Lejin Wang Selected Research

1 Autosomal Dominant Coronary Artery Disease

11/2003

Mutation of MEF2A in an inherited disorder with features of coronary artery disease.

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Lejin Wang Research Topics

Disease

2	Movement Disorders (Movement Disorder) 01/2020 - 07/2005
2	Retinitis Pigmentosa (Pigmentary Retinopathy) 09/2003 - 04/2002
1	Graves Ophthalmopathy 12/2020
1	Congenital Nystagmus 01/2020
1	Myopia 01/2019
1	X-Linked Infantile Nystagmus 11/2016
1	Blindness (Hysterical Blindness) 05/2016
1	Cataract (Cataracts) 05/2016
1	Coloboma (Colobomas) 01/2012
1	Marfan Syndrome (Marfan's Syndrome) 01/2012
1	Cardiovascular Diseases (Cardiovascular Disease) 12/2008
1	Leber Hereditary Optic Atrophy (Leber's Hereditary Optic Neuropathy) 06/2008
1	Ocular Albinism 01/2007
1	Generalized Epilepsy and Paroxysmal Dyskinesia 07/2005
1	Epilepsy (Aura) 07/2005
1	Channelopathies 07/2005
1	1 Autosomal Dominant Coronary Artery Disease 11/2003

Drug/Important Bio-Agent (IBA)

2	G-Protein-Coupled Receptors (Receptors, G Protein Coupled)IBA 11/2016 - 01/2007
1	6-methyladenineIBA 12/2020
1	RNA (Ribonucleic Acid)IBA 12/2020
1	N-methyladenosineIBA 12/2020
1	Qa-SNARE Proteins (Syntaxin)IBA 01/2020
1	Therapeutic UsesIBA 01/2019
1	RNA Splice SitesIBA 05/2016
1	Crystallins (Crystallin)IBA 05/2016
1	MorpholinosIBA 01/2012
1	ATP-Binding Cassette Transporters (ABC Transporters)IBA 01/2012
1	Adenosine Triphosphate (ATP)IBA 01/2012
1	Fibrillin-1IBA 01/2012
1	Messenger RNA (mRNA)IBA 12/2008
1	Mitochondrial DNA (mtDNA)IBA 06/2008
1	PotassiumIBA 07/2005
1	CalciumIBA 07/2005
1	Large-Conductance Calcium-Activated Potassium Channels (Maxi-K Channels)IBA 07/2005
1	MEF2 Transcription FactorsIBA 11/2003
1	Amino Acids FDA Link 11/2003
1	RNA Precursors (Precursor, mRNA)IBA 09/2003
1	Rhodopsin (Visual Purple)IBA 04/2002

Therapy/Procedure

1	Telescopes 01/2020