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95,747 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
GM24513
 
Resource Report
Resource Website
RRID:CVCL_AZ33 Homo sapiens (Human) Transformed cell line Female Coriell:GM24513,
Wikidata:Q54853772
CVCL_AZ33 2026-09-05 10:59:51 0
GM24601
 
Resource Report
Resource Website
Coriell Cat# GM24601, RRID:CVCL_1C83 Homo sapiens (Human) Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. PMID:27724973
PMID:37751688
Transformed cell line Female Coriell GM24601 Coriell:GM24601,
Wikidata:Q54853799
CVCL_1C83 2026-09-05 10:59:52 0
GM24559
 
Resource Report
Resource Website
RRID:CVCL_Y801 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian. Induced pluripotent stem cell Female GM24559*B Coriell:GM24559,
SKIP:SKIP000705,
Wikidata:Q54853784
cvcl_y794 CVCL_Y801 2026-09-05 10:59:51 0
GM24465
 
Resource Report
Resource Website
Coriell Cat# GM24465, RRID:CVCL_5T39 Homo sapiens (Human) Transformed cell line Female Coriell GM24465 Coriell:GM24465,
Wikidata:Q54853761
CVCL_5T39 2026-09-05 10:59:51 0
GM24511
 
Resource Report
Resource Website
RRID:CVCL_AZ32 Homo sapiens (Human) Attention deficit hyperactivity disorder Transformed cell line Female Coriell:GM24511,
Wikidata:Q54853771
CVCL_AZ32 2026-09-05 10:59:51 0
GM24527
 
Resource Report
Resource Website
RRID:CVCL_5K70 Homo sapiens (Human) Smith-Magenis syndrome Transformed cell line Female Coriell:GM24527,
Wikidata:Q54853778
CVCL_5K70 2026-09-05 10:59:51 0
GM24599
 
Resource Report
Resource Website
Coriell Cat# GM24599, RRID:CVCL_1C82 Homo sapiens (Human) Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. PMID:27724973
PMID:37751688
Transformed cell line Female Coriell GM24599 Coriell:GM24599,
Wikidata:Q54853798
CVCL_1C82 2026-09-05 10:59:52 0
GM24467
 
Resource Report
Resource Website
RRID:CVCL_AZ55 Homo sapiens (Human) Rigid spine muscular dystrophy 1 Finite cell line Female Coriell:GM24467,
Wikidata:Q54853762
CVCL_AZ55 2026-09-05 10:59:51 0
GM24513
 
Resource Report
Resource Website
Coriell Cat# GM24513, RRID:CVCL_AZ33 Homo sapiens (Human) Transformed cell line Female Coriell GM24513 Coriell:GM24513,
Wikidata:Q54853772
CVCL_AZ33 2026-09-05 10:59:51 0
GM24581
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM24581, RRID:CVCL_1N90 Homo sapiens (Human) Population: Caucasian. Induced pluripotent stem cell Female GM24581*B Coriell GM24581 Coriell:GM24581,
SKIP:SKIP000664,
Wikidata:Q54853785
cvcl_7348 CVCL_1N90 2026-09-05 10:59:51 0
GM24406
 
Resource Report
Resource Website
RRID:CVCL_AZ54 Homo sapiens (Human) Bethlem myopathy 1 Finite cell line Female Coriell:GM24406,
Wikidata:Q54853753
CVCL_AZ54 2026-09-05 10:59:51 0
GM24366
 
Resource Report
Resource Website
Coriell Cat# GM24366, RRID:CVCL_AZ26 Homo sapiens (Human) Transformed cell line Female Coriell GM24366 Coriell:GM24366,
Wikidata:Q54853738
CVCL_AZ26 2026-09-05 10:59:50 0
GM24406
 
Resource Report
Resource Website
Coriell Cat# GM24406, RRID:CVCL_AZ54 Homo sapiens (Human) Bethlem myopathy 1 Finite cell line Female Coriell GM24406 Coriell:GM24406,
Wikidata:Q54853753
CVCL_AZ54 2026-09-05 10:59:51 0
GM24592
 
Resource Report
Resource Website
Coriell Cat# GM24592, RRID:CVCL_HL24 Homo sapiens (Human) Turner syndrome Transformed cell line Female Coriell GM24592 Coriell:GM24592,
Wikidata:Q54853793
CVCL_HL24 2026-09-05 10:59:51 0
GM24392
 
Resource Report
Resource Website
Coriell Cat# GM24392, RRID:CVCL_AD87 Homo sapiens (Human) X-linked centronuclear myopathy Population: Lebanese. Transformed cