Evidence map›Paper›PMID 15007650›Full record

ArticlePflugers Archiv : European journal of physiology2004

Segment-specific expression of sodium-phosphate cotransporters NaPi-IIa and -IIc and interacting proteins in mouse renal proximal tubules.

C Madjdpour, D Bacic, B Kaissling, H Murer, J Biber

Abstract read
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In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Structures of the sodium-coupled phosphate importer SLC34A2 reveal a distinct architecture and gating mechanism.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. FGF/FGFR signaling in health and disease.Signal transduction and targeted therapy · 2020
    Review
  4. PF-06869206 is a selective inhibitor of renal PAmerican journal of physiology. Renal physiology · 2020
    Article
  5. Article
  6. Article
  7. Mechanisms of phosphate transport.Nature reviews. Nephrology · 2019
    Review
  8. NaPi-IIa interacting partners and their (un)known functional roles.Pflugers Archiv : European journal of physiology · 2019
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Who regenerates the kidney tubule?Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2015
    Review
  14. Renal phosphate wasting in the absence of adenylyl cyclase 6.Journal of the American Society of Nephrology : JASN · 2014
    Article
  15. Review
  16. Differentiated kidney epithelial cells repair injured proximal tubule.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  17. Proximal nephron.Comprehensive Physiology · 2013
    Review
  18. Article
  19. Fibroblast growth factor 23 regulates renal 1,25-dihydroxyvitamin D and phosphate metabolism via the MAP kinase signaling pathway in Hyp mice.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2011
    Article
  20. Klotho: a novel phosphaturic substance acting as an autocrine enzyme in the renal proximal tubule.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2010
    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.

C MadjdpourInstitute of Anatomy, University of Zurich, 8057, Zurich, Switzerland.
D Bacic
B Kaissling
H Murer
J Biber

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sodium-dependent phosphate cotransport in renal proximal tubules (PTs) is heterogeneous with respect to proximal tubular segmentation (S1 vs. S3) and nephron generation (superficial vs. juxtamedullary). In the present study, S1 and S3 segments of superficial and juxtamedullary nephrons were laser-microdissected and mRNA and protein expression of the Na/Pi-cotransporters NaPi-IIa and NaPi-IIc and the PDZ proteins NHERF-1 and PDZK1 determined. Expression of NaPi-IIa mRNA decreased axially in juxtamedullary nephrons. There was no effect of dietary Pi content on NaPi-lla mRNA expression in any proximal tubular segment. The abundance of the NaPi-IIa cotransporter in the brush-border membrane showed inter- and intranephron heterogeneity and increased in response to a low-Pi diet (5 days), suggesting that up-regulation of NaPi-lla occurs via post-transcriptional mechanisms. In contrast, NaPi-IIc mRNA and protein was up-regulated by the low-Pi diet in all nephron generations analysed. NHERF-1 and PDZK1, at both mRNA and protein levels, were distributed evenly along the PTs and did not change after a low-Pi diet.

Indexed as

AnimalsBlotting, WesternGene ExpressionKidney Tubules, ProximalMaleMembrane ProteinsMiceMice, Inbred StrainsPhosphatesPhosphoproteinsRNA, MessengerSodium-Hydrogen ExchangersSodium-Phosphate Cotransporter ProteinsSodium-Phosphate Cotransporter Proteins, Type IIaSymportersTranscription, GeneticMembrane ProteinsPhosphatesPhosphoproteinsRNA, MessengerSlc34a1 protein, mousesodium-hydrogen exchanger regulatory factorSodium-Hydrogen ExchangersSodium-Phosphate Cotransporter ProteinsSodium-Phosphate Cotransporter Proteins, Type IIaSymporters

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Registered trials

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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.