Correlation between the molecular effects of mutations at the dimer interface of alanine-glyoxylate aminotransferase leading to primary hyperoxaluria type I and the cellular response to vitamin B6.

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Correlation between the molecular effects of mutations at the dimer interface of alanine-glyoxylate aminotransferase leading to primary hyperoxaluria type I and the cellular response to vitamin B6.

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2017 nî lūn-bûn

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2017年学术文章

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Correlation between the molecu ...... llular response to vitamin B6.

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Correlation between the molecu ...... llular response to vitamin B6.

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Correlation between the molecu ...... llular response to vitamin B6.

@en

Correlation between the molecu ...... llular response to vitamin B6.

@nl

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Correlation between the molecu ...... llular response to vitamin B6.

@en

Correlation between the molecu ...... llular response to vitamin B6.

@nl

P1476

Correlation between the molecu ...... ellular response to vitamin B6

@en

P2093

Mirco Dindo

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Rosa Montone

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P2860

Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I

Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1

Crystal structure of alanine:glyoxylate aminotransferase and the relationship between genotype and enzymatic phenotype in primary hyperoxaluria type 1

Human wild-type alanine:glyoxylate aminotransferase and its naturally occurring G82E variant: functional properties and physiological implications

Crystal structure of the S187F variant of human liver alanine: Aminotransferase associated with primary hyperoxaluria type I and its functional implications

Molecular Requirements for Peroxisomal Targeting of Alanine-Glyoxylate Aminotransferase as an Essential Determinant in Primary Hyperoxaluria Type 1

Inference of macromolecular assemblies from crystalline state

Molecular etiology of primary hyperoxaluria type 1: new directions for treatment

A guided tour into subcellular colocalization analysis in light microscopy

Four of the most common mutations in primary hyperoxaluria type 1 unmask the cryptic mitochondrial targeting sequence of alanine:glyoxylate aminotransferase encoded by the polymorphic minor allele.

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s10545-017-0105-8

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263-275

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scholarly article

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10.1007/S10545-017-0105-8

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P433

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P478

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Daniele Dell'Orco

Elisa Oppici

Barbara Cellini

P577

2017-11-06T00:00:00Z

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P698

29110180

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P921

vitamin B6