(Q26781983)

2

0 references

author name string

Jeffrey Baron

1

0 references

Francesco De Luca

3

0 references

Andrew Dauber

4

0 references

Moshe Phillip

5

0 references

Jan M Wit

Nature Reviews Endocrinology

6

0 references

language of work or name

English

0 references

publication date

December 2015

0 references

published in

0 references

volume

11

0 references

issue

12

0 references

page(s)

735-46

0 references

cites work

The 3M complex maintains microtubule and genome integrity

1 reference

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Identification and functional characterization of two novel NPR2 mutations in Japanese patients with short stature

7 April 2017

1 reference

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Heterozygous mutations in natriuretic peptide receptor-B (NPR2) gene as a cause of short stature in patients initially classified as idiopathic short stature

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Mutations in the pre-replication complex cause Meier-Gorlin syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Hundreds of variants clustered in genomic loci and biological pathways affect human height

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Mutations in the transmembrane natriuretic peptide receptor NPR-B impair skeletal growth and cause acromesomelic dysplasia, type Maroteaux

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Recent research on the growth plate: Impact of inflammatory cytokines on longitudinal bone growth

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Recent research on the growth plate: Advances in fibroblast growth factor signaling in growth plate development and disorders

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Delayed puberty and estrogen resistance in a woman with estrogen receptor α variant

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Sixteen years and counting: the current understanding of fibroblast growth factor receptor 3 (FGFR3) signaling in skeletal dysplasias

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Angiotensin II blockade and aortic-root dilation in Marfan's syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Mutations in the pericentrin (PCNT) gene cause primordial dwarfism

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

FGF18 is required for early chondrocyte proliferation, hypertrophy and vascular invasion of the growth plate

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Targeted disruption of the biglycan gene leads to an osteoporosis-like phenotype in mice

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Estrogen resistance caused by a mutation in the estrogen-receptor gene in a man

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Thyroid hormone interacts with the Wnt/beta-catenin signaling pathway in the terminal differentiation of growth plate chondrocytes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

FGF9 regulates early hypertrophic chondrocyte differentiation and skeletal vascularization in the developing stylopod

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Interleukin-1beta and TNF-alpha act in synergy to inhibit longitudinal growth in fetal rat metatarsal bones

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Expression of estrogen receptors and enzymes involved in sex steroid metabolism in the rat tibia during sexual maturation

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Dwarfism and early death in mice lacking C-type natriuretic peptide

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Fibroblast growth factor expression in the postnatal growth plate

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans

7 April 2017

1 reference

https://api.crossref.org/works/10.1038/NRENDO.2015.165

A type X collagen mutation causes Schmid metaphyseal chondrodysplasia

22 April 2017

1 reference

https://api.crossref.org/works/10.1038/NRENDO.2015.165

Some chondrodysplasias with short limbs: molecular perspectives

22 April 2017

1 reference

https://api.crossref.org/works/10.1038/NRENDO.2015.165

Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation

22 April 2017

1 reference

https://api.crossref.org/works/10.1038/NRENDO.2015.165

Developmental regulation of the growth plate

22 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Dysregulation of TGF-beta activation contributes to pathogenesis in Marfan syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Heterozygous mutations in natriuretic peptide receptor-B (NPR2) gene as a cause of short stature

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Defining the role of common variation in the genomic and biological architecture of adult human height

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

"RAF" neighborhood: protein-protein interaction in the Raf/Mek/Erk pathway

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Genetic evaluation of short stature.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Short stature, accelerated bone maturation, and early growth cessation due to heterozygous aggrecan mutations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Recent research on the growth plate: Recent insights into the regulation of the growth plate

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Reprint of: Heparan sulfate as a regulator of endochondral ossification and osteochondroma development

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Evidence that estrogen hastens epiphyseal fusion and cessation of longitudinal bone growth by irreversibly depleting the number of resting zone progenitor cells in female rabbits

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Copy number variants in patients with short stature.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Large-scale pooled next-generation sequencing of 1077 genes to identify genetic causes of short stature

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Low incidence of pathology detection and high cost of screening in the evaluation of asymptomatic short children

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Rare copy number variants are a common cause of short stature

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Safe, accurate, prenatal diagnosis of thanatophoric dysplasia using ultrasound and free fetal DNA.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Glucocorticoids and the regulation of growth hormone secretion

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Evaluation of the therapeutic potential of a CNP analog in a Fgfr3 mouse model recapitulating achondroplasia

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Fibrillin-1 mutations causing Weill-Marchesani syndrome and acromicric and geleophysic dysplasias disrupt heparan sulfate interactions

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

The effect of acute and chronic stress on growth

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Synthesizing genome-wide association studies and expression microarray reveals novel genes that act in the human growth plate to modulate height

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Mutations in EZH2 cause Weaver syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Aromatase inhibitors in pediatrics

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Mechanisms and pathways of growth failure in primordial dwarfism.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Unraveling the transcriptional regulatory machinery in chondrogenesis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

The musculoskeletal phenotype of the RASopathies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Short stature due to SHOX deficiency: genotype, phenotype, and therapy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

New aids for the non-invasive prenatal diagnosis of achondroplasia: dysmorphic features, charts of fetal size and molecular confirmation using cell-free fetal DNA in maternal plasma.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Deletion and point mutations of PTHLH cause brachydactyly type E.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

A missense mutation in the aggrecan C-type lectin domain disrupts extracellular matrix interactions and causes dominant familial osteochondritis dissecans

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Idiopathic short stature: conundrums of definition and treatment

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Effect of body mass index on peak growth hormone response to provocative testing in children with short stature

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Overgrowth syndromes:from classical to new.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Update on the role of aromatase inhibitors in growth disorders

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

A recessive skeletal dysplasia, SEMD aggrecan type, results from a missense mutation affecting the C-type lectin domain of aggrecan

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Nitric oxide, C-type natriuretic peptide and cGMP as regulators of endochondral ossification.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Idiopathic short stature: definition, epidemiology, and diagnostic evaluation.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

C-natriuretic peptide: an important regulator of cartilage.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Wnt gene expression in the post-natal growth plate: regulation with chondrocyte differentiation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

BMP signaling in the cartilage growth plate.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Is there a role for recombinant insulin-like growth factor-I in the treatment of idiopathic short stature?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

The restricted potential for recovery of growth plate chondrogenesis and longitudinal bone growth following exposure to pro-inflammatory cytokines.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Locally produced estrogen promotes fetal rat metatarsal bone growth; an effect mediated through increased chondrocyte proliferation and decreased apoptosis.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Interaction of fibroblast growth factor and C-natriuretic peptide signaling in regulation of chondrocyte proliferation and extracellular matrix homeostasis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Endocrine regulation of the growth plate

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Identification of mutations in CUL7 in 3-M syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

The molecular basis of idiopathic short stature

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Effect of growth hormone treatment on adult height in peripubertal children with idiopathic short stature: a randomized, double-blind, placebo-controlled trial

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Chondrodysplasia of gene knockout mice for aggrecan and link protein

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Growth without growth hormone.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Effects of estrogen on growth plate senescence and epiphyseal fusion

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Regulation of growth plate chondrogenesis by bone morphogenetic protein-2.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Growth hormone axis overview--somatomedin hypothesis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Gly369Cys mutation in mouse FGFR3 causes achondroplasia by affecting both chondrogenesis and osteogenesis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Differential effects of insulin-like growth factor I and growth hormone on developmental stages of rat growth plate chondrocytes in vivo

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Estimation of somatomedin-C levels in normals and patients with pituitary disease by radioimmunoassay

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

A novel homozygous mutation in FGFR3 causes tall stature, severe lateral tibial deviation, scoliosis, hearing impairment, camptodactyly, and arachnodactyly

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Stimulatory effects of insulin-like growth factor-I on growth plate chondrogenesis are mediated by nuclear factor-kappaB p65

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Endochondral growth in growth plates of three species at two anatomical locations modulated by mechanical compression and tension

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

A mutation in the variable repeat region of the aggrecan gene (AGC1) causes a form of spondyloepiphyseal dysplasia associated with severe, premature osteoarthritis

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Evidence supporting dual, IGF-I-independent and IGF-I-dependent, roles for GH in promoting longitudinal bone growth.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Does repetitive physical loading inhibit radial growth in female gymnasts?

