Neurofibromatosis Type I
100%
Genetic Disorder
66%
Clinical Trial
33%
Signal Transduction
33%
Hope
33%
DNA Repair
33%
Exon Skipping
33%
Complementary DNA
33%
Antisense Oligonucleotide
33%
Virus Vector
33%
Clustered Regularly Interspaced Short Palindromic Repeat
33%
RNA Repair
33%
Nervous System Tumor
33%
Bone Dysplasia
33%
Ras Signaling
33%
Tumor Suppressor Protein
33%
Nanoparticle
33%
Diseases
33%
Pharmacology, Toxicology and Pharmaceutical Science
Neurofibromatosis Type 1
100%
Genetic Disorder
66%
Neurofibromin
66%
Nanoparticle
33%
Clinical Trial
33%
Tumor Suppressor Protein
33%
Bone Dysplasia
33%
Viral Vector
33%
Nervous System Tumor
33%
Antisense Oligonucleotide
33%
Complementary DNA
33%
Diseases
33%