(Q37091888)

18 August 2017

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title

Fibrillin-rich microfibrils - structural and instructive determinants of mammalian development and physiology (English)

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18 August 2017

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Francesco Ramirez

1

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18 August 2017

Luca Carta

2

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18 August 2017

Sui Lee-Arteaga

3

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18 August 2017

Catherine Liu

4

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18 August 2017

Harikiran Nistala

5

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18 August 2017

Silvia Smaldone

6

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18 August 2017

publication date

1 January 2008

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Connective Tissue Research

18 August 2017

published in

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18 August 2017

volume

49

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18 August 2017

issue

1

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18 August 2017

page(s)

1-6

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Fibrillin microfibrils: multipurpose extracellular networks in organismal physiology

18 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F03008200701820708

Fibrillins: from biogenesis of microfibrils to signaling functions.

21 January 2018

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21 January 2018

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Marfan syndrome: from molecular pathogenesis to clinical treatment

21 January 2018

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Latent transforming growth factor beta-binding protein 1 interacts with fibrillin and is a microfibril-associated protein

21 January 2018

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https://api.crossref.org/works/10.1080%2F03008200701820708

The prodomain of BMP-7 targets the BMP-7 complex to the extracellular matrix

21 January 2018

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Probing substrate binding site of the Escherichia coli quinol oxidases using synthetic ubiquinol analogues.

21 January 2018

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https://api.crossref.org/works/10.1080%2F03008200701820708

Homo- and heterotypic fibrillin-1 and -2 interactions constitute the basis for the assembly of microfibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F03008200701820708

alphaVbeta6 is a novel receptor for human fibrillin-1. Comparative studies of molecular determinants underlying integrin-rgd affinity and specificity

21 January 2018

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https://api.crossref.org/works/10.1080%2F03008200701820708

Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome

21 January 2018

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Congenital contractural arachnodactyly (Beals syndrome).

21 January 2018

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Marfan syndrome: orthopedic and genetic review

21 January 2018

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Extracellular matrix in vascular morphogenesis and disease: structure versus signal

21 January 2018

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Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome.

21 January 2018

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Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1

21 January 2018

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Evidence for a critical contribution of haploinsufficiency in the complex pathogenesis of Marfan syndrome

21 January 2018

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Fibrillins 1 and 2 perform partially overlapping functions during aortic development

21 January 2018

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Regulation of limb patterning by extracellular microfibrils

21 January 2018

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Neural crest and cardiovascular development: a 20-year perspective

21 January 2018

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https://api.crossref.org/works/10.1080%2F03008200701820708

Developmental expression of fibrillin genes suggests heterogeneity of extracellular microfibrils

21 January 2018

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https://api.crossref.org/works/10.1080%2F03008200701820708

Fibrillin-1 and fibrillin-2 in human embryonic and early fetal development

21 January 2018

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Symposium on the musculoskeletal aspects of Marfan syndrome: meeting report and state of the science

21 January 2018

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Interdigital regulation of digit identity and homeotic transformation by modulated BMP signaling

21 January 2018

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Control of osteoblast function and regulation of bone mass

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.1080%2F03008200701820708

Neutralization of transforming growth factor-beta attenuates hypertension and prevents renal injury in uremic rats

21 January 2018

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https://api.crossref.org/works/10.1080%2F03008200701820708

Angiotensin II type 1 receptor blockade attenuates TGF-beta-induced failure of muscle regeneration in multiple myopathic states

21 January 2018

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

21 January 2018

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Aneurysm syndromes caused by mutations in the TGF-beta receptor

21 January 2018

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https://api.crossref.org/works/10.1080%2F03008200701820708

Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F03008200701820708

10.1080/03008200701820708

21 January 2018

Identifiers

DOI

1 reference

18 August 2017

1 reference