(Q30354085)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643886%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

review article

1 reference

title

Hearts and bones: shared regulatory mechanisms in heart valve, cartilage, tendon, and bone development (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643886%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643886%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

author name string

Joy Lincoln

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643886%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Alexander W Lange

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643886%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

language of work or name

English

0 references

publication date

27 April 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643886%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

published in

Developmental Biology

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643886%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

volume

294

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643886%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643886%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

page(s)

292-302

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643886%20AND%20SRC:MED&resulttype=core&format=json

Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy)

20 January 2020

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Ultrastructure abnormalities in proteoglycans, collagen fibrils, and elastic fibers in normal and myxomatous mitral valve chordae tendineae

7 January 2021

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The transcription factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6

7 January 2021

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Essential role of Sox9 in the pathway that controls formation of cardiac valves and septa

7 January 2021

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Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation

7 January 2021

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Perlecan is essential for cartilage and cephalic development

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Heart valve development: endothelial cell signaling and differentiation

7 January 2021

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CD34+ fibrocytes in normal mitral valves and myxomatous mitral valve degeneration

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Genetic and cellular analyses of zebrafish atrioventricular cushion and valve development

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SOX9 directly regulates the type-II collagen gene

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Sox9 is required for cartilage formation

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FGF acts directly on the somitic tendon progenitors through the Ets transcription factors Pea3 and Erm to regulate scleraxis expression

7 January 2021

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Chondrocyte-specific enhancer elements in the Col11a2 gene resemble the Col2a1 tissue-specific enhancer

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Aortic root dilatation and mitral valve prolapse in Marfan's syndrome: an ECHOCARDIOgraphic study

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osteoprotegerin-deficient mice develop early onset osteoporosis and arterial calcification

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Tenascin-X deficiency is associated with Ehlers-Danlos syndrome

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Endogenous and ectopic expression of noggin suggests a conserved mechanism for regulation of BMP function during limb and somite patterning

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Longevity and lineages: toward the integrative biology of degenerative diseases in heart, muscle, and bone

7 January 2021

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Analysis of the molecular cascade responsible for mesodermal limb chondrogenesis: Sox genes and BMP signaling.

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Chick myotendinous antigen. I. A monoclonal antibody as a marker for tendon and muscle morphogenesis

7 January 2021

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Hyperplastic conotruncal endocardial cushions and transposition of great arteries in perlecan-null mice.

7 January 2021

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Bicuspid aortic valve is heritable

7 January 2021

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Lineage and morphogenetic analysis of the cardiac valves.

7 January 2021

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Role of the NF-ATc transcription factor in morphogenesis of cardiac valves and septum

7 January 2021

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Control of endocardial cushion and cardiac valve maturation by BMP signaling pathways

7 January 2021

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Recent progress towards a molecular understanding of Marfan syndrome

7 January 2021

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Signals regulating tendon formation during chick embryonic development

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Fgf4 positively regulates scleraxis and tenascin expression in chick limb tendons

7 January 2021

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Molecular regulation of atrioventricular valvuloseptal morphogenesis

7 January 2021

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

7 January 2021

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

7 January 2021

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In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome

7 January 2021

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Extracellular matrix remodelling in human aortic valve disease: the role of matrix metalloproteinases and their tissue inhibitors

7 January 2021

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Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene

7 January 2021

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Mutations in NOTCH1 cause aortic valve disease

7 January 2021

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Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency

7 January 2021

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Molecular markers of cardiac endocardial cushion development.

7 January 2021

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Nf1 has an essential role in endothelial cells

7 January 2021

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

7 January 2021

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Cathepsin K Knockout Mice Develop Osteopetrosis Due to a Deficit in Matrix Degradation but Not Demineralization

7 January 2021

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Marshall syndrome associated with a splicing defect at the COL11A1 locus

7 January 2021

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Developmental expression of perlecan during murine embryogenesis

7 January 2021

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Versican expression is associated with chamber specification, septation, and valvulogenesis in the developing mouse heart.

7 January 2021

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The calcineurin/nuclear factor of activated T cells signaling pathway regulates osteoclastogenesis in RAW264.7 cells

7 January 2021

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The incidence of congenital heart disease

7 January 2021

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The extracellular matrix architecture relating to myotendinous pattern formation in the distal part of the developing chick limb: an ultrastructural, histochemical and immunocytochemical analysis

7 January 2021

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Elastic extracellular matrix of the embryonic chick heart: an immunohistological study using laser confocal microscopy

7 January 2021

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Atrioventricular valves of the mouse: III. Collagenous skeleton and myotendinous junction

7 January 2021

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Critical roles of c-Jun signaling in regulation of NFAT family and RANKL-regulated osteoclast differentiation

7 January 2021

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Survey of fibroblast growth factor expression during chick organogenesis.

7 January 2021

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Reaching a genetic and molecular understanding of skeletal development

7 January 2021

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Conditional inactivation of Sox9: a mouse model for campomelic dysplasia.

7 January 2021

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Expression of type VI collagen in the developing mouse heart

7 January 2021

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OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis

7 January 2021

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SOX9-dependent and -independent transcriptional regulation of human cartilage link protein

7 January 2021

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Noonan syndrome mutation Q79R in Shp2 increases proliferation of valve primordia mesenchymal cells via extracellular signal-regulated kinase 1/2 signaling.

7 January 2021

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NFATc1 expression in the developing heart valves is responsive to the RANKL pathway and is required for endocardial expression of cathepsin K.

7 January 2021

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Structural and genetic bases of arterial stiffness.

