Pages that link to "Q24318540"
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The following pages link to Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders (Q24318540):
Displaying 50 items.
- Zellweger syndrome (Q189167) (← links)
- Neonatal adrenoleukodystrophy (Q16965307) (← links)
- Peroxisomal biogenesis factor 10 (Q21125810) (← links)
- MCD encodes peroxisomal and cytoplasmic forms of malonyl-CoA decarboxylase and is mutated in malonyl-CoA decarboxylase deficiency (Q22003808) (← links)
- Peroxisome synthesis in the absence of preexisting peroxisomes (Q22008726) (← links)
- Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly (Q22008838) (← links)
- Identification of peroxisomal acyl-CoA thioesterases in yeast and humans (Q22009090) (← links)
- Characterization of PECI, a novel monofunctional Delta(3), Delta(2)-enoyl-CoA isomerase of mammalian peroxisomes (Q22010424) (← links)
- PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import (Q22010795) (← links)
- PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis (Q22253284) (← links)
- Identification and characterization of HAOX1, HAOX2, and HAOX3, three human peroxisomal 2-hydroxy acid oxidases (Q22253955) (← links)
- Molecular anatomy of the peroxin Pex12p: ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type 1-receptor Pex5p and a ring peroxin, Pex10p (Q22254195) (← links)
- Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients (Q22254302) (← links)
- Identification of PTE2, a human peroxisomal long-chain acyl-CoA thioesterase (Q24289569) (← links)
- Multiple distinct targeting signals in integral peroxisomal membrane proteins (Q24291322) (← links)
- Identification of PEX5p-related novel peroxisome-targeting signal 1 (PTS1)-binding proteins in mammals (Q24291459) (← links)
- Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis (Q24300953) (← links)
- Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders (Q24539414) (← links)
- PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders (Q24540126) (← links)
- The peroxin pex3p initiates membrane assembly in peroxisome biogenesis (Q24549973) (← links)
- Peroxisomes in brain development and function (Q26774697) (← links)
- The peroxin Pex14p. cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysis (Q28142062) (← links)
- Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure (Q28287803) (← links)
- The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum (Q28293113) (← links)
- Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- mice (Q28510846) (← links)
- Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders (Q30168107) (← links)
- Different functions of the C3HC4 zinc RING finger peroxins PEX10, PEX2, and PEX12 in peroxisome formation and matrix protein import (Q30496348) (← links)
- Adrenoleukodystrophy and related disorders (Q30660504) (← links)
- Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders (Q31368357) (← links)
- Peroxisomal remnant structures in Hansenula polymorpha Pex5 cells can develop into normal peroxisomes upon induction of the PTS2 protein amine oxidase. (Q31493205) (← links)
- Peroxisomal disorders: clinical, biochemical, and molecular aspects (Q33607754) (← links)
- Genetic and dietary regulation of lipid droplet expansion in Caenorhabditis elegans (Q33740792) (← links)
- Disorders related to peroxisomal membranes (Q33948568) (← links)
- Peroxisome biogenesis and peroxisome biogenesis disorders (Q33957100) (← links)
- Peroxisome biogenesis disorders: genetics and cell biology (Q33974570) (← links)
- Therapeutic developments in peroxisome biogenesis disorders (Q34075041) (← links)
- How peroxisomes arise. (Q34156679) (← links)
- Peripheral nervous system defects in a mouse model for peroxisomal biogenesis disorders (Q34308359) (← links)
- Genetic and molecular bases of peroxisome biogenesis disorders (Q34362011) (← links)
- AthPEX10, a nuclear gene essential for peroxisome and storage organelle formation during Arabidopsis embryogenesis. (Q35235027) (← links)
- DCA1 Acts as a Transcriptional Co-activator of DST and Contributes to Drought and Salt Tolerance in Rice (Q35818819) (← links)
- Characterization of glycosomal RING finger proteins of trypanosomatids (Q35990056) (← links)
- PEX11 promotes peroxisome division independently of peroxisome metabolism (Q36325799) (← links)
- Inhibitors of COPI and COPII do not block PEX3-mediated peroxisome synthesis (Q36328310) (← links)
- Plant peroxisomes. (Q36402773) (← links)
- Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay (Q36578925) (← links)
- Pex19p interacts with Pex3p and Pex10p and is essential for peroxisome biogenesis in Pichia pastoris (Q36876929) (← links)
- Peroxisome biogenesis and human peroxisome-deficiency disorders (Q37670278) (← links)
- Distinct modes of ubiquitination of peroxisome-targeting signal type 1 (PTS1) receptor Pex5p regulate PTS1 protein import (Q39012365) (← links)
- Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder (Q39638543) (← links)