Cell line · CVCL_ZP35
C5RO
Finite cell line, Homo sapiens. 16 papers.
4 sourcescell-lines-2026-11-14-0.1.0
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Cite this record
ConductScience Library. C5RO. Cell lines, record CVCL_ZP35. Release cell-lines-2026-11-14-0.1.0, 14 Nov 2026. https://conductscience.org/library/cell-lines/CVCL_ZP35
On this page
Cell line
As Cellosaurus gives it.
- Name
- C5RO
- Accession
- CVCL_ZP35
- RRID
- RRID:CVCL_ZP35
- Synonyms
- Control 5 ROtterdam
- Species
- Homo sapiens (Human)
- Sex
- Female
- Age at sampling
- 30Y
- Category
- Finite cell line
- Derived from
- Skin (in situ)
- Cell type
- Fibroblast of skin
- Entry created
- 2020-07-02
- Entry updated
- 2023-06-29
Source Cellosaurus
Problems0
Cellosaurus records no problem for this cell line.
None in this release.
Papers16
| Paper | Journal | Year | How we know | Retracted | Source |
|---|---|---|---|---|---|
| Crosstalk between chromatin state and ATM signalling in DNA damage-induced transcription stress. | EMBO J | 2025 | Its Methods give the RRID and name the line | PubMed | |
| Curcumin Induces Homologous Recombination Deficiency by BRCA2 Degradation in Breast Cancer and Normal Cells. | Cancers (Basel) | 2025 | Its Methods give the RRID and name the line | PubMed | |
| Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype. | Am J Hum Genet | 2019 | Cellosaurus cites it | PubMed | |
| Mislocalization of XPF-ERCC1 nuclease contributes to reduced DNA repair in XP-F patients. | PLoS Genet | 2010 | Cellosaurus cites it | PubMed | |
| First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure. | Am J Hum Genet | 2007 | Cellosaurus cites it | PubMed | |
| A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A. | Nat Genet | 2004 | Cellosaurus cites it | PubMed | |
| Oxidative stress in cancer prone xeroderma pigmentosum fibroblasts. Real-time and single cell monitoring of superoxide and nitric oxide production with microelectrodes. | Carcinogenesis | 2004 | Cellosaurus cites it | PubMed | |
| Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients. | J Invest Dermatol | 2002 | Cellosaurus cites it | PubMed | |
| Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease. | J Invest Dermatol | 1998 | Cellosaurus cites it | PubMed | |
| A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy. | Am J Hum Genet | 1997 | Cellosaurus cites it | PubMed |
1 to 10 of 16
See all 16 papersRelatives2
| Relation | Cell line | Accession | Problem | Source |
|---|---|---|---|---|
| Derived from it | C5RO-hTERT | CVCL_ZP37 | Cell lines | |
| Derived from it | C5ROLas | CVCL_ZP36 | Cell lines |
Cell banks0
None in this release.
Data dates
The date of each source this release read.
Sources 4
- CellosaurusCC BY 4.0, with credit to Cellosaurus (SIB)
- PubMed Central's articlesTitles shown only for CC0, CC BY and public domain articles
- NLM's PMC Article DatasetsCourtesy of NLM, which does not endorse this database
- PubMedNLM's terms
Each source's terms
- CellosaurusCC BY 4.0. Cellosaurus's README: "we have chosen to apply the Creative Commons Attribution 4.0 International (CC BY 4.0) license to Cellosaurus (https://creativecommons.org/licenses/by/4.0/). This means that you are free to copy and redistribute Cellosaurus in any medium or format. You can remix, transform, and build upon Cellosaurus for any purpose, even commercially. You must give appropriate credit, provide a link to the license, and indicate if changes were made." Copyright (c) CALIPHO group, SIB Swiss Institute of Bioinformatics. Read on 14 Nov 2026 at https://ftp.expasy.org/databases/cellosaurus/README
- PubMed Central's articlesEach article's own license. Its words show only under CC0, CC BY or public domain
- NLM's PMC Article DatasetsNLM's PMC Article Datasets on AWS, https://registry.opendata.aws/ncbi-pmc. Its terms: users "acknowledge NLM as the source of the data in a clear and conspicuous manner", do not use the PubMed Central wordmark or the PMC logo, do not "indicate or imply that NLM/NIH/HHS has endorsed" a product, and "only distribute data that are licensed for redistribution". Each article keeps its own license: https://pmc.ncbi.nlm.nih.gov/about/copyright/
- PubMedNLM's terms
Cellosaurus, SIB Swiss Institute of Bioinformatics, https://www.cellosaurus.org, CC BY 4.0. Its problem notes are given in its own words.
For software
Read this cell line from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/cell-lines/v1/CVCL_ZP35
GET https://conductscience.org/api/cell-lines/v1/CVCL_ZP35/problems