Evidence map›Paper›PMID 20182354›Full record

ReviewCurrent opinion in hematology2010

Determinants of erythrocyte hydration.

Jesse Rinehart, Erol E Gulcicek, Clinton H Joiner, Richard P Lifton, Patrick G Gallagher

Abstract readReview
In one paragraph

Review in Current opinion in hematology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Disorders of erythrocyte volume homeostasis.International journal of laboratory hematology · 2015
    Review
  5. Article
  6. Article
  7. Article
  8. The Role of Nutrition in Sickle Cell Disease.Nutrition and metabolic insights · 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 at 4 institutions in 1 country.

Jesse RinehartDepartment of Genetics, Yale University School of Medicine, New Haven, CT, USA. patrick.gallagher@yale.edu
Erol E Gulcicek
Clinton H Joiner
Richard P Lifton
Patrick G Gallagher
Cincinnati Children's Hospital Medical Center · USHoward Hughes Medical Institute · USUniversity of Cincinnati Medical Center · USYale University · US

Funding

YALE UNIVERSITY CLINICAL AND TRANSLATIONAL SCIENCE AWARD PROGRAMUL1RR024139 · NCRR · YALE UNIVERSITY · PI SHERWIN, ROBERT S · 2006 to 2011
$56.8M
MOLECULAR BIOLOGY OF HUMAN ERYTHROCYTE ALPHA-SPECTRINR01HL065448 · NHLBI · YALE UNIVERSITY · PI GALLAGHER, PATRICK G · 2000 to 2013
$4.4M
The University of Rochester's Clinical and Translational Science InstituteKL2RR024136 · NCRR · UNIVERSITY OF ROCHESTER · PI PEARSON, THOMAS ARTHUR · 2006 to 2011
$4.3M
Molecular Biology of Erythrocyte AnkyrinR01DK062039 · NIDDK · YALE UNIVERSITY · PI GALLAGHER, PATRICK G · 2002 to 2010
$3.3M
Barrier Insulators in ErythropoiesisR01HL106184 · NHLBI · YALE UNIVERSITY · PI GALLAGHER, PATRICK G · 2011 to 2014
$1.6M
LTQ-Orbitrap Mass Spectrometer for Yale University Keck LaboratoryS10RR024617 · NCRR · YALE UNIVERSITY · PI GULCICEK, EROL E · 2008 to 2008
$500k
NHLBI PROTEOMICS INITIATIVE-N01HV28186N01HV028186 · HV · YALE UNIVERSITY · PI WILLIAMS, KENNETH · 2002 to 2006
–
Howard Hughes Medical InstituteNCRR NIH HHS 1S10RR024617-01NCRR NIH HHS S10 RR024617NCRR NIH HHS UL1 RR024136NCRR NIH HHS UL1 RR024139NHLBI NIH HHS HL65448NHLBI NIH HHS N01 HV028186NHLBI NIH HHS N01-HV-28186NHLBI NIH HHS R01 HL065448NHLBI NIH HHS R01 HL106184NHLBI NIH HHS U54HL07087NIDDK NIH HHS DK62039NIDDK NIH HHS R01 DK062039
6 · The paper itself

Abstract

purpose of reviewMaintenance of cellular water and solute homeostasis is critical for survival of the erythrocyte. Inherited or acquired disorders that perturb this homeostasis jeopardize the erythrocyte, leading to its premature destruction. This study reviews recent progress in our understanding the determinants of erythrocyte hydration and its related disorders. RECENT

findingsThe molecular and genetic bases of primary disorders of erythrocyte hydration are poorly understood. Recent studies have implicated roles for the anion transporter, SLC4A1, and the Rh-associated glycoprotein, RhAG. The most common secondary disorder associated with perturbed hydration of the erythrocyte is sickle cell disease, in which dehydration contributes to disease pathology and clinical complications. Advances in understanding the mechanisms regulating erythrocyte solute and water content, particularly associated with KCl cotransport and Gardos channel activation, have revealed novel signaling mechanisms controlling erythrocyte hydration. These signaling pathways may provide innovative strategies to prevent erythrocyte dehydration in sickle cell disease. SUMMARY: Clinical, translational and biologic studies all contribute to our knowledge of erythrocyte hydration. Understanding the mechanisms controlling erythrocyte water and solute homeostasis will serve as a paradigm for other cells and may reveal new therapeutic targets for disease prevention and treatment.

Indexed as

Anemia, Sickle CellAnimalsBody WaterErythrocytesHomeostasisHumansSignal TransductionWater-Electrolyte Balance

Identifiers

PMID20182354
PMCPMC4155397
OpenAlexW2170131544

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.