(Q24337342)

4-hydroxy-2-oxoglutarate aldolase 1

primary hyperoxaluria

1 reference

1 reference

1 reference

oxalate metabolic process

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

Carla G Monico

1

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Sandro Rossetti

2

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Ruth Belostotsky

3

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Andrea G Cogal

4

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Regina M Herges

5

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Barbara M Seide

6

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Julie B Olson

7

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Eric J Bergstrahl

8

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Hugh J Williams

9

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William E Haley

10

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Yaacov Frishberg

11

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Dawn S Milliner

Clinical Journal of the American Society of Nephrology

12

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language of work or name

English

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publication date

September 2011

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published in

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volume

6

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issue

9

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page(s)

2289-95

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cites work

Mutations in DHDPSL are responsible for primary hyperoxaluria type III

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358997

Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358997

Phenotypic and functional analysis of human SLC26A6 variants in patients with familial hyperoxaluria and calcium oxalate nephrolithiasis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358997

Hydroxyproline ingestion and urinary oxalate and glycolate excretion.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358997

Microbial aldolases as C-C bonding enzymes--unknown treasures and new developments

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358997

Importance of mild hyperoxaluria in the pathogenesis of urolithiasis--new evidence from studies in the Arabian peninsula.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358997

Potential mechanisms of marked hyperoxaluria not due to primary hyperoxaluria I or II.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3358997

Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: a novel type of primary hyperoxaluria

29 November 2018

1 reference

12 December 2020

Glyoxylate synthesis, and its modulation and influence on oxalate synthesis

1 reference

12 December 2020

Hyperoxaluria and urolithiasis in young children: an atypical presentation

1 reference

12 December 2020

Kinetic analysis and tissue distribution of human D-glycerate dehydrogenase/glyoxylate reductase and its relevance to the diagnosis of primary hyperoxaluria type 2

1 reference

12 December 2020

The cause of idiopathic calcium stone disease: hypercalciuria or hyperoxaluria?

1 reference

12 December 2020

Hydroxyproline metabolism by the rat kidney: distribution of renal enzymes of hydroxyproline catabolism and renal conversion of hydroxyproline to glycine and serine

1 reference

12 December 2020

Relationship of animal protein-rich diet to kidney stone formation and calcium metabolism

1 reference

12 December 2020