t/gene-ran

RAN gene

Discuss publications and research concerning the RAN gene.

0 members0 posts12 articles

Start the first discussion

Ask a question, share context or link a publication.

Topic rules

Follow Noodle’s community and scientific integrity rules.

Moderators

Managed by the Noodle moderation team.

Related literature

Variable Phenotype in Three Siblings With RAN Binding Protein 2 Variant With Potential Preventive Treatment for Recurrences.
RAN
Polymorphic CGG repeats in gene regulation and disease.
RAN
Single nucleotide polymorphisms of GEMIN3 modify the risk of primary Sjögren's syndrome in female patients.
RAN
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.
RAN
Repeat-Associated Non-ATG Translation in Neurological Diseases.
RAN
[Recent Topics in Autosomal Dominantly Inherited Spinocerebellar Ataxias].
RAN
Understanding decreased fertility in women carriers of the FMR1 premutation: a possible mechanism for Fragile X-Associated Primary Ovarian Insufficiency (FXPOI).
RAN
Beyond loss of frataxin: the complex molecular pathology of Friedreich ataxia.
RAN
Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS.
RAN
Outcomes of empirical eating disorder phenotypes in a clinical female sample: results from a latent class analysis.
RAN

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details