Evidence map›Paper›PMID 10905371›Full record

ReviewEndocrine2000

Physiology and disorders of the growth hormone receptor (GHR) and GH-GHR signal transduction.

A L Rosenbloom

Abstract readReview
PubMed Publisher
In one paragraph

Review in Endocrine, 2000. 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
1.0field-weighted citation impact, top 24% 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, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Growth Hormone Receptor Mutations Related to Individual Dwarfism.International journal of molecular sciences · 2018
    Review
  5. Review
  6. Nanomedicines in the treatment of acromegaly: focus on pegvisomant.International journal of nanomedicine · 2006
    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

1 author at 1 institution in 1 country.

A L RosenbloomDepartment of Pediatrics, University of Florida College of Medicine, Gainesville, USA.
Florida College · US

Funding

BODY COMPOSITION IN IGF-I TREATED GH-RECEPTOR DEFICIENCYR01DK045830 · NIDDK · UNIVERSITY OF FLORIDA · PI ROSENBLOOM, ARLAN L. · 1993 to 1996
–
NIDDK NIH HHS DK-45830
6 · The paper itself

Abstract

GH exerts its actions through binding with two receptor molecules at the cell surface and interaction with Janus kinase and signal transducers and activators of transcription, and other likely effectors to stimulate metabolic effects and IGF synthesis. The circulating GH binding protein is the proteolytic product of the cell surface receptor and serves as a marker of receptor number and function. Thirty-six distinct mutations of the receptor in the extracellular and transmembrane domains cause a clinical picture of severe GH/IGF-I deficiency, whereas two dominant negative mutations of the intracellular domain result in a milder clinical syndrome. These mutations have provided insight into the physiology of the GH receptor. A few patients have been described with what appears to be primary GH insensitivity due to defective signal transduction by the GH-GH-receptor complex. Clinical and biochemical features of primary GH insensitivity are not a function of genotype, with as much variability in a genetically homogeneous population as in a heterogeneous one. Except for those dominant negative mutations where co-transfection of the mutant GH receptor gene with wild-type receptor gene has been informative, evidence for an effect of a single mutant allele remains speculative. Treatment of GH receptor deficiency with recombinant human IGF-I suggests that the absence of a direct effect of GH limits growth response.

Indexed as

AnimalsChildCraniofacial AbnormalitiesGrowth DisordersGrowth HormoneHuman Growth HormoneHumansInsulin-Like Growth Factor IReceptors, SomatotropinSignal TransductionGrowth HormoneHuman Growth HormoneInsulin-Like Growth Factor IReceptors, Somatotropin

Identifiers

PMID10905371
OpenAlexW2054051380

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.