MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin II (Q34000032)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17666408%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

title

MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin II (English)

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2 January 2020

0 references

1 reference

10

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2 January 2020

C. S. Raman

13

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2 January 2020

L. Maximilian Buja

14

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2 January 2020

author name string

Hariyadarshi Pannu

1

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2 January 2020

Van Tran-Fadulu

2

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Christina L Papke

3

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Steve Scherer

4

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Yaozhong Liu

5

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Caroline Presley

6

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Dongchuan Guo

7

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2 January 2020

Anthony L Estrera

8

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2 January 2020

Hazim J Safi

9

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G Wesley Vick

11

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A J Marian

12

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Dianna M Milewicz

15

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publication date

31 July 2007

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2 January 2020

published in

Human Molecular Genetics

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2 January 2020

volume

16

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2 January 2020

issue

20

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2 January 2020

page(s)

2453-2462

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Angiotensin II induces IL-6 expression and the Jak-STAT3 pathway in aortic adventitia of LDL receptor-deficient mice

2 January 2020

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Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus

5 July 2018

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A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

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Mapping a locus for familial thoracic aortic aneurysms and dissections (TAAD2) to 3p24-25.

5 July 2018

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Global expression profiling of fibroblast responses to transforming growth factor-beta1 reveals the induction of inhibitor of differentiation-1 and provides evidence of smooth muscle cell phenotypic switching

5 July 2018

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Mutation of the myosin converter domain alters cross-bridge elasticity

5 July 2018

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Identification of a chromosome 11q23.2-q24 locus for familial aortic aneurysm disease, a genetically heterogeneous disorder

5 July 2018

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The molecular genetic basis for hypertrophic cardiomyopathy

5 July 2018

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Angiotensin II blockade reverses myocardial fibrosis in a transgenic mouse model of human hypertrophic cardiomyopathy

5 July 2018

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Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9

5 July 2018

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The way things move: looking under the hood of molecular motor proteins

5 July 2018

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Familial patterns of thoracic aortic aneurysms.

5 July 2018

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Diagnosis and treatment of diseases of the aorta

5 July 2018

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Three-dimensional structure of myosin subfragment-1: a molecular motor

5 July 2018

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Satisfying hydrogen bonding potential in proteins

5 July 2018

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5 July 2018

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A point mutation in the SH1 helix alters elasticity and thermal stability of myosin II.

5 July 2018

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Evidence that insulin-like growth factor-1 requires protein kinase C-epsilon, PI3-kinase and mitogen-activated protein kinase pathways to protect human vascular smooth muscle cells from apoptosis

29 October 2018

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29 October 2018

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29 October 2018

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29 October 2018

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12 December 2020

Regional overexpression of insulin-like growth factor-I and transforming growth factor-β1 in the myocardium of patients with hypertrophic obstructive cardiomyopathy

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12 December 2020

Myosin phosphorylation and the cross-bridge cycle in arterial smooth muscle

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12 December 2020

Flexibility of the myosin heavy chain: direct evidence that the region containing SH1 and SH2 can move 10 A under the influence of nucleotide binding

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12 December 2020

Familial thoracic aortic dilatations and dissections: a case control study

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12 December 2020

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12 December 2020

Activity of GH/IGF-I axis in patients with dilated cardiomyopathy

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12 December 2020

Identifiers

DOI

10.1093/HMG/DDM201

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17666408%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

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2 January 2020

PubMed publication ID

17666408

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