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Article

Molecular mechanisms of photoreceptor degeneration in RP caused by IMPDH1 mutations.

Advances in experimental medicine and biology - 1 Jan 2006

Aherne Aileen, Kennan Avril, Kenna Paul F, McNally Niamh, Farrar G Jane, Humphries Pete

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Topics

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Share to DNA, Complementary
Share to Electroretinography
Share to Gene Expression Regulation
Share to IMP Dehydrogenase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mice, Inbred C57BL

Share to Mice, Transgenic

Share to Photoreceptor Cells

Share to Retinitis Pigmentosa

Source

Identifiers

PMID: 17249559
DOI: 10.1007/0-387-32442-9_13

Genes

IMPDH1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

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Molecular mechanisms of photoreceptor degeneration in RP caused by IMPDH1 mutations.PMID 17249559Read ↗

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Why Do Mutations in the Ubiquitously Expressed Housekeeping Gene<i>IMPDH1</i>Cause Retina-Specific Photoreceptor Degeneration?Semantic proximity Read ↗

On the molecular pathology of neurodegeneration in IMPDH1-based retinitis pigmentosaSemantic proximity Read ↗

Discovery of a Novel Missense Mutation in the RIMS1 Gene Potentially Enhances the Severity of Retinitis Pigmentosa (RP) Caused by RP1 Mutation in HumansSemantic proximity Read ↗

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