7 January 2021

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Identification of the molecular defect in a family with spondyloepiphyseal dysplasia

7 January 2021

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Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes

7 January 2021

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SOX9 is a potent activator of the chondrocyte-specific enhancer of the pro alpha1(II) collagen gene

7 January 2021

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A fibrillar collagen gene, Col11a1, is essential for skeletal morphogenesis

7 January 2021

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Novel arterial pathology in mice and humans hemizygous for elastin

7 January 2021

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RANK is the intrinsic hematopoietic cell surface receptor that controls osteoclastogenesis and regulation of bone mass and calcium metabolism

7 January 2021

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Relationship between collagen fibrils, glycosaminoglycans, and stress relaxation in mitral valve chordae tendineae

7 January 2021

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MAP kinase activation in avian cardiovascular development

7 January 2021

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Prevalence of mitral-valve prolapse in the Stickler syndrome

7 January 2021

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Development of heart valve leaflets and supporting apparatus in chicken and mouse embryos

7 January 2021

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BMP and FGF regulatory pathways control cell lineage diversification of heart valve precursor cells.

7 January 2021

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Type III collagen is crucial for collagen I fibrillogenesis and for normal cardiovascular development

7 January 2021

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Identification of an enhancer sequence within the first intron required for cartilage-specific transcription of the alpha2(XI) collagen gene

7 January 2021

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Embryonic lethal mutation in mouse collagen I gene causes rupture of blood vessels and is associated with erythropoietic and mesenchymal cell death.

7 January 2021

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Bmp2 is essential for cardiac cushion epithelial-mesenchymal transition and myocardial patterning

7 January 2021

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Structural development of endocardial cushions

7 January 2021

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Essential role of p38 mitogen-activated protein kinase in cathepsin K gene expression during osteoclastogenesis through association of NFATc1 and PU.1

7 January 2021

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Severe osteoporosis in mice lacking osteoclastogenesis inhibitory factor/osteoprotegerin

7 January 2021

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The Cspg2 gene, disrupted in the hdf mutant, is required for right cardiac chamber and endocardial cushion formation

7 January 2021

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Bone formation and inflammation in cardiac valves

7 January 2021

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Expression of Sox8, Sox9 and Sox10 in the developing valves and autonomic nerves of the embryonic heart

7 January 2021

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Williams syndrome: autosomal dominant inheritance

7 January 2021

1 reference

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Fibrillin and other matrix proteins in mitral valve prolapse syndrome.

7 January 2021

1 reference

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SOX9 binds DNA, activates transcription, and coexpresses with type II collagen during chondrogenesis in the mouse

7 January 2021

1 reference

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Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia).

7 January 2021

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Classical Ehlers-Danlos syndrome caused by a mutation in type I collagen

7 January 2021

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Cell biology of cardiac cushion development.

7 January 2021

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Activated interstitial myofibroblasts express catabolic enzymes and mediate matrix remodeling in myxomatous heart valves

7 January 2021

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Human Aortic Valve Calcification Is Associated With an Osteoblast Phenotype

7 January 2021

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The transcription factor NF-ATc is essential for cardiac valve formation

7 January 2021

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Immunohistological and ultrastructural study of the developing tendons of the avian foot

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Impaired osteoclastic bone resorption leads to osteopetrosis in cathepsin-K-deficient mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency

7 January 2021

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Cardiac valves and valvular pathology: update on function, disease, repair, and replacement

7 January 2021

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Form and function of developing heart valves: coordination by extracellular matrix and growth factor signaling

7 January 2021

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Aortic valve cusp microstructure: The role of elastin

7 January 2021

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Feedback interactions between MKP3 and ERK MAP kinase control scleraxis expression and the specification of rib progenitors in the developing chick somite

7 January 2021

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Stickler syndrome: Correlation between vitreoretinal phenotypes and linkage to COL 2A1

7 January 2021

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Stickler syndrome type 2 and linkage to the COL11A1 gene

7 January 2021

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Expression of MMP2, MMP9, MT1-MMP, TIMP1, and TIMP2 mRNA in valvular lesions of the heart

7 January 2021

1 reference

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Fibroblast growth factor (FGF)-4 can induce proliferation of cardiac cushion mesenchymal cells during early valve leaflet formation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Bone morphogenetic protein-2 can mediate myocardial regulation of atrioventricular cushion mesenchymal cell formation in mice

7 January 2021

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The epidemiology of valvular heart diseases: the problem is growing

7 January 2021

1 reference

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Induction and activation of the transcription factor NFATc1 (NFAT2) integrate RANKL signaling in terminal differentiation of osteoclasts

7 January 2021

1 reference

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Abnormalities in elastic fibers and other connective-tissue components of floppy mitral valve

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

The molecular triad OPG/RANK/RANKL: involvement in the orchestration of pathophysiological bone remodeling

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Heart disease and stroke statistics--2006 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Molecular basis of vertebrate limb patterning

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesis imperfecta

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Expression of a partially deleted gene of human type II procollagen (COL2A1) in transgenic mice produces a chondrodysplasia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

The role of elastin in aortic valve mechanics

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Heart valve tissue engineering

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Valvular myofibroblast activation by transforming growth factor-beta: implications for pathological extracellular matrix remodeling in heart valve disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

UDP-glucose dehydrogenase required for cardiac valve formation in zebrafish.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Mice lacking link protein develop dwarfism and craniofacial abnormalities.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Dwarfism and age-associated spinal degeneration of heterozygote cmd mice defective in aggrecan

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Marfan syndrome and mitral valve prolapse

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Limb chondrogenesis is compromised in the versican deficient hdf mouse

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Multiple functions of BMPs in chondrogenesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Developmental pattern of expression of the mouse alpha 1 (XI) collagen gene (Col11a1).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.03.027

Cutis laxa arising from frameshift mutations in exon 30 of the elastin gene (ELN)

7 January 2021

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