Evidence map›Paper›PMID 19953292›Full record

ReviewCellular and molecular life sciences : CMLS2010

The Rh protein family: gene evolution, membrane biology, and disease association.

Cheng-Han Huang, Mao Ye

Open access · greenAbstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Fasting in the ureotelic Lake Magadi tilapia,Conservation physiology · 2019
    Article
  9. Article
  10. Article
  11. Mechanisms of ammonia and ammonium transport by rhesus-associated glycoproteins.American journal of physiology. Cell physiology · 2015
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Molecular genetics and clinical applications for RH.Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis · 2011
    Review
  19. Article
  20. Review
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

2 authors at 1 institution in 1 country.

Cheng-Han HuangLaboratory of Biochemistry and Molecular Genetics, Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA. chuang@nybloodcenter.org
Mao Ye
New York Blood Center · US

Funding

STUDIES ON THE DUFFY BLOOD GROUP (FY) ANTIGENP50HL054459 · NHLBI · NEW YORK BLOOD CENTER · PI HALVERSON, GREGORY RAY · 1996 to 2005
$8.6M
RH PROTEIN AND THE RH BLOOD GROUP SYSTEMR01HL066274 · NHLBI · NEW YORK BLOOD CENTER · PI HUANG, CHEN-HAN · 2001 to 2004
$1.4M
NHLBI NIH HHS HL54459NHLBI NIH HHS HL66274NHLBI NIH HHS P50 HL054459NHLBI NIH HHS R01 HL066274NICHD NIH HHS HD62704
6 · The paper itself

Abstract

The Rh (Rhesus) genes encode a family of conserved proteins that share a structural fold of 12 transmembrane helices with members of the major facilitator superfamily. Interest in this family has arisen from the discovery of Rh factor's involvement in hemolytic disease in the fetus and newborn, and of its homologs widely expressed in epithelial tissues. The Rh factor and Rh-associated glycoprotein (RhAG), with epithelial cousins RhBG and RhCG, form four subgroups conferring upon vertebrates a genealogical commonality. The past decade has heralded significant advances in understanding the phylogenetics, allelic diversity, crystal structure, and biological function of Rh proteins. This review describes recent progress on this family and the molecular insights gleaned from its gene evolution, membrane biology, and disease association. The focus is on its long evolutionary history and surprising structural conservation from prokaryotes to humans, pointing to the importance of its functional role, related to but distinct from ammonium transport proteins.

Indexed as

AnimalsBlood Group IncompatibilityCell MembraneEvolution, MolecularHumansMultigene FamilyRh-Hr Blood-Group SystemRh-Hr Blood-Group System

Identifiers

PMID19953292
PMCPMC11115862
OpenAlexW2014257720

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.