Morphology of Niemann-Pick type C metabolic storage disorder
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A white girl, born of nonconsanguineous parents at term by spontaneous vaginal delivery, developed neonatal hepatitis with jaundice at 2 months. Jaund
Lysosomal storage diseases Nature Reviews Disease Primers
Biophysical impact of sphingosine and other abnormal lipid accumulation in Niemann-Pick disease type C cell models - ScienceDirect
Lysosomal storage diseases Nature Reviews Disease Primers
Niemann–Pick Disease Type C: Induced Pluripotent Stem Cell–Derived Neuronal Cells for Modeling Neural Disease and Evaluating Drug Efficacy - Daozhan Yu, Manju Swaroop, Mengqiao Wang, Ulrich Baxa, Rongze Yang, Yiping Yan, Turhan
Pathophysiology of neuropathic lysosomal storage disorders - Bellettato - 2010 - Journal of Inherited Metabolic Disease - Wiley Online Library
IJMS, Free Full-Text
Frontiers Neuronopathic Gaucher disease: Beyond lysosomal dysfunction
Molecular mechanism(s) of neurodegeneration in Niemann-Pick type C disease - Ruđer Bošković Institute
Frontiers Lipid Involvement in Neurodegenerative Diseases of the Motor System: Insights from Lysosomal Storage Diseases
Disruptive lysosomal-metabolic signaling and neurodevelopmental deficits that precede Purkinje cell loss in a mouse model of Niemann-Pick Type-C disease
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Morphology of Niemann-Pick type C metabolic storage disorder
Adenosine A2A receptor stimulation restores cell functions and differentiation in Niemann-Pick type C-like oligodendrocytes
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