(Q33954902)

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Discordant gene expression signatures and related phenotypic differences in lamin A- and A/C-related Hutchinson-Gilford progeria syndrome (HGPS).

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Europe PubMed Central

PubMed publication ID

30 July 2017

Discordant gene expression signatures and related phenotypic differences in lamin A- and A/C-related Hutchinson-Gilford progeria syndrome (HGPS). (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

1 reference

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author name string

Martina Plasilova

1

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Chandon Chattopadhyay

2

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Apurba Ghosh

3

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Friedel Wenzel

4

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Philippe Demougin

5

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Christoph Noppen

6

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Nathalie Schaub

7

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Gabor Szinnai

8

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Luigi Terracciano

9

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Europe PubMed Central

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30 July 2017

Karl Heinimann

10

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Europe PubMed Central

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30 July 2017

language of work or name

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publication date

27 June 2011

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Europe PubMed Central

PubMed publication ID

30 July 2017

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Europe PubMed Central

PubMed publication ID

30 July 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

e21433

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

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Creative Commons Attribution 4.0 International

27 June 2011

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April 2022 Public Data File from Crossref

copyright status

0 references

Cardiovascular pathology in Hutchinson-Gilford progeria: correlation with the vascular pathology of aging.

1 reference

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5 July 2018

Homozygous nonsense mutations in TWIST2 cause Setleis syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Bone and glucose metabolism: a two-way street

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Insulin receptor signaling in osteoblasts regulates postnatal bone acquisition and body composition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Insulin signaling in osteoblasts integrates bone remodeling and energy metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Lower bone mass in prepubertal overweight children with prediabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Defective lamin A-Rb signaling in Hutchinson-Gilford Progeria Syndrome and reversal by farnesyltransferase inhibition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Insulin resistance, adipose depots and gut: interactions and pathological implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Loss-of-function ENPP1 mutations cause both generalized arterial calcification of infancy and autosomal-recessive hypophosphatemic rickets

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Autosomal-recessive hypophosphatemic rickets is associated with an inactivation mutation in the ENPP1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

WNT5A mutations in patients with autosomal dominant Robinow syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

The uncarboxylated form of osteocalcin is associated with improved glucose tolerance and enhanced beta-cell function in middle-aged male subjects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Intermediate filaments: primary determinants of cell architecture and plasticity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Association between serum osteocalcin and markers of metabolic phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Osteoprotegerin, vascular calcification and atherosclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

HGPS and related premature aging disorders: from genomic identification to the first therapeutic approaches

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Reciprocal regulation of bone and energy metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Nuclear lamins: major factors in the structural organization and function of the nucleus and chromatin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Osteocalcin differentially regulates beta cell and adipocyte gene expression and affects the development of metabolic diseases in wild-type mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Phenotype and course of Hutchinson-Gilford progeria syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Endocrine regulation of energy metabolism by the skeleton

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

LEM-Domain proteins: new insights into lamin-interacting proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

"Laminopathies": a wide spectrum of human diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Invertebrate lamins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Ankyrin G overexpression in Hutchinson-Gilford progeria syndrome fibroblasts identified through biological filtering of expression profiles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Farnesylated lamins, progeroid syndromes and farnesyl transferase inhibitors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Lamin A/C expression is a marker of mouse and human embryonic stem cell differentiation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

RACE: Remote Analysis Computation for gene Expression data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Reversal of the cellular phenotype in the premature aging disease Hutchinson-Gilford progeria syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

The nuclear lamina comes of age.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Genome-scale expression profiling of Hutchinson-Gilford progeria syndrome reveals widespread transcriptional misregulation leading to mesodermal/mesenchymal defects and accelerated atherosclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Intermediate filaments: molecular structure, assembly mechanism, and integration into functionally distinct intracellular Scaffolds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Use and abuse of HOMA modeling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

A twist code determines the onset of osteoblast differentiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Idiopathic hyperphosphatasia and TNFRSF11B mutations: relationships between phenotype and genotype.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Genetic regulation of osteoclast development and function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

