Developmental roles of D-bifunctional protein-A zebrafish model of peroxisome dysfunction. - Wikidata - awgldk - TriplyDB

Developmental roles of D-bifunctional protein-A zebrafish model of peroxisome dysfunction.

Developmental roles of D-bifunctional protein-A zebrafish model of peroxisome dysfunction.

http://www.wikidata.org/entity/Q37532699

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The fatty acid chain elongase, Elovl1, is required for kidney and swim bladder development during zebrafish embryogenesis Metabolic etiologies in West syndrome.

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Developmental roles of D-bifunctional protein-A zebrafish model of peroxisome dysfunction.

http://www.wikidata.org/entity/Q37532699

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 27 January 2014

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Developmental roles of D-bifun ...... del of peroxisome dysfunction.

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Developmental roles of D-bifun ...... del of peroxisome dysfunction.

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type

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Developmental roles of D-bifun ...... del of peroxisome dysfunction.

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Developmental roles of D-bifun ...... del of peroxisome dysfunction.

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prefLabel

Developmental roles of D-bifun ...... del of peroxisome dysfunction.

@en

Developmental roles of D-bifun ...... del of peroxisome dysfunction.

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MOLCELLS.2014.2300

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Molecules and Cells

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Developmental roles of D-bifun ...... del of peroxisome dysfunction.

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Gi-Su Oh

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Hong-Seob So

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Hyung-Jin Kim

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Jong-Young Kwak

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Joon No Lee

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Kyeong-Won Yoo

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Meyoung Cho

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Raekil Park

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Se-Jin Kim

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Seong-Kyu Choe

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P2860

Enoyl-CoA hydratase deficiency: identification of a new type of D-bifunctional protein deficiency

Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency

D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder

Mouse models for peroxisome biogenesis defects and β-oxidation enzyme deficiencies

Stages of embryonic development of the zebrafish

Peroxisomal multifunctional protein-2: the enzyme, the patients and the knockout mouse model

Mitochondrial alterations caused by defective peroxisomal biogenesis in a mouse model for Zellweger syndrome (PEX5 knockout mouse)

Absence of peroxisomes in mouse hepatocytes causes mitochondrial and ER abnormalities

A mouse model for Zellweger syndrome

Molecular basis of d-bifunctional protein deficiency

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74-80

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scholarly article

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10.14348/MOLCELLS.2014.2300

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