Pages that link to "Q42864281"

The following pages link to Temperature-Sensitive Phenotypes of Peroxisome-Assembly Processes Represent the Milder Forms of Human Peroxisome-Biogenesis Disorders (Q42864281):

Displaying 23 items.

• Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction (Q24291411) (← links)
• Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene (Q24293282) (← links)
• Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation (Q24532123) (← links)
• A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents (Q24613849) (← links)
• Catalase-less peroxisomes. Implication in the milder forms of peroxisome biogenesis disorder (Q28144608) (← links)
• PEX1 mutations in the Zellweger spectrum of the peroxisome biogenesis disorders (Q28266235) (← links)
• Identification of the molecular defect in patients with peroxisomal mosaicism using a novel method involving culturing of cells at 40 degrees C: implications for other inborn errors of metabolism (Q28270885) (← links)
• The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum (Q28293113) (← links)
• Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders (Q30168107) (← links)
• Genetic and molecular bases of peroxisome biogenesis disorders (Q34362011) (← links)
• Peroxisome biogenesis and human peroxisome-deficiency disorders (Q37670278) (← links)
• Novel mutations in the PEX2 gene of four unrelated patients with a peroxisome biogenesis disorder (Q38347768) (← links)
• The PEX1 ATPase Stabilizes PEX6 and Plays Essential Roles in Peroxisome Biology. (Q38733094) (← links)
• Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder (Q39638543) (← links)
• Inhibition of peroxisomal functions due to oxidative imbalance induced by mistargeting of catalase to cytoplasm is restored by vitamin E treatment in skin fibroblasts from Zellweger syndrome-like patients. (Q40482584) (← links)
• A novel pex2 mutant: catalase-deficient but temperature-sensitive PTS1 and PTS2 import (Q40726592) (← links)
• Formation of peroxisomes from peroxisomal ghosts in a peroxisome-deficient mammalian cell mutant upon complementation by protein microinjection (Q40914163) (← links)
• Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels (Q42036408) (← links)
• Redox Regulation of Homeostasis and Proteostasis in Peroxisomes. (Q46255766) (← links)
• Pex5p Imports Folded Tetrameric Catalase by Interaction with Pex13p (Q51758002) (← links)
• Peroxisome biogenesis disorders. (Q55209610) (← links)
• Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans (Q73668909) (← links)
• A PEX5 missense allele preferentially disrupts PTS1 cargo import into Arabidopsis peroxisomes (Q93004964) (← links)