(Q50512705)

14 March 2018

title

Rapid isolation and characterization of CHO mutants deficient in peroxisome biogenesis using the peroxisomal forms of fluorescent proteins. (English)

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14 March 2018

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M Ito

1

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14 March 2018

R Ito

2

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14 March 2018

Y Huang

3

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14 March 2018

S Miura

4

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A Imamura

5

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14 March 2018

Y Suzuki

6

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N Shimozawa

7

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publication date

1 April 2000

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14 March 2018

Biochimica et Biophysica Acta

published in

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14 March 2018

volume

1496

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14 March 2018

issue

2-3

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14 March 2018

page(s)

232-242

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14 March 2018

describes a project that uses

SK24

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SK32

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cites work

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups

1 reference

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7 January 2021

Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts

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7 January 2021

Isolation of animal cell mutants deficient in plasmalogen biosynthesis and peroxisome assembly

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7 January 2021

Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes

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7 January 2021

Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant

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7 January 2021

A human gene responsible for Zellweger syndrome that affects peroxisome assembly

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7 January 2021

Green fluorescent protein as a marker for gene expression

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7 January 2021

Identification of a peroxisomal targeting signal at the carboxy terminus of firefly luciferase

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4889%2800%2900019-7

7 January 2021

Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting.

1 reference

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7 January 2021

Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein

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7 January 2021

A rapid selection for animal cell mutants with defective peroxisomes.

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Proliferative activation of quiescent Rat-1A cells by delta FosB.

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7 January 2021

Metastatic phenotype in hybrid cells derived from B16 melanoma

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7 January 2021

Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome

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7 January 2021

Isolation of a new peroxisome-deficient CHO cell mutant defective in peroxisome targeting signal-1 receptor

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7 January 2021

Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders

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7 January 2021

Molecular defects in genetic diseases of peroxisomes

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7 January 2021

PAS7 encodes a novel yeast member of the WD-40 protein family essential for import of 3-oxoacyl-CoA thiolase, a PTS2-containing protein, into peroxisomes

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7 January 2021

PEB1 (PAS7) in Saccharomyces cerevisiae encodes a hydrophilic, intra-peroxisomal protein that is a member of the WD repeat family and is essential for the import of thiolase into peroxisomes

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7 January 2021

Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants

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7 January 2021

An isoform of pex5p, the human PTS1 receptor, is required for the import of PTS2 proteins into peroxisomes

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7 January 2021

Pex18p and Pex21p, a novel pair of related peroxins essential for peroxisomal targeting by the PTS2 pathway

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7 January 2021

10.1016/S0167-4889(00)00019-7

Identifiers

DOI

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14 March 2018

PubMed ID

10771091

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14 March 2018