(Q30497302)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20926892%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

title

Induced chromosome deletion in a Williams-Beuren syndrome mouse model causes cardiovascular abnormalities (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20926892%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

1 reference

Williams-Beuren syndrome

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20926892%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

author name string

Hong-Hua Li

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20926892%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Uta Francke

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20926892%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Charles A Taylor

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20926892%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

publication date

7 October 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20926892%20AND%20SRC:MED&resulttype=core&format=json

Journal of Vascular Research

15 February 2020

published in

1 reference

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15 February 2020

volume

48

1 reference

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15 February 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20926892%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

page(s)

119-129

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20926892%20AND%20SRC:MED&resulttype=core&format=json

Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice

15 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Vascular extracellular matrix and arterial mechanics

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Reduced vessel elasticity alters cardiovascular structure and function in newborn mice.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Elastin haploinsufficiency induces alternative aging processes in the aorta.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Hemizygosity at the NCF1 gene in patients with Williams-Beuren syndrome decreases their risk of hypertension.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Developmental adaptation of the mouse cardiovascular system to elastin haploinsufficiency

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Mutational mechanisms of Williams-Beuren syndrome deletions

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Connection between elastin haploinsufficiency and increased cell proliferation in patients with supravalvular aortic stenosis and Williams-Beuren syndrome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Fibulin-5/DANCE is essential for elastogenesis in vivo

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Mouse models of genetic diseases resulting from mutations in elastic fiber proteins

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

I. The neurocognitive profile of Williams Syndrome: a complex pattern of strengths and weaknesses

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Novel arterial pathology in mice and humans hemizygous for elastin

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Elastin is an essential determinant of arterial morphogenesis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Elastin: genomic structure and point mutations in patients with supravalvular aortic stenosis.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

A Lamellar Unit of Aortic Medial Structure and Function in Mammals

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Non-invasive assessment of the age related changes in stiffness of major branches of the human arteries.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Diameter and compliance in the male human abdominal aorta: influence of age and aortic aneurysm.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Increased anterior abdominal aortic wall motion: possible role in aneurysm pathogenesis and design of endovascular devices.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Vascular Wall Remodeling in Patients with Supravalvular Aortic Stenosis and Williams Beuren Syndrome

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Genomic organization of the genes Gtf2ird1, Gtf2i, and Ncf1 at the mouse chromosome 5 region syntenic to the human chromosome 7q11.23 Williams syndrome critical region.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Pathology of coronary arteries, myocardium, and great arteries in supravalvular aortic stenosis. Report of five cases with implications for surgical treatment.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

The cholinergic innervation of the aorta

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975735

Partial off-loading of longitudinal tension induces arterial tortuosity

26 November 2018

1 reference

12 December 2020

Effects of elastin haploinsufficiency on the mechanical behavior of mouse arteries

1 reference

12 December 2020

Overview of extracellular matrix

1 reference

12 December 2020

Vascular reactivity of isolated thoracic aorta of the C57BL/6J mouse

1 reference

12 December 2020

Exercise testing and 24-hour ambulatory blood pressure monitoring in children with Williams syndrome

1 reference

12 December 2020

"Everybody in the world is my friend" hypersociability in young children with Williams syndrome

1 reference

12 December 2020

Systemic hypertension secondary to peripheral vascular anomalies in patients with Williams syndrome

1 reference

12 December 2020

Supravalvular aortic stenosis. Clinical and pathologic observations in six patients

1 reference

12 December 2020

Generalized arteriopathy in williams syndrome: An intravascular ultrasound study

1 reference

12 December 2020

Elastic lamina growth in the developing mouse aorta

1 reference

12 December 2020

Mid-aortic syndrome presenting in childhood

1 reference

12 December 2020

The middle aortic syndrome: an important feature of Williams' syndrome

1 reference

12 December 2020

Pathology of the diffuse variant of supravalvar aortic stenosis

1 reference

12 December 2020

Identifiers

DOI

10.1159/000316808

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20926892%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20926892%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

PubMed publication ID

20926892

1 reference