Analysis of nuclear and mitochondrial genes in patients with pseudoexfoliation glaucoma. (Q36489206)

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2 January 2020

title

Analysis of nuclear and mitochondrial genes in patients with pseudoexfoliation glaucoma (English)

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2 January 2020

author name string

Khaled K Abu-Amero

series ordinal

1

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2 January 2020

Thomas M Bosley

series ordinal

2

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2 January 2020

Jose Morales

series ordinal

3

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2 January 2020

publication date

10 January 2008

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2 January 2020

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2 January 2020

volume

14

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2 January 2020

page(s)

29-36

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Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma

2 January 2020

cites work

1 reference

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Mitochondrial abnormalities in patients with LHON-like optic neuropathies

30 September 2017

1 reference

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Increased relative mitochondrial DNA content in leucocytes of patients with NAION.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

Association of mitochondrial DNA transversion mutations with familial medullary thyroid carcinoma/multiple endocrine neoplasia type 2 syndrome

30 September 2017

1 reference

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Hereditary optic neuropathies: from the mitochondria to the optic nerve

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

Mitochondrial DNA mutations and mitochondrial DNA depletion in gastric cancer

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

MITOMAP: a human mitochondrial genome database--2004 update

30 September 2017

1 reference

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Increase of mitochondrial DNA in blood cells of patients with Leber's hereditary optic neuropathy with 11778 mutation

30 September 2017

1 reference

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A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy

30 September 2017

1 reference

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Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

Pseudoexfoliation syndrome in Icelandic families

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

Prediction of deleterious human alleles

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

Mitochondrial DNA analysis: polymorphisms and pathogenicity

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

Role of CYP1B1, MYOC, OPTN, and OPTC genes in adult-onset primary open-angle glaucoma: predominance of CYP1B1 mutations in Indian patients

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

Association of pseudoexfoliation syndrome with increased vascular risk.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

Assessment of neuronal viability with Alamar blue in cortical and granule cell cultures.

28 June 2018

1 reference

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Oxygen requirements of yeasts

28 June 2018

1 reference

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What is a 'novel' mtDNA mutation--and does 'novelty' really matter?

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

Detection of mitochondrial respiratory dysfunction in circulating lymphocytes using resazurin

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

Sperm mitochondrial DNA depletion in men with asthenospermia.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

Impaired mitochondrial function, oxidative stress and altered antioxidant enzyme activities following traumatic spinal cord injury.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2263010

Mitochondrial DNA nucleotide changes in non-arteritic ischemic optic neuropathy

21 September 2018

1 reference

12 December 2020

Pseudoexfoliation syndrome. Ocular manifestation of a systemic disorder?

1 reference

12 December 2020

Pseudoexfoliative fibrillopathy in visceral organs of a patient with pseudoexfoliation syndrome

1 reference

12 December 2020

Generalized transluminance of the iris and the frequency of the pseudoexfoliation syndrome in the eyes of transient ischemic attack patients

1 reference

12 December 2020

Molecular mechanisms in mitochondrial DNA depletion syndrome

1 reference

12 December 2020

Is pseudoexfoliation syndrome inherited? A review of genetic and nongenetic factors and a new observation

1 reference

12 December 2020

Familial occurrence of pseudoexfoliation in Canada

1 reference

12 December 2020

Mitochondrial abnormalities in patients with primary open-angle glaucoma

1 reference

12 December 2020

Early diagnosis of exfoliation syndrome in the offspring of affected patients

1 reference

12 December 2020

Mitochondrial changes in leukocytes of patients with optic neuritis

1 reference

12 December 2020

Nuclear and mitochondrial analysis of patients with primary angle-closure glaucoma

1 reference

12 December 2020

Identifiers

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18246027%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

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