Static respiratory cilia associated with mutations in Dnahc11/DNAH11: a mouse model of PCD (Q52159624)

25 April 2018

title

Static respiratory cilia associated with mutations in Dnahc11/DNAH11: a mouse model of PCD (English)

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25 April 2018

author name string

Jane S Lucas

1

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25 April 2018

Elizabeth C Adam

2

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Patricia M Goggin

3

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Claire L Jackson

4

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Nicola Powles-Glover

5

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Saloni H Patel

6

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James Humphreys

7

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Martin D Fray

8

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Emilie Falconnet

9

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Jean-Louis Blouin

10

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Michael T Cheeseman

11

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Lucia Bartoloni

12

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Dominic P Norris

13

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Peter M Lackie

14

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publication date

29 December 2011

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25 April 2018

published in

Human Mutation

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25 April 2018

volume

33

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issue

3

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25 April 2018

page(s)

495-503

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25 April 2018

Making sense of cilia in disease: the human ciliopathies.

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Primary ciliary dyskinesia: a consensus statement on diagnostic and treatment approaches in children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: implications for application to clinical testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

EMPReSS: standardized phenotype screens for functional annotation of the mouse genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Primary ciliary dyskinesia: current state of the art.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Ciliary beat pattern is associated with specific ultrastructural defects in primary ciliary dyskinesia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Mouse models of cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Flagellar assembly in two hundred and fifty easy-to-follow steps

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Mouse mutagenesis identifies novel roles for left-right patterning genes in pulmonary, craniofacial, ocular, and limb development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

The ciliary proteome database: an integrated community resource for the genetic and functional dissection of cilia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Ciliary dyskinesia with normal ultrastructure

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Development of the outflow tract. A study in hearts with situs solitus and situs inversus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Spectrum of heart malformations in mice with situs solitus, situs inversus, and associated visceral heterotaxy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Hydrocephalus, situs inversus, chronic sinusitis, and male infertility in DNA polymerase lambda-deficient mice: possible implication for the pathogenesis of immotile cilia syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Random determination of a developmental process: reversal of normal visceral asymmetry in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Primary ciliary dyskinesia in mice lacking the novel ciliary protein Pcdp1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Altered lung morphogenesis, epithelial cell differentiation and mechanics in mice deficient in the Wnt/β-catenin antagonist Chibby

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Fertility in men with primary ciliary dyskinesia presenting with respiratory infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

nm1054: a spontaneous, recessive, hypochromic, microcytic anemia mutation in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Abnormal nodal flow precedes situs inversus in iv and inv mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

A proteomic analysis of human cilia: identification of novel components

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Conditional deletion of dnaic1 in a murine model of primary ciliary dyskinesia causes chronic rhinosinusitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Nasal brushing for the study of ciliary ultrastructure

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Mutation of an axonemal dynein affects left-right asymmetry in inversus viscerum mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Mice deficient in the axonemal protein Tektin-t exhibit male infertility and immotile-cilium syndrome due to impaired inner arm dynein function

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Tubulin tyrosine ligase-like 1 deficiency results in chronic rhinosinusitis and abnormal development of spermatid flagella in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Accelerated mortality from hydrocephalus and pneumonia in mice with a combined deficiency of SPAG6 and SPAG16L reveals a functional interrelationship between the two central apparatus proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Determination of left–right patterning of the mouse embryo by artificial nodal flow

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

Situs inversus in homozygous mice without immotile cilia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

7 January 2021

https://api.crossref.org/works/10.1002%2FHUMU.22001

1 reference

7 January 2021

A 20-year experience of electron microscopy in the diagnosis of primary ciliary dyskinesia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

7 January 2021

New DNAH11 mutations in primary ciliary dyskinesia with normal axonemal ultrastructure

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22001

7 January 2021

Identifiers

DOI

10.1002/HUMU.22001

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25 April 2018

PubMed ID

22102620

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25 April 2018