Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss. (Q34975356)

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25 January 2020

title

Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss (English)

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25 January 2020

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Fernando Mayo-Merino

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Luis Augusto Aguirre Pérez

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Ignacio del Castillo

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Tamas Dalmay

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Karen P Steel

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author name string

Angeles Mencía

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Silvia Modamio-Høybjør

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Nick Redshaw

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Leticia Olavarrieta

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Felipe Moreno

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Miguel Angel Moreno-Pelayo

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language of work or name

English

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publication date

12 April 2009

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25 January 2020

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volume

41

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page(s)

609-613

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25 January 2020

issue

5

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https://scigraph.springernature.com/pub.10.1038/ng.355

25 January 2020

exact match

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cites work

MicroRNAs: small RNAs with a big role in gene regulation

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12 December 2020

Carbodiimide-mediated cross-linking of RNA to nylon membranes improves the detection of siRNA, miRNA and piRNA by northern blot

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A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci

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MicroRNA expression in zebrafish embryonic development

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A deletion involving the connexin 30 gene in nonsyndromic hearing impairment

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Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets

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Single nucleotide polymorphism associated with mature miR-125a alters the processing of pri-miRNA.

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Sequence variants in SLITRK1 are associated with Tourette's syndrome

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A common polymorphism in serotonin receptor 1B mRNA moderates regulation by miR-96 and associates with aggressive human behaviors

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An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice

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MicroRNA gene expression in the mouse inner ear.

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A mutation creating a potential illegitimate microRNA target site in the myostatin gene affects muscularity in sheep

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Human microRNA-155 on chromosome 21 differentially interacts with its polymorphic target in the AGTR1 3' untranslated region: a mechanism for functional single-nucleotide polymorphisms related to phenotypes

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Effects of a neuregulin 1 variant on conversion to schizophrenia and schizophreniform disorder in people at high risk for psychosis

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Crossref

https://api.crossref.org/works/10.1038%2FNG.355

7 January 2021

inferred from DOI database lookup

Human MicroRNA targets

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.355

7 January 2021