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A new glucocerebrosidase-deficient neuronal cell model provides a tool to probe pathophysiology and therapeutics for Gaucher disease
by
Westbroek, Wendy
,
Nguyen, Matthew
,
Siebert, Marina
,
Lindstrom, Taylor
,
Burnett, Robert A
,
Aflaki, Elma
,
Jung, Olive
,
Tamargo, Rafael
,
Rodriguez-Gil, Jorge L
,
Acosta, Walter
,
Hendrix, An
,
Behre, Bahafta
,
Tayebi, Nahid
,
Fujiwara, Hideji
,
Sidhu, Rohini
,
Renvoise, Benoit
,
Ginns, Edward I
,
Dutra, Amalia
,
Pak, Evgenia
,
Cramer, Carole
,
Ory, Daniel S
,
Pavan, William J
,
Sidransky, Ellen
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Disease models & mechanisms
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Disease Models & Mechanisms
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Adenosine Triphosphate - Metabolism
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Animals
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Antibodies
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Antigens, Polyomavirus Transforming - Metabolism
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Calcium - Metabolism
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Cd24 Antigen - Metabolism
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Cell Biology
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Cell Culture
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Cell Line, Transformed
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Cells, Cultured
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Enzymes
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Gaucher Disease
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Gaucher Disease - Enzymology
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Gaucher Disease - Physiopathology
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Gaucher Disease - Therapy
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Gene Expression
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Genotype & Phenotype
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Glucocerebrosidase
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Glucosylceramidase - Deficiency
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Glucosylceramidase - Metabolism
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