The receptor tyrosine kinase Ror2 is involved in non-canonical Wnt5a/JNK signalling pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Lamin a truncation in Hutchinson-Gilford progeria.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Lamina-associated polypeptide 2beta (LAP2beta) is contained in a protein complex together with A- and B-type lamins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Membrane glycoprotein PC-1 inhibition of insulin receptor function occurs via direct interaction with the receptor alpha-subunit

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

A Wnt5a pathway underlies outgrowth of multiple structures in the vertebrate embryo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Nuclear lamins: their structure, assembly, and interactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

A- and B-type lamins are differentially expressed in normal human tissues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Osteoprotegerin: a novel secreted protein involved in the regulation of bone density

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Membrane glycoprotein PC-1 and insulin resistance in non-insulin-dependent diabetes mellitus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Cardiovascular abnormalities in progeria. Case report and review of the literature.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Differential timing of nuclear lamin A/C expression in the various organs of the mouse embryo and the young animal: a developmental study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Osteocalcin and matrix Gla protein: vitamin K-dependent proteins in bone

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Insulin release and peripheral sensitivity at the oral glucose tolerance test.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Cells of the cellular immune and hemopoietic system of the mouse lack lamins A/C: distinction versus other somatic cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Severe insulin resistance and diabetes mellitus in mandibuloacral dysplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

5 July 2018

Hutchinson-Gilford progeria syndrome: review of the phenotype.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0021433

21 January 2018

Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0021433

21 January 2018

Homozygous LMNA mutation R527C in atypical Hutchinson-Gilford progeria syndrome: evidence for autosomal recessive inheritance.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0021433

21 January 2018

Twist regulates cytokine gene expression through a negative feedback loop that represses NF-kappaB activity

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0021433

21 January 2018

Osteoprotegerin and osteopontin are expressed at high concentrations within symptomatic carotid atherosclerosis

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0021433

21 January 2018

Linked deficiencies in extracellular PP(i) and osteopontin mediate pathologic calcification associated with defective PC-1 and ANK expression

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0021433

21 January 2018

What is a normal glucose value? Differences in indexes of plasma glucose homeostasis in subjects with normal fasting glucose

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0021433

21 January 2018

Insulin sensitivity indices obtained from oral glucose tolerance testing: comparison with the euglycemic insulin clamp.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0021433

21 January 2018

Osteoprotegerin deficiency and juvenile Paget's disease

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0021433

21 January 2018

Disease progression in Hutchinson-Gilford progeria syndrome: impact on growth and development.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0021433

21 January 2018

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0021433

21 January 2018

Serum osteocalcin level is associated with glucose metabolism and atherosclerosis parameters in type 2 diabetes mellitus

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0021433

21 January 2018

No bones about it: insulin modulates skeletal remodeling

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0021433

21 January 2018

Calretinin as a marker for cardiac myxoma. Diagnostic and histogenetic considerations

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0021433

21 January 2018

Urokinase-type plasminogen activator is a marker of aggressive phenotype and an independent prognostic factor in mismatch repair-proficient colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

29 October 2018

A histone lysine methyltransferase activated by non-canonical Wnt signalling suppresses PPAR-gamma transactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3124505

29 October 2018

Type 1 and type 2 diabetes and incident hip fractures in postmenopausal women

1 reference

https://pubmed.ncbi.nlm.nih.gov/21738662

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progeria: Insulin resistance and hyperglycemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21738662

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recombinant osteoprotegerin for juvenile Paget's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21738662

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prospective study of diabetes and risk of hip fracture: the Nurses' Health Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/21738662

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Histological and ultrastructural features of atherosclerosis in progeria

1 reference

https://pubmed.ncbi.nlm.nih.gov/21738662

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteopenia in insulin-dependent diabetes mellitus; prevalence and aspects of pathophysiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/21738662

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0021433

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

2011PLoSO...621433P

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

ResearchGate publication ID

0 references

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