Evidence map›Paper›PMID 31228156›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2019

Fluorescent Imaging and Microscopy for Dynamic Processes in Rats.

Ruben M Sandoval, Bruce A Molitoris, Oleg Palygin

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

6 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. New insights into proteinuria/albuminuria.Frontiers in physiology · 2022
    Review
  6. 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

3 authors at 3 institutions in 1 country.

Ruben M SandovalDivision of Nephrology, Indiana University School of Medicine, Indianapolis, IN, USA.
Bruce A MolitorisDivision of Nephrology, Indiana University School of Medicine, Indianapolis, IN, USA.
Oleg PalyginDepartment of Physiology, Medical College of Wisconsin, Milwaukee, WI, USA. opalygin@mcw.edu.
Indianapolis Zoo · USIndiana University – Purdue University Indianapolis · USMedical College of Wisconsin · US

Funding

PROBE DELIVERY COREP30DK079312 · NIDDK · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI DAGHER, PIERRE C · 2007 to 2021
$17.1M
Proximal Tubule Albumin Transport in Disease States.R01DK091623 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI MOLITORIS, BRUCE A · 2011 to 2021
$4.3M
Reducing Nephrotoxicity while enabling read through of missense stop codons by Gentamicin congenersI01BX001137 · VA · RLR VA MEDICAL CENTER · PI BACALLAO, ROBERT L · 2012 to 2020
–
American Heart Association-American Stroke Association 17SDG33660149BLRD VA I01 BX001137NIDDK NIH HHS P30 DK079312NIDDK NIH HHS R01 DK091623
6 · The paper itself

Abstract

The rat is a favored model organism to study physiological function in vivo. This is largely due to the fact that it has been used for decades and is often more comparable to corresponding human conditions (both normal and pathologic) than mice. Although the development of genetic manipulations in rats has been slower than in mice, recent advances of new genomic editing tools allow for the generation of targeted global and specific cell type mutations in different rat strains. The rat is an ideal model for advancing imaging techniques like intravital multi-photon microscopy or IVMPM. Multi-photon excitation microscopy can be applied to visualize real-time physiologic events in multiple organs including the kidney. This imaging modality can generate four-dimensional high resolution images that are inherently confocal due to the fact that the photon density needed to excite fluorescence only occurs at the objective focal plane, not above or below. Additionally, longer excitation wavelengths allow for deeper penetration into tissue, improved excitation, and are inherently less phototoxic than shorter excitation wavelengths. Applying imaging tools to study physiology in rats has become a valuable scientific technique due to the relatively simple surgical procedures, improved quality of reagents, and reproducibility of established assays. In this chapter, the authors provide an example of the application of fluorescent techniques to study cardio-renal functions in rat models. Use of experimental procedures described here, together with multiple available genetically modified animal models, provide new prospective for the further application of multi-photon microscopy in basic and translational research.

Indexed as

AnimalsHeartHumansImaging, Three-DimensionalIntravital MicroscopyKidneyMicroscopy, FluorescenceMicroscopy, Fluorescence, MultiphotonModels, AnimalRatsAlbuminCardio-renalFluorescence microscopyIntravital imagingKidneyMulti-photonRatRat modelsVascular

Identifiers

PMID31228156
PMCPMC6693343
OpenAlexW2952451743

What OpenQuestion holds

Textmetadata
LicenceTDM
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.