Evidence map›Paper›PMID 25867084›Full record

ReviewCells2015

Signaling during Kidney Development.

Mirja Krause, Aleksandra Rak-Raszewska, Ilkka Pietilä, Susan E Quaggin, Seppo Vainio

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.0field-weighted citation impact, top 8% of its field
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

35 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Article
  3. The kidney stroma in development and disease.Nature reviews. Nephrology · 2025
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. 3D kidney organoids for bench-to-bedside translation.Journal of molecular medicine (Berlin, Germany) · 2021
    Review
  17. Article
  18. Article
  19. Article
  20. 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 at 3 institutions in 2 countries.

Mirja KrauseFaculty of Biochemistry and Molecular Medicine, Biocenter Oulu, Oulu University, 90014 Oulu, Finland. mirja.krause@oulu.fi.
Aleksandra Rak-RaszewskaFaculty of Biochemistry and Molecular Medicine, Biocenter Oulu, Oulu University, 90014 Oulu, Finland. aleksandra.rak-raszewska@oulu.fi.
Ilkka PietiläFaculty of Biochemistry and Molecular Medicine, Biocenter Oulu, Oulu University, 90014 Oulu, Finland. ilkka.pietila@oulu.fi.
Susan E QuagginNorthwestern University, Feinberg School of Medicine, Chicago, IL 60611, USA. quaggin@northwestern.edu.
Seppo VainioFaculty of Biochemistry and Molecular Medicine, Biocenter Oulu, Oulu University, 90014 Oulu, Finland. seppo.vainio@oulu.fi.
University of Oulu · FINorthwestern University · USOulu University of Applied Sciences · FI

Funding

Exploiting Tie2 Activation for the Treatment of Vascular DiseasesR01HL124120 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI QUAGGIN, SUSAN E. · 2014 to 2017
$1.5M
NHLBI NIH HHS R01 HL124120
6 · The paper itself

Abstract

The kidney plays an essential role during excretion of metabolic waste products, maintenance of key homeostasis components such as ion concentrations and hormone levels. It influences the blood pressure, composition and volume. The kidney tubule system is composed of two distinct cell populations: the nephrons forming the filtering units and the collecting duct system derived from the ureteric bud. Nephrons are composed of glomeruli that filter the blood to the Bowman's capsule and tubular structures that reabsorb and concentrate primary urine. The collecting duct is a Wolffian duct-derived epithelial tube that concentrates and collects urine and transfers it via the renal pelvis into the bladder. The mammalian kidney function depends on the coordinated development of specific cell types within a precise architectural framework. Due to the availability of modern analysis techniques, the kidney has become a model organ defining the paradigm to study organogenesis. As kidney diseases are a problem worldwide, the understanding of mammalian kidney cells is of crucial importance to develop diagnostic tools and novel therapies. This review focuses on how the pattern of renal development is generated, how the inductive signals are regulated and what are their effects on proliferation, differentiation and morphogenesis.

Identifiers

PMID25867084
PMCPMC4493451
OpenAlexW2036504666

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.