A new glucocerebrosidase-deficient neuronal cell model provides a tool to probe pathophysiology and therapeutics for Gaucher disease.
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Induced pluripotent stem cell models of lysosomal storage disorders.Acidic Ca2+ stores in neurodegeneration.Connecting Ca2+ and lysosomes to Parkinson disease.Neurodegenerative disease: models, mechanisms, and a new hope.Glucocerebrosidase haploinsufficiency in A53T α-synuclein mice impacts disease onset and course.Type 2 Gaucher disease in an infant despite a normal maternal glucocerebrosidase gene.
P2860
A new glucocerebrosidase-deficient neuronal cell model provides a tool to probe pathophysiology and therapeutics for Gaucher disease.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 19 May 2016
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
A new glucocerebrosidase-defic ...... rapeutics for Gaucher disease.
@en
A new glucocerebrosidase-defic ...... rapeutics for Gaucher disease.
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label
A new glucocerebrosidase-defic ...... rapeutics for Gaucher disease.
@en
A new glucocerebrosidase-defic ...... rapeutics for Gaucher disease.
@nl
prefLabel
A new glucocerebrosidase-defic ...... rapeutics for Gaucher disease.
@en
A new glucocerebrosidase-defic ...... rapeutics for Gaucher disease.
@nl
P2093
P2860
P50
P356
P1476
A new glucocerebrosidase-defic ...... erapeutics for Gaucher disease
@en
P2093
Amalia Dutra
An Hendrix
Bahafta Behre
Benoit Renvoise
Carole Cramer
Daniel S Ory
Edward I Ginns
Elma Aflaki
Evgenia Pak
Hideji Fujiwara
P2860
P304
P356
10.1242/DMM.024588
P577
2016-05-19T00:00:00Z