Pages that link to "Q41660586"
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The following pages link to Phenotypic heterogeneity in cultured skin fibroblasts from patients with disorders of peroxisome biogenesis belonging to the same complementation group (Q41660586):
Displaying 11 items.
- Presence of cytoplasmic factors functional in peroxisomal protein import implicates organelle-associated defects in several human peroxisomal disorders (Q33908619) (← links)
- Human peroxisomal disorders (Q34196103) (← links)
- Liver pathology and immunocytochemistry in congenital peroxisomal diseases: a review (Q36930280) (← links)
- Evidence that photodynamic stress kills Zellweger fibroblasts by a nonapoptotic mechanism (Q41049552) (← links)
- Diagnostic work-up of a peroxisomal patient (Q41366931) (← links)
- Resistance to erucic acid as a selectable marker for peroxisomal activity: isolation of revertants of an infantile Refsum disease cell line (Q41506888) (← links)
- Differential protein import deficiencies in human peroxisome assembly disorders (Q41920716) (← links)
- Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels (Q42036408) (← links)
- Peroxisome mosaicism in the livers of peroxisomal deficiency patients (Q49167581) (← links)
- Diagnosis and follow-up of a case of peroxisomal disorder with peroxisomal mosaicism (Q55989778) (← links)
- Morphometry of peroxisomes and immunolocalization of peroxisomal proteins in the liver of patients with generalised peroxisomal disorders (Q71607103) (← links)