Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

Preparing word cloud

×

Suggested Search Criteria

Enter extra filters to help narrow your search

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Current Facets and Filters

  • Issues Status:issues found (facet)

Facets


Recent searches

Snippet view Table view
Click the to add this resource to an Authentication Report or Collection

19,458 Results - per page

Show More Columns | Download Top 1000 Results

Name Proper Citation Organism Disease Comments Defining Citation Category Sex Synonyms Vendor Catalog Number Cross References Hierarchy Originate from Same Individual ID Record Last Update Mentions Count
ND29509
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_T860 Homo sapiens (Human) Amyotrophic lateral sclerosis 1 Population: Caucasian. PMID:22952635 Finite cell line Male Coriell:ND29509,
NHCDR:ND29509,
Wikidata:Q54929234
CVCL_T860 2026-07-25 04:56:39 0
ND29510
 
Resource Report
Resource Website
1+ mentions
Discontinued
RRID:CVCL_Y813 Homo sapiens (Human) PMID:22952635 Finite cell line Female Coriell:ND29510,
NHCDR:ND29510,
Wikidata:Q54929235
CVCL_Y813 2026-07-25 04:56:39 1
ND29523
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY51 Homo sapiens (Human) Amyotrophic lateral sclerosis 1 PMID:22952635 Finite cell line Male Coriell:ND29523,
NHCDR:ND29523,
Wikidata:Q54929237
CVCL_EY51 2026-07-25 04:56:39 0
ND29802
 
Resource Report
Resource Website
1+ mentions
Discontinued
RRID:CVCL_DD50 Homo sapiens (Human) Parkinson disease 8, autosomal dominant Population: Caucasian. PMID:22952635
PMID:27191603
Finite cell line Male BioSample:SAMN00805493,
Coriell:ND29802,
NHCDR:ND29802,
Wikidata:Q54929281
CVCL_DD50 2026-07-25 04:56:40 1
ND29563
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_Y894 Homo sapiens (Human) Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia Population: Caucasian. Finite cell line Male Coriell:ND29563,
NHCDR:ND29563,
Wikidata:Q54929256
CVCL_Y894 2026-07-25 04:56:39 0
ND29492
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_DD51 Homo sapiens (Human) Parkinson disease 8, autosomal dominant PMID:22952635
PMID:27191603
Finite cell line Male Coriell:ND29492,
NHCDR:ND29492,
Wikidata:Q54929232
CVCL_DD51 2026-07-25 04:56:39 0
ND29689
 
Resource Report
Resource Website
Discontinued
Coriell Cat# ND29689, RRID:CVCL_EY53 Homo sapiens (Human) Amyotrophic lateral sclerosis Population: Caucasian. Finite cell line Male Coriell ND29689 Coriell:ND29689,
NHCDR:ND29689,
Wikidata:Q54929270
CVCL_EY53 2026-07-25 04:56:39 0
ND29510
 
Resource Report
Resource Website
1+ mentions
Discontinued
NHCDR Cat# ND29510, RRID:CVCL_Y813 Homo sapiens (Human) PMID:22952635 Finite cell line Female NHCDR ND29510 Coriell:ND29510,
NHCDR:ND29510,
Wikidata:Q54929235
CVCL_Y813 2026-07-25 04:56:39 1
ND29970
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY57 Homo sapiens (Human) Huntington's disease PMID:22952635 Finite cell line Male Coriell:ND29970,
NHCDR:ND29970,
Wikidata:Q54929298
CVCL_EY57 2026-07-25 04:56:40 0
ND30016
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY60 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington's disease but at risk for disease (HTT has CAG repeat length greater than or equal to 36). PMID:22952635 Finite cell line Female Coriell:ND30016,
NHCDR:ND30016,
Wikidata:Q54929314
CVCL_EY60 2026-07-25 04:56:40 0
ND29971
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY58 Homo sapiens (Human) PMID:22952635 Finite cell line Female Coriell:ND29971,
NHCDR:ND29971,
Wikidata:Q54929306
CVCL_EY58 2026-07-25 04:56:40 0
ND30259
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY65 Homo sapiens (Human) Huntington's disease PMID:22952635 Finite cell line Female Coriell:ND30259,
NHCDR:ND30259,
Wikidata:Q54929341
CVCL_EY65 2026-07-25 04:56:41 0
ND29971
 
Resource Report
Resource Website
Discontinued
Coriell Cat# ND29971, RRID:CVCL_EY58 Homo sapiens (Human) PMID:22952635 Finite cell line Female Coriell ND29971 Coriell:ND29971,
NHCDR:ND29971,
Wikidata:Q54929306
CVCL_EY58 2026-07-25 04:56:40 0
ND30014
 
Resource Report
Resource Website
Discontinued
NHCDR Cat# ND30014, RRID:CVCL_Y898 Homo sapiens (Human) PMID:22952635
PMID:30256717
Finite cell line Female NHCDR ND30014 Coriell:ND30014,
NHCDR:ND30014,
Wikidata:Q54929312
CVCL_Y898 2026-07-25 04:56:40 0
ND30047
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY61 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington's disease but at risk for disease (HTT has CAG repeat length greater than or equal to 36). PMID:22952635 Finite cell line Female Coriell:ND30047,
NHCDR:ND30047,
Wikidata:Q54929315
CVCL_EY61 2026-07-25 04:56:40 0
ND30015
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY59 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington's disease but at risk for disease (HTT has CAG repeat length greater than or equal to 36). PMID:22952635 Finite cell line Female Coriell:ND30015,
NHCDR:ND30015,
Wikidata:Q54929313
CVCL_EY59 2026-07-25 04:56:40 0
ND29968
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY55 Homo sapiens (Human) Parkinson disease 2, autosomal recessive juvenile PMID:22952635 Finite cell line Male BioSample:SAMN00805499,
Coriell:ND29968,
NHCDR:ND29968,
Wikidata:Q54929295
CVCL_EY55 2026-07-25 04:56:40 0
ND30260
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY66 Homo sapiens (Human) Huntington's disease PMID:22952635 Finite cell line Female Coriell:ND30260,
NHCDR:ND30260,
Wikidata:Q54929342
CVCL_EY66 2026-07-25 04:56:41 0
ND29969
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY56 Homo sapiens (Human) Parkinson disease 2, autosomal recessive juvenile PMID:22952635 Finite cell line Female BioSample:SAMN00805501,
Coriell:ND29969,
NHCDR:ND29969,
Wikidata:Q54929296
CVCL_EY56 2026-07-25 04:56:40 0
ND30159
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY63 Homo sapiens (Human) Parkinson disease PMID:22952635 Finite cell line Female BioSample:SAMN00805543,
Coriell:ND30159,
NHCDR:ND30159,
Wikidata:Q54929326
CVCL_EY63 2026-07-25 04:56:40 0

Can't find your Cell Line?

We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. If you want to find a specific cell line, it's easier to enter an RRID or add the vendor information to search. You can refine the search results using Facets on the left side of the search results page. If you are on the table view, you can also search in a specific column by clicking the column title and enter the keywords.

If you still could not find your cell line in the search results, please help us by registering it into the system — it's easy. Register it with the Cellosaurus. An RRID will be generated in 1-2 business days.

Can't find the RRID you're searching for? X
X
  1. RRID Portal Resources

    Welcome to the RRID Resources search. From here you can search through a compilation of resources used by RRID and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that RRID has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on RRID then you can log in from here to get additional features in RRID such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Collections

    If you are logged into RRID you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  6. Facets

    Here are the facets that you can filter the data by.

  7. Further Questions

    If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.