Filamin B mutations cause chondrocyte defects in skeletal development (Q28302896)

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30 December 2019

title

Filamin B mutations cause chondrocyte defects in skeletal development (English)

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30 December 2019

1

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30 December 2019

Robert E. Lenkinski

3

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30 December 2019

Adele L. Boskey

8

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9

Christopher Walsh

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30 December 2019

author name string

Gewei Lian

2

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30 December 2019

Alec De Grand

4

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30 December 2019

R Roy Vaid

5

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30 December 2019

Thomas Bryce

6

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30 December 2019

Marina Stasenko

7

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30 December 2019

Volney Sheen

10

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30 December 2019

language of work or name

English

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publication date

17 May 2007

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30 December 2019

published in

Human Molecular Genetics

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30 December 2019

volume

16

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30 December 2019

issue

14

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30 December 2019

page(s)

1661-1675

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The many faces of filamin: a versatile molecular scaffold for cell motility and signalling

30 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Loss of FilaminC (FLNc) results in severe defects in myogenesis and myotube structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

A new member of the LIM protein family binds to filamin B and localizes at stress fibers

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Human beta-filamin is a new protein that interacts with the cytoplasmic tail of glycoprotein Ibalpha

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Different splice variants of filamin-B affect myogenesis, subcellular distribution, and determine binding to integrin [beta] subunits

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Filamins as integrators of cell mechanics and signalling

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Application of micro-CT assessment of 3-D bone microstructure in preclinical and clinical studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Molecular mechanisms of endochondral bone development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Loss of alpha10beta1 integrin expression leads to moderate dysfunction of growth plate chondrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Smad6/Smurf1 overexpression in cartilage delays chondrocyte hypertrophy and causes dwarfism with osteopenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Indian hedgehog signaling regulates proliferation and differentiation of chondrocytes and is essential for bone formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Reduced chondrocyte proliferation and chondrodysplasia in mice lacking the integrin-linked kinase in chondrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Growth defect in Grg5 null mice is associated with reduced Ihh signaling in growth plates

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Core-binding factor beta interacts with Runx2 and is required for skeletal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Runx2 and Runx3 are essential for chondrocyte maturation, and Runx2 regulates limb growth through induction of Indian hedgehog

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Bone morphogenetic protein type IA receptor signaling regulates postnatal osteoblast function and bone remodeling

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Bone morphogenetic protein receptor signaling is necessary for normal murine postnatal bone formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Perlecan maintains the integrity of cartilage and some basement membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Mice lacking link protein develop dwarfism and craniofacial abnormalities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Dmp1-deficient mice display severe defects in cartilage formation responsible for a chondrodysplasia-like phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Beta1 integrins regulate chondrocyte rotation, G1 progression, and cytokinesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Integrin expression by primary and immortalized human chondrocytes: evidence of a differential role for alpha1beta1 and alpha2beta1 integrins in mediating chondrocyte adhesion to types II and VI collagen

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Integrins: bidirectional, allosteric signaling machines

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Mutations in FLNB cause boomerang dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

New forms of neonatal death dwarfism. Report of 3 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Mutations in two regions of FLNB result in atelosteogenesis I and III.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Multiple congenital dislocations associated with characteristic facial abnormality

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Filamin B deficiency in mice results in skeletal malformations and impaired microvascular development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Increased filamin binding to beta-integrin cytoplasmic domains inhibits cell migration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Coordination of chondrocyte differentiation and joint formation by alpha5beta1 integrin in the developing appendicular skeleton.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Chondrocyte survival and differentiation in situ are integrin mediated.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Integrin-linked kinase regulates chondrocyte shape and proliferation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Function and interactions of integrins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Cytoskeletal protein ABP-280 directs the intracellular trafficking of furin and modulates proprotein processing in the endocytic pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Mutations of the ephrin-B1 gene cause craniofrontonasal syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Eph receptor-ephrin bidirectional signals that target Ras and Rho proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

The small GTPase RalA targets filamin to induce filopodia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

The Rac1- and RhoG-specific GEF domain of Trio targets filamin to remodel cytoskeletal actin

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

A somitic compartment of tendon progenitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

Apoptotic mechanisms in targeted neuronal cell death by chromophore-activated photolysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM114

21 January 2018

Identifiers

DOI

10.1093/HMG/DDM114

2 references

Consolidated OpenCitations Corpus – April 2017

2465187

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30 December 2019

2465187

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Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

2465187