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Article

Generation of a human iPSC line from a patient with retinitis pigmentosa caused by mutation in PRPF8 gene.

Stem cell research - 1 May 2017

Lukovic Dunja, Bolinches-Amorós Arantxa, Artero-Castro Ana, Pascual Beatriz, Carballo Miguel, Hernan Imma, Erceg Slaven

Abstract excerpt

The human iPSC cell line, RP2-FiPS4F1 (RCPFi001-A), derived from dermal fibroblasts from the patient with retinitis pigmentosa caused by the mutation of the gene PRPF8, was generated by non-integrative reprogramming technology using OCT3/4, SOX2, CMYC and KLF4 reprogramming factors.

Read the complete abstract on PubMed

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 28677533
DOI: 10.1016/j.scr.2017.03.007

Genes

PRPF8
KLF4
SOX2

Provenance

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

Related research

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Research trail→

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Generation of a human iPSC line from a patient with retinitis pigmentosa caused by mutation in PRPF8 gene.PMID 28677533Read ↗

Establishment of induced pluripotent stem cell line CSUASOi004-A by reprogramming peripheral blood mononuclear cells of a PRPF6-related dominant retinitis pigmentosa patient.Semantic proximity Read ↗

Establishment of an induced pluripotent stem (iPS) cell line from dermal fibroblasts of an asymptomatic patient with dominant PRPF31 mutation.Semantic proximity Read ↗

Generation of a gene-corrected isogenic human iPSC line (CSUASOi006-A-1) from a retinitis pigmentosa patient with heterozygous c.5792C > T mutation in the PRPF8 gene.Semantic proximity Read ↗

Generation of a gene-corrected human iPSC line (CSUASOi004-A-1) from a retinitis pigmentosa patient with heterozygous c.2699 G>A mutation in the PRPF6 gene.Semantic proximity Read ↗

Establishment of CSUASOi014-A, an induced pluripotent stem cell line from blood-derived cells of a Chinese patient carrying PRPF31 gene mutation.Semantic proximity Read ↗

Generation of three human iPSC lines from a retinitis pigmentosa family with SLC7A14 mutation.Semantic proximity Read ↗

Generation of the induced pluripotent stem cell line IOCVi001-A from a patient with the MFRP-related retinitis pigmentosa-nanophthalmos syndrome.Semantic proximity Read ↗

Establishment of non-integrate induced pluripotent stem cell line CSUASOi006-A, from urine-derived cells of a PRPF8-related dominant retinitis pigmentosa patient.Semantic proximity Read ↗

Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 gene.Semantic proximity Read ↗

CRISPR/Cas9-mediated generation of a human induced pluripotent stem cell line with PRPF6 c.2699 G > A mutation to model retinitis pigmentosa.Semantic proximity Read ↗

Generation of a human iPSC line, INMi005-A, from a patient with non-syndromic USH2A-associated retinitis pigmentosa.Semantic proximity Read ↗

Generation of two induced pluripotent stem cell lines (RCMGi004-A and -B) from human skin fibroblasts of a cystic fibrosis patient with compound heterozygous F508del/W1282X mutations in CFTR gene.Semantic proximity Read ↗

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