Pages that link to "Q67653760"
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The following pages link to Pathology of hepatic peroxisomes and mitochondria in patients with peroxisomal disorders (Q67653760):
Displaying 27 items.
- Pmp27 promotes peroxisomal proliferation (Q27934104) (← links)
- Mitochondrial alterations caused by defective peroxisomal biogenesis in a mouse model for Zellweger syndrome (PEX5 knockout mouse) (Q28360949) (← links)
- Absence of peroxisomes in mouse hepatocytes causes mitochondrial and ER abnormalities (Q28508098) (← links)
- Analysis of the putative role of 24‐carbon polyunsaturated fatty acids in the biosynthesis of docosapentaenoic (22:5n‐6) and docosahexaenoic (22:6n‐3) acids (Q28647102) (← links)
- Very large peroxisomes in distinct peroxisomal disorders (rhizomelic chondrodysplasia punctata and acyl-CoA oxidase deficiency): novel data. (Q31112558) (← links)
- Human peroxisomal disorders (Q34196103) (← links)
- Biochemistry of peroxisomes in health and disease (Q34418889) (← links)
- On the molecular etiology of decreased arachidonic (20:4n-6), docosapentaenoic (22:5n-6) and docosahexaenoic (22:6n-3) acids in Zellweger syndrome and other peroxisomal disorders (Q34738513) (← links)
- Autopsy findings in two siblings with infantile Refsum disease (Q35313752) (← links)
- Carbohydrate metabolism is perturbed in peroxisome-deficient hepatocytes due to mitochondrial dysfunction, AMP-activated protein kinase (AMPK) activation, and peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α) suppression (Q35604967) (← links)
- Congenital brain malformations in mitochondrial disease (Q36114824) (← links)
- Liver pathology and immunocytochemistry in congenital peroxisomal diseases: a review (Q36930280) (← links)
- Bile acids: the role of peroxisomes (Q37382119) (← links)
- Liver and chorion cytochemistry (Q38481677) (← links)
- Very long chain fatty acids in higher animals--a review (Q40531407) (← links)
- Practical guide for morphometry of human peroxisomes on electron micrographs (Q41366899) (← links)
- Polyenoic very-long-chain fatty acids mobilize intracellular calcium from a thapsigargin-insensitive pool in human neutrophils. The relationship between Ca2+ mobilization and superoxide production induced by long- and very-long-chain fatty acids (Q41871987) (← links)
- An apparent decrease in cholesterol biosynthesis in peroxisomal-defective Chinese hamster ovary cells is related to impaired mitochondrial oxidation (Q44454808) (← links)
- Peroxisome mosaicism in the livers of peroxisomal deficiency patients (Q49167581) (← links)
- Peroxisomal localization of the immunoreactive beta-oxidation enzymes in a neonate with a beta-oxidation defect. Pathological observations in liver, adrenal cortex and kidney. (Q54305694) (← links)
- Ultrastructure and immunocytochemistry of hepatic peroxisomes in rhizomelic chondrodysplasia punctata (Q67969615) (← links)
- Morphometry of peroxisomes and immunolocalization of peroxisomal proteins in the liver of patients with generalised peroxisomal disorders (Q71607103) (← links)
- Establishment of a normal range of morphometric values for peroxisomes in paediatric liver (Q72731022) (← links)
- Immunoblot analysis of peroxisomal proteins in liver and fibroblasts from patients (Q73117530) (← links)
- Bile acid treatment alters hepatic disease and bile acid transport in peroxisome-deficient PEX2 Zellweger mice (Q80060299) (← links)
- Initial experience from a renal genetics clinic demonstrates a distinct role in patient management (Q90590108) (← links)
- Peroxisome-Deficiency and HIF-2α Signaling Are Negative Regulators of Ketohexokinase Expression (Q98178400) (← links)