Genome-wide identification of pseudogenes capable of disease-causing gene conversion. (Q34521369)

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20 January 2020

title

Genome-wide identification of pseudogenes capable of disease-causing gene conversion (English)

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20 January 2020

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20 January 2020

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20 January 2020

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20 January 2020

Jared M Bischof

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20 January 2020

Annie P Chiang

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20 January 2020

Thomas L Casavant

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20 January 2020

Terry A Braun

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20 January 2020

publication date

1 June 2006

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20 January 2020

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20 January 2020

volume

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20 January 2020

issue

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20 January 2020

page(s)

545-552

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HOPPSIGEN: a database of human and mouse processed pseudogenes

20 January 2020

cites work

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7 January 2021

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

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7 January 2021

Immunoglobulin gene conversion: insights from bursal B cells and the DT40 cell line

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7 January 2021

The beta-esterase gene cluster of drosophila melanogaster: is psiEst-6 a pseudogene, a functional gene, or both?

1 reference

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7 January 2021

Physical location of the human immunoglobulin lambda-like genes, 14.1, 16.1, and 16.2

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7 January 2021

Homologues to the first gene for autosomal dominant polycystic kidney disease are pseudogenes

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7 January 2021

Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa

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7 January 2021

Homologous nonallelic recombinations between the iduronate-sulfatase gene and pseudogene cause various intragenic deletions and inversions in patients with mucopolysaccharidosis type II

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7 January 2021

A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene: implications for mutation analysis in pseudoxanthoma elasticum.

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7 January 2021

Folate pathway gene alterations in patients with neural tube defects

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7 January 2021

Gene conversion drives GC content evolution in mammalian histones

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7 January 2021

Frequent segmental sequence exchanges and rapid gene duplication characterize the MHC class I genes in lemurs

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7 January 2021

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders

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7 January 2021

An expressed pseudogene regulates the messenger-RNA stability of its homologous coding gene

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7 January 2021

Molecular mechanisms for genomic disorders

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7 January 2021

Connexin43 pseudogene is expressed in tumor cells and inhibits growth

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7 January 2021

The UCSC Genome Browser Database

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7 January 2021

Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa

1 reference

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7 January 2021

Neuronal expression of neural nitric oxide synthase (nNOS) protein is suppressed by an antisense RNA transcribed from an NOS pseudogene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20335

7 January 2021

Structural analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency

1 reference

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7 January 2021

Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction

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7 January 2021

Sequence Variability of a Human Pseudogene

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7 January 2021

A general model for genetic recombination

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7 January 2021

Mutations in the human lambda5/14.1 gene result in B cell deficiency and agammaglobulinemia

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7 January 2021

Novel SBDS mutations caused by gene conversion in Japanese patients with Shwachman-Diamond syndrome

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7 January 2021

Whole-genome screening indicates a possible burst of formation of processed pseudogenes and Alu repeats by particular L1 subfamilies in ancestral primates

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7 January 2021

Human Gene Mutation Database (HGMD): 2003 update

1 reference

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7 January 2021

Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease

1 reference

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7 January 2021

A novel missense mutation (837T-->C) in the phosphoglycerate kinase gene of a patient with a myopathic form of phosphoglycerate kinase deficiency.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20335

7 January 2021

Homozygous gene conversion in von Willebrand factor gene as a cause of type 3 von Willebrand disease and predisposition to inhibitor development

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20335

7 January 2021

A genome-wide survey of human pseudogenes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20335

7 January 2021

A unique form of autosomal dominant cataract explained by gene conversion between beta-crystallin B2 and its pseudogene

1 reference

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7 January 2021

Signatures of selection and gene conversion associated with human color vision variation

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7 January 2021

Gene conversion is a likely cause of mutation in PKD1.

1 reference

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7 January 2021

Large-scale analysis of pseudogenes in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20335

7 January 2021

Identifiers

DOI

10.1002/HUMU.20335

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16671097%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

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