James R Mickelson Selected Research

Codon (Codons)

7/2004

Glycogen branching enzyme (GBE1) mutation causing equine glycogen storage disease IV.

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James R Mickelson Research Topics

Disease

9	Muscular Diseases (Myopathy) 02/2024 - 09/2002
3	Muscular Dystrophies (Muscular Dystrophy) 02/2024 - 01/2020
3	Rhabdomyolysis 12/2008 - 12/2002
2	Deglutition Disorders (Dysphagia) 02/2024 - 01/2021
2	Myositis (Idiopathic Inflammatory Myopathies) 02/2024 - 01/2019
2	Limb-Girdle Muscular Dystrophies (Limb-Girdle Muscular Dystrophy) 01/2023 - 01/2021
2	Glycogen Storage Disease Type IV (Andersen's Disease) 01/2009 - 04/2004
2	Glycogen Storage Disease (Glycogenosis) 05/2008 - 07/2004
2	Contracture 09/2005 - 12/2002
1	Hypertrophy 02/2024
1	Neuromuscular Diseases (Neuromuscular Disease) 02/2024
1	Myotonia Congenita (Thomsen Disease) 02/2024
1	Myotonia 02/2024
1	Muscular Atrophy (Muscle Atrophy) 02/2024
1	Communicable Diseases (Infectious Diseases) 11/2023
1	Atrophy 11/2023
1	Ganglion Cysts (Ganglion) 11/2023
1	Congenital Dyserythropoietic Anemia (Dyserythropoietic Anemia, Congenital) 11/2022
1	Urolithiasis 12/2021
1	Sarcoglycanopathies 01/2021
1	Myoglobinuria 01/2021
1	Nervous System Diseases (Neurological Disorders) 10/2020
1	Bethlem myopathy 01/2020
1	Scleroatonic muscular dystrophy 01/2020
1	Neuroaxonal Dystrophies (Neuroaxonal Dystrophy, Late Infantile) 01/2018
1	Leukoencephalopathies 01/2018
1	Horse Diseases (Horse Disease) 03/2014
1	Polyneuropathies (Polyneuropathy) 01/2013
1	Congenital Structural Myopathies (Centronuclear Myopathy) 08/2010
1	Paralysis (Palsy) 01/2009
1	Inborn Genetic Diseases (Disease, Hereditary) 01/2009
1	Asthenia 01/2009
1	Microsatellite Instability 09/2007
1	Genomic Instability 09/2007
1	Neoplasms (Cancer) 09/2007
1	Insulin Resistance 10/2004

Drug/Important Bio-Agent (IBA)

7	Polysaccharides (Glycans)IBA 03/2014 - 09/2002
3	Proteins (Proteins, Gene)FDA Link 01/2023 - 01/2019
2	Creatine Kinase (Creatine Phosphokinase)IBA 11/2023 - 01/2021
2	Sarcoglycans (beta Sarcoglycan)IBA 01/2023 - 01/2021
2	CollagenIBA 01/2023 - 01/2020
2	GlycogenIBA 05/2008 - 10/2004
2	CalciumIBA 08/2006 - 12/2002
2	Caffeine (No Doz)FDA LinkGeneric 09/2005 - 12/2002
2	1,4-alpha-Glucan Branching Enzyme (Glycogen Branching Enzyme)IBA 07/2004 - 04/2004
1	MyostatinIBA 02/2024
1	Phosphoric Diester Hydrolases (Phosphodiesterases)IBA 02/2024
1	Chloride Channels (Chloride Channel)IBA 02/2024
1	3',5'-Cyclic-AMP Phosphodiesterases (3',5' Cyclic Nucleotide Phosphodiesterase)IBA 02/2024
1	Laminin (Merosin)IBA 01/2023
1	DystrophinIBA 01/2023
1	Dystroglycans (Dystroglycan)IBA 01/2023
1	Nonsense Codon (Nonsense Mutation)IBA 11/2022
1	XanthineIBA 12/2021
1	aspartate-glutamate carrierIBA 01/2019
1	Glutamic Acid (Glutamate)FDA Link 01/2019
1	NAD (NADH)IBA 01/2018
1	myotubularinIBA 08/2010
1	N'-(3-aminopropyl)homospermidineIBA 01/2009
1	Glycogen Synthase (Synthase I)IBA 05/2008
1	AMP-Activated Protein KinasesIBA 10/2007
1	ParaffinIBA 09/2007
1	NucleotidesIBA 09/2007
1	Formaldehyde (Formol)FDA Link 09/2007
1	DNA (Deoxyribonucleic Acid)IBA 09/2007
1	Ryanodine Receptor Calcium Release Channel (Ryanodine Receptor)IBA 08/2006
1	L-Type Calcium Channels (Dihydropyridine Receptor)IBA 08/2006
1	Genetic Markers (Genetic Marker)IBA 08/2006
1	Sarcoplasmic Reticulum Calcium-Transporting ATPasesIBA 08/2006
1	Halothane (Fluothane)FDA Link 09/2005
1	EnzymesIBA 10/2004
1	Glucose (Dextrose)FDA LinkGeneric 10/2004
1	Codon (Codons)IBA 07/2004
1	Complementary DNA (cDNA)IBA 07/2004
1	Tyrosine (L-Tyrosine)FDA Link 07/2004

Therapy/Procedure

2	Therapeutics 02/2024 - 01/2013
1	Denervation 11/2023