(Q36484332)

English

Human cytomegalovirus (HCMV) and hearing impairment: infection of fibroblast cells with HCMV induces chromosome breaks at 1q23.3, between loci DFNA7 and DFNA49 -- both involved in dominantly inherited, sensorineural, hearing impairment

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scholarly article

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Europe PubMed Central

PMC publication ID

14 August 2017

Human cytomegalovirus (HCMV) and hearing impairment: infection of fibroblast cells with HCMV induces chromosome breaks at 1q23.3, between loci DFNA7 and DFNA49 -- both involved in dominantly inherited, sensorineural, hearing impairment (English)

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Europe PubMed Central

PMC publication ID

14 August 2017

Cytomegalovirus

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Øivind Nilssen

5

object named as

Øivind Nilssen

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Toril Fagerheim

2

object named as

Toril Fagerheim

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

3

object named as

Vigdis Brox

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

author name string

Mona Nystad

1

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Europe PubMed Central

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14 August 2017

Elizabeth A Fortunato

4

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Europe PubMed Central

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14 August 2017

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publication date

25 July 2007

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Europe PubMed Central

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14 August 2017

Mutation Research

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Europe PubMed Central

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14 August 2017

637

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Europe PubMed Central

PMC publication ID

14 August 2017

1-2

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

56-65

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Human cytomegalovirus disrupts both ataxia telangiectasia mutated protein (ATM)- and ATM-Rad3-related kinase-mediated DNA damage responses during lytic infection

1 reference

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30 September 2017

Mechanisms of common fragile site instability.

1 reference

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30 September 2017

Long-range control of gene expression: emerging mechanisms and disruption in disease

1 reference

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30 September 2017

Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease

1 reference

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30 September 2017

DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

30 September 2017

Viral induction of site-specific chromosome damage.

1 reference

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30 September 2017

Infection of cells with human cytomegalovirus during S phase results in a blockade to immediate-early gene expression that can be overcome by inhibition of the proteasome

1 reference

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30 September 2017

The terminase subunits pUL56 and pUL89 of human cytomegalovirus are DNA-metabolizing proteins with toroidal structure

1 reference

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30 September 2017

Congenital CMV-infection and hearing loss.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

30 September 2017

An axonal form of Charcot-Marie-Tooth disease showing distinctive features in association with mutations in the peripheral myelin protein zero gene (Thr124Met or Asp75Val).

1 reference

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30 September 2017

Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa

1 reference

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30 September 2017

Exploitation of cellular signaling and regulatory pathways by human cytomegalovirus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

30 September 2017

Specific chromosome 1 breaks induced by human cytomegalovirus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

30 September 2017

Report on a long-term study of maternal and congenital cytomegalovirus infection in Sweden. Review of prospective studies available in the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

30 September 2017

Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

30 September 2017

Cell cycle dysregulation by human cytomegalovirus: influence of the cell cycle phase at the time of infection and effects on cyclin transcription.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

30 September 2017

p53 and RPA are sequestered in viral replication centers in the nuclei of cells infected with human cytomegalovirus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

30 September 2017

Auditory neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

30 September 2017

Generation of a new adenovirus type 12-inducible fragile site by insertion of an artificial U2 locus in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

30 September 2017

Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

30 September 2017

Construction of a cloned library of the EcoRI fragments from the human cytomegalovirus genome (strain AD169)

1 reference

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30 September 2017

Cytomegalovirus Isolation from a Human Inner Ear

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

30 September 2017

Pathology and physiology of auditory neuropathy with a novel mutation in the MPZ gene (Tyr145->Ser).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

28 June 2018

Late intrauterine Cytomegalovirus infection: clinical and neuroimaging findings

1 reference

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28 June 2018

Mondini dysplasia and congenital cytomegalovirus infection.

1 reference

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28 June 2018

Proposed nomenclature for PNS myelin proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

28 June 2018

Chromosomal fragility, structural rearrangements and mobile element activity may reflect dynamic epigenetic mechanisms of importance in neurobehavioural genetics

1 reference

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21 September 2018

Cytomegalovirus in the perilymphatic fluid.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

21 September 2018

A wider role for congenital cytomegalovirus infection in sensorineural hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

21 September 2018

Detection of human cytomegalovirus DNA in perilymph of patients with sensorineural hearing loss using real-time PCR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

21 September 2018

Abnormal white matter lesions with sensorineural hearing loss caused by congenital cytomegalovirus infection: retrospective diagnosis by PCR using Guthrie cards

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

21 September 2018

Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian family.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2259117

21 September 2018

Dominant modifier DFNM1 suppresses recessive deafness DFNB26

1 reference

https://pubmed.ncbi.nlm.nih.gov/17765268

12 December 2020

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10.1016/J.MRFMMM.2007.07.009

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

ResearchGate publication ID

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