Molecular and neurologic findings of peroxisome biogenesis disorders.

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Yeast peroxisomes multiply by growth and division.A Drosophila model for the Zellweger spectrum of peroxisome biogenesis disorders.Novel PEX3 Gene Mutations Resulting in a Moderate Zellweger Spectrum Disorder.

P2860

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P2860

Molecular and neurologic findings of peroxisome biogenesis disorders.

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http://www.wikidata.org/entity/Q36142065

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2005 nî lūn-bûn

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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2005年论文

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2005年论文

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name

Molecular and neurologic findings of peroxisome biogenesis disorders.

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Molecular and neurologic findings of peroxisome biogenesis disorders.

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type

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Molecular and neurologic findings of peroxisome biogenesis disorders.

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Molecular and neurologic findings of peroxisome biogenesis disorders.

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prefLabel

Molecular and neurologic findings of peroxisome biogenesis disorders.

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Molecular and neurologic findings of peroxisome biogenesis disorders.

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P1476

Molecular and neurologic findings of peroxisome biogenesis disorders.

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P2093

Michinori Funato

http://www.w3.org/2001/XMLSchema#string

Naomi Kondo

http://www.w3.org/2001/XMLSchema#string

Nobuyuki Shimozawa

http://www.w3.org/2001/XMLSchema#string

Tomoko Nagase

http://www.w3.org/2001/XMLSchema#string

Yasuhiko Takemoto

http://www.w3.org/2001/XMLSchema#string

Yasuyuki Suzuki

http://www.w3.org/2001/XMLSchema#string

P2860

Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene

A human gene responsible for Zellweger syndrome that affects peroxisome assembly

Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders

Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders

Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders

Peroxisomal localization in the developing mouse cerebellum: implications for neuronal abnormalities related to deficiencies in peroxisomes

Abnormal cerebellar histogenesis in PEX2 Zellweger mice reflects multiple neuronal defects induced by peroxisome deficiency

Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients.

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.

P304

326-329

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scholarly article

P356

10.1177/08830738050200041001

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P478

http://www.w3.org/2001/XMLSchema#string

P577

2005-04-01T00:00:00Z

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P698

15921234

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Molecular and neurologic findings of peroxisome biogenesis disorders.

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P2860

P2860

Molecular and neurologic findings of peroxisome biogenesis disorders.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698