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Direct administration of testosterone increases rat tibial epiphyseal growth plate width.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

TSH secretion in Cushing's syndrome: relation to glucocorticoid excess, diabetes, goitre, and the 'sick euthyroid syndrome'.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Dexamethasone acts locally to inhibit longitudinal bone growth in rabbits

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Short stature and growth hormone deficiency

31 May 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

The continuum of growth hormone-IGF-I axis defects causing short stature: diagnostic and therapeutic challenges

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

THE INFLUENCE OF BLOOD GLUCOSE ON THE PLASMA CONCENTRATION OF GROWTH HORMONE.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Relationship between serum growth hormone binding protein levels and height in young men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

The Advantage of Measuring Stimulated as Compared with Spontaneous Growth Hormone Levels in the Diagnosis of Growth Hormone Deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Children with idiopathic short stature are poor eaters and have decreased body mass index.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Heterozygous mutations in natriuretic peptide receptor-B (NPR2) are associated with short stature.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Insulin-like growth factor-I augments chondrocyte hypertrophy and reverses glucocorticoid-mediated growth retardation in fetal mice metatarsal cultures.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Thyroid hormones regulate fibroblast growth factor receptor signaling during chondrogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Sexual dimorphism of growth plate prehypertrophic and hypertrophic chondrocytes in response to testosterone requires metabolism to dihydrotestosterone (DHT) by steroid 5-alpha reductase type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

The role of estrogen receptor α in growth plate cartilage for longitudinal bone growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Final height and gonad function after total body irradiation during childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Guided growth for the treatment of limb length discrepancy: a comparative study of the three most commonly used surgical techniques

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Gradients in bone morphogenetic protein-related gene expression across the growth plate.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Regulation of cell polarity in the cartilage growth plate and perichondrium of metacarpal elements by HOXD13 and WNT5A

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

A novel variant of FGFR3 causes proportionate short stature

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

FGF signaling inhibits chondrocyte proliferation and regulates bone development through the STAT-1 pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Induction of growth plate cartilage ossification by basic fibroblast growth factor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Interaction of FGF, Ihh/Pthlh, and BMP signaling integrates chondrocyte proliferation and hypertrophic differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Regulation of fetal rat bone growth by C-type natriuretic peptide and cGMP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

An activating mutation in the kinase homology domain of the natriuretic peptide receptor-2 causes extremely tall stature without skeletal deformities

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Overgrowth syndrome associated with a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Systemic administration of C-type natriuretic peptide as a novel therapeutic strategy for skeletal dysplasias

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Ext1-dependent heparan sulfate regulates the range of Ihh signaling during endochondral ossification

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Aggrecan is required for growth plate cytoarchitecture and differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

The sitting height/height ratio for age in healthy and short individuals and its potential role in selecting short children for SHOX analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Increased number of sex chromosomes affects height in a nonlinear fashion: a study of 305 patients with sex chromosome aneuploidy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Spectrum of mutations in Noonan syndrome and their correlation with phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Growth hormone and insulin-like growth factor I insensitivity of fibroblasts isolated from a patient with an I{kappa}B{alpha} mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Common DNA variants predict tall stature in Europeans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Optimizing growth hormone therapy in growth hormone deficient children: what to do in the absence of hard evidence? Commentary on Rachmiel et al.: Final height in children with idiopathic growth hormone deficiency treated with a fixed dose of recomb

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

PAPSS2 mutations cause autosomal recessive brachyolmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

PAPSS2 deficiency causes androgen excess via impaired DHEA sulfation--in vitro and in vivo studies in a family harboring two novel PAPSS2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Growth hormone is effective in treatment of short stature associated with short stature homeobox-containing gene deficiency: Two-year results of a randomized, controlled, multicenter trial.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Dose-dependent effect of growth hormone on final height in children with short stature without growth hormone deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Growth plate senescence is associated with loss of DNA methylation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Distinct, autosomal recessive form of spondyloepimetaphyseal dysplasia segregating in an inbred Pakistani kindred

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Effects of fibroblast growth factor-2 on longitudinal bone growth

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

The effects of estrogen priming and puberty on the growth hormone response to standardized treadmill exercise and arginine-insulin in normal girls and boys.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5002943

Regular fluctuations in growth hormone (GH) release determine normal human growth

28 November 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Prednisone dose limitation of growth hormone treatment of steroid-induced growth failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Pro-Inflammatory Cytokines Produced by Growth Plate Chondrocytes May Act Locally to Modulate Longitudinal Bone Growth

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Enlargement of growth plate chondrocytes modulated by sustained mechanical loading

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Overexpression of CNP in chondrocytes rescues achondroplasia through a MAPK-dependent pathway

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

A cluster of translocation breakpoints in 2q37 is associated with overexpression of NPPC in patients with a similar overgrowth phenotype

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Cyclic GMP-dependent protein kinase II plays a critical role in C-type natriuretic peptide-mediated endochondral ossification

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

Rare hereditary diseases with defects in DNA-repair

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2015.165

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NRENDO.2015.165

1 reference

Dimensions Publication ID

1042440971

0 references

1 reference

1 reference

PubMed publication ID

26437621

1 reference