(Q46349926)

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Developmental dysplasia of the hip: linkage mapping and whole exome sequencing identify a shared variant in CX3CR1 in all affected members of a large multigeneration family

scientific article published in December 2013

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scholarly article

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

Developmental dysplasia of the hip: linkage mapping and whole exome sequencing identify a shared variant in CX3CR1 in all affected members of a large multigeneration family (English)

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

1 reference

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Javad Parvizi

1 reference

Europe PubMed Central

21 December 2017

author name string

George J Feldman

1

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

Mark Levenstien

3

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

Kathryn Scott

4

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

Jill A Erickson

5

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

Paolo Fortina

6

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

Marcella Devoto

7

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

Christopher L Peters

8

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

publication date

1 December 2013

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

Journal of Bone and Mineral Research

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Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

28

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Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

12

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

2540-2549

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

Hip dysplasia and osteoarthrosis: a survey of 4151 subjects from the Osteoarthrosis Substudy of the Copenhagen City Heart Study.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Exclusion of COL2A1 and VDR as developmental dysplasia of the hip genes

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Developmental dysplasia of the hip: risk markers, clinical screening and outcome.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Congenital Dysplasia of the Hip in the Navajo Infant

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Perinatal risk factors for developmental dysplasia of the hip.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Familial predisposition to developmental dysplasia of the hip.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

The Otto Aufranc Award: Identification of a 4 Mb region on chromosome 17q21 linked to developmental dysplasia of the hip in one 18-member, multigeneration family

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Variable expression and incomplete penetrance of developmental dysplasia of the hip: clinical challenge in a 71-member multigeneration family.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

A statistical method for identification of polymorphisms that explain a linkage result

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Predicting deleterious amino acid substitutions

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Identifying a high fraction of the human genome to be under selective constraint using GERP++.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

A new class of membrane-bound chemokine with a CX3C motif

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Identification and molecular characterization of fractalkine receptor CX3CR1, which mediates both leukocyte migration and adhesion

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

The ENCODE (ENCyclopedia Of DNA Elements) Project

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

A user's guide to the encyclopedia of DNA elements (ENCODE)

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Microarray analysis of proliferative and hypertrophic growth plate zones identifies differentiation markers and signal pathways

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Microenvironmental changes during differentiation of mesenchymal stem cells towards chondrocytes.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Expression of CXC chemokines and their receptors is modulated during chondrogenic differentiation of human mesenchymal stem cells grown in three-dimensional scaffold: evidence in native cartilage.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

CX3CR1-dependent subretinal microglia cell accumulation is associated with cardinal features of age-related macular degeneration.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Genetics of resistance to HIV infection: Role of co-receptors and co-receptor ligands.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Polymorphisms of fractalkine receptor CX3CR1 gene in patients with symptomatic and asymptomatic carotid artery stenosis.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Loss of E2F4 activity leads to abnormal development of multiple cellular lineages

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Bone abnormalities in latent TGF-[beta] binding protein (Ltbp)-3-null mice indicate a role for Ltbp-3 in modulating TGF-[beta] bioavailability

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1999

21 January 2018

Identifiers

10.1002/JBMR.1999

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/23716478

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