Morphology of Niemann-Pick type C metabolic storage disorder
Por um escritor misterioso
Last updated 22 setembro 2024
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—the horizon expands
Models to study basic and applied aspects of lysosomal storage disorders - ScienceDirect
Comparative Hippocampal Proteome and Phosphoproteome in a Niemann–Pick, Type C1 Mouse Model Reveal Insights into Disease Mechanisms
Cells, Free Full-Text
Lysosomal Storage Diseases - Joseph Alroy, Jeremiah A. Lyons, 2014
Indian Pediatrics - Editorial
TPC2 rescues lysosomal storage in mucolipidosis type IV, Niemann–Pick type C1, and Batten disease
Niemann–Pick disease, type C - Wikipedia
Finding pathogenic commonalities between Niemann-Pick type C and other lysosomal storage disorders: Opportunities for shared therapeutic interventions - ScienceDirect
Lipid trafficking defects in Niemann-Pick type C disease
TPC2 rescues lysosomal storage in mucolipidosis type IV, Niemann–Pick type C1, and Batten disease
Glycosphingolipid catabolism and associated lysosomal storage diseases.
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