Evidence map›Paper›PMID 19283374›Full record

ArticleUrological research2009

Primary cultures of renal proximal tubule cells derived from individuals with primary hyperoxaluria.

Karen L Price, Sally-Anne Hulton, William G van't Hoff, John R Masters, Gill Rumsby

Abstract read
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In one paragraph

Article in Urological research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Karen L PriceInstitute of Urology and Nephrology, University College London, London, UK.
Sally-Anne Hulton
William G van't Hoff
John R Masters
Gill Rumsby

Funding

Effect of hyperoxaluria on gene expression in the kidneyR21DK064002 · NIDDK · UNIVERSITY COLLEGE LONDON · PI RUMSBY, GILL · 2004 to 2005
$216k
NIDDK NIH HHS R21 DK64002
6 · The paper itself

Abstract

The primary hyperoxalurias, PH1 and PH2, are inherited disorders caused by deficiencies of alanine:glyoxylate aminotransferase and glyoxylate reductase, respectively. Mutations in either of these enzymes leads to endogenous oxalate overproduction primarily in the liver, but most pathological effects are exhibited in the kidney ultimately leading to end-stage renal failure and systemic oxalosis. To provide a non-invasive means of accessing kidney cells from individuals with primary hyperoxaluria, we have derived primary cultures of renal proximal tubule cells from the urine of these patients. The cells stain positively for the epithelial markers pan-cytokeratin and zonula occludens 1 and the proximal tubule marker gamma-glutamyl transpeptidase. Mutation analysis confirmed that the cultured cells had the same genotype as the leucocytes of the patients and also expressed glyoxylate reductase at the mRNA level, illustrating their potential value as a source of renal material from these individuals.

Indexed as

AdolescentAlcohol OxidoreductasesBase SequenceCells, CulturedChildChild, PreschoolDNA PrimersEpithelial CellsFemaleGenotypeHumansHyperoxaluria, PrimaryInfantKidney Tubules, ProximalMaleRNA, MessengerAlcohol OxidoreductasesDNA Primersglyoxylate reductaseRNA, Messenger

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.