Recurrent exercise-induced acute kidney injury by idiopathic renal hypouricemia with a novel mutation in the SLC2A9 gene and literature review (Q35120577)

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English	Recurrent exercise-induced acute kidney injury by idiopathic renal hypouricemia with a novel mutation in the SLC2A9 gene and literature review	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

4 references

29 May 2020

1 September 2020

6 November 2020

28 November 2023

1 reference

PubMed publication ID

Recurrent exercise-induced acute kidney injury by idiopathic renal hypouricemia with a novel mutation in the SLC2A9 gene and literature review (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

acute kidney injury

3 references

29 May 2020

1 September 2020

6 November 2020

renal tubular transport disease

3 references

15 December 2019

1 September 2020

6 November 2020

urinary calculi

1 reference

14 September 2019

2 references

14 September 2019

6 November 2020

glucose transporters

1 reference

28 November 2019

physical exercise

2 references

PubMed publication ID

1 September 2020

author name string

Huijun Shen

1

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Chunyue Feng

2

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Xia Jin

3

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Jianhua Mao

4

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Haidong Fu

5

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Weizhong Gu

6

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Ai'min Liu

7

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Qiang Shu

8

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Lizhong Du

9

1 reference

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PubMed publication ID

6 August 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

14 March 2014

11 references

Europe PubMed Central

PubMed publication ID

6 August 2017

13 March 2019

22 April 2019

20 June 2019

30 June 2019

14 September 2019

28 November 2019

15 December 2019

1 September 2020

6 November 2020

28 November 2023

12 references

Europe PubMed Central

PubMed publication ID

6 August 2017

13 March 2019

22 April 2019

20 June 2019

30 June 2019

14 September 2019

28 November 2019

15 December 2019

29 May 2020

1 September 2020

6 November 2020

28 November 2023

14

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

73

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

copyright license

Creative Commons Attribution 2.0 Generic

10 references

Europe PubMed Central

13 March 2019

Europe PubMed Central

22 April 2019

Europe PubMed Central

20 June 2019

Europe PubMed Central

30 June 2019

Europe PubMed Central

14 September 2019

Europe PubMed Central

28 November 2019

Europe PubMed Central

15 December 2019

Europe PubMed Central

1 September 2020

Europe PubMed Central

6 November 2020

Europe PubMed Central

28 November 2023

copyright status

0 references

on focus list of Wikimedia project

0 references

Recurrent exercise-induced acute renal failure in a young Pakistani man with severe renal hypouricemia and SLC2A9 compound heterozygosity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

9 July 2018

Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

9 July 2018

A case of exercise-induced acute renal failure with G774A mutation in SCL22A12 causing renal hypouricemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

9 July 2018

Homozygous SLC2A9 mutations cause severe renal hypouricemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

9 July 2018

Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

9 July 2018

SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

9 July 2018

Identification and characterization of human glucose transporter-like protein-9 (GLUT9): alternative splicing alters trafficking.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

9 July 2018

Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

9 July 2018

Molecular identification of a renal urate anion exchanger that regulates blood urate levels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

9 July 2018

Cloning and expression analysis of a novel member of the facilitative glucose transporter family, SLC2A9 (GLUT9)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

9 July 2018

Reference ranges for plasma cystatin C and creatinine measurements in premature infants, neonates, and older children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

9 July 2018

Renal hypouricemia: prevention of exercise-induced acute renal failure and a review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

9 July 2018

Acute renal failure due to uric acid nephropathy in a patient with renal hypouricemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

9 July 2018

Acute kidney injury in two children caused by renal hypouricaemia type 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

27 September 2018

A case of acute renal failure after exercise with renal hypouricemia demonstrated compound heterozygous mutations of uric acid transporter 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

27 September 2018

Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: biochemical and molecular genetic analysis in two Czech families with xanthinuria type I.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

27 September 2018

Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

27 September 2018

Two cases of nephrotic syndrome (NS)-induced acute kidney injury (AKI) associated with renal hypouricemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

27 September 2018

Recurrent EIARF and PRES with severe renal hypouricemia by compound heterozygous SLC2A9 mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

27 September 2018

Plasma urate level is directly regulated by a voltage-driven urate efflux transporter URATv1 (SLC2A9) in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

27 September 2018

Two male siblings with hereditary renal hypouricemia and exercise-induced ARF.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3984694

27 September 2018

The use of plasma creatinine concentration for estimating glomerular filtration rate in infants, children, and adolescents

1 reference

https://pubmed.ncbi.nlm.nih.gov/24628802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patients with renal hypouricemia are prone to develop acute renal failure--why?

1 reference

https://pubmed.ncbi.nlm.nih.gov/24628802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Xanthinuria type I: a rare cause of urolithiasis

1 reference

https://pubmed.ncbi.nlm.nih.gov/24628802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel homozygous insertion in SLC2A9 gene caused renal hypouricemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/24628802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic tests for primary renal hypouricemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/24628802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary renal hypouricemia: a new role for allopurinol?

1 reference

https://pubmed.ncbi.nlm.nih.gov/24628802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2431-14-73

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

ResearchGate publication ID

0 references

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