Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia (Q24302250)

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

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scholarly article

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Europe PubMed Central

PubMed publication ID

5 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

Dynein axonemal heavy chain 11

1 reference

GOA release 2020-03-11

determination of left/right symmetry

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GOA release 2020-03-11

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

primary ciliary dyskinesia

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based on heuristic

inferred from title

Stilianos Antonarakis

15

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Europe PubMed Central

PubMed publication ID

5 July 2017

author name string

Lucia Bartoloni

1

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Europe PubMed Central

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5 July 2017

Jean-Louis Blouin

2

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Europe PubMed Central

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5 July 2017

Yanzhen Pan

3

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Europe PubMed Central

PubMed publication ID

5 July 2017

Corinne Gehrig

4

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Europe PubMed Central

PubMed publication ID

5 July 2017

Amit K Maiti

5

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Europe PubMed Central

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5 July 2017

Nathalie Scamuffa

6

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Europe PubMed Central

PubMed publication ID

5 July 2017

Colette Rossier

7

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Europe PubMed Central

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5 July 2017

Mark Jorissen

8

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Europe PubMed Central

PubMed publication ID

5 July 2017

Miguel Armengot

9

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Europe PubMed Central

PubMed publication ID

5 July 2017

Maggie Meeks

10

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Europe PubMed Central

PubMed publication ID

5 July 2017

Hannah M Mitchison

11

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5 July 2017

Eddie M K Chung

12

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Europe PubMed Central

PubMed publication ID

5 July 2017

Celia D Delozier-Blanchet

13

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Europe PubMed Central

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5 July 2017

William J Craigen

14

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PubMed publication ID

5 July 2017

language of work or name

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publication date

25 July 2002

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

Proceedings of the National Academy of Sciences of the United States of America

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PubMed publication ID

5 July 2017

99

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Europe PubMed Central

PubMed publication ID

5 July 2017

16

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Europe PubMed Central

PubMed publication ID

5 July 2017

10282-10286

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Europe PubMed Central

PubMed publication ID

5 July 2017

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

19 March 2017

Disruption of an inner arm dynein heavy chain gene results in asthenozoospermia and reduced ciliary beat frequency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

19 March 2017

Initial sequencing and analysis of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

19 March 2017

Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

19 March 2017

The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

19 March 2017

Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

19 March 2017

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

19 March 2017

The Sequence of the Human Genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

19 March 2017

Targeted deletion of the ATP binding domain of left-right dynein confirms its role in specifying development of left-right asymmetries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

19 March 2017

Germline mutations in an intermediate chain dynein cause primary ciliary dyskinesia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

27 September 2017

Clinical aspects of defects in the determination of laterality

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

27 September 2017

The dynein heavy chain: structure, mechanics and evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

27 September 2017

Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

27 September 2017

No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with primary ciliary dyskinesia (PCD).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

27 September 2017

Insights into the structural organization of the I1 inner arm dynein from a domain analysis of the 1beta dynein heavy chain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

27 September 2017

The Staden sequence analysis package

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

27 September 2017

Exploring the function of inner and outer dynein arms with Chlamydomonas mutants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

27 September 2017

DYNEINS: molecular structure and cellular function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

27 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

27 September 2017

Genetical and ultrastructural aspects of the immotile-cilia syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

27 September 2017

Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

30 May 2018

Identification of a microtubule-binding domain in a cytoplasmic dynein heavy chain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

30 May 2018

Ciliogenesis in cultured human nasal epithelium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

30 May 2018

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124905

30 May 2018

Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile cilia

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.152337699

21 January 2018

Abnormal nodal flow precedes situs inversus in iv and inv mice

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.152337699

21 January 2018

Model for the motor component of dynein heavy chain based on homology to the AAA family of oligomeric ATPases

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.152337699

21 January 2018

New developments in the diagnosis of Kartagener's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/12142464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.152337699

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

2002PNAS...9910282B

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

ResearchGate publication ID

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