Bailee N Kain Selected Research

Glycogen Storage Disease XIV

1/2017	Asp263 missense variants perturb the active site of human phosphoglucomutase 1.
4/2016	Induced Structural Disorder as a Molecular Mechanism for Enzyme Dysfunction in Phosphoglucomutase 1 Deficiency.
11/2014	Compromised catalysis and potential folding defects in in vitro studies of missense mutants associated with hereditary phosphoglucomutase 1 deficiency.

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Bailee N Kain Research Topics

Disease

3	Glycogen Storage Disease XIV 01/2017 - 11/2014
1	Glycogen Storage Disease (Glycogenosis) 04/2016
1	Congenital, Hereditary, and Neonatal Diseases and Abnormalities (Congenital Disorders) 04/2016
1	Dilated Cardiomyopathy (Cardiomyopathy, Congestive) 11/2014

Drug/Important Bio-Agent (IBA)

2	EnzymesIBA 04/2016 - 11/2014
2	Proteins (Proteins, Gene)FDA Link 04/2016 - 11/2014
1	Amino Acids FDA Link 01/2017
1	PhosphoglucomutaseIBA 11/2014
1	Glucose (Dextrose)FDA LinkGeneric 11/2014
1	Complement System Proteins (Complement)IBA 11/2014

Therapy/Procedure

1	Precision Medicine 04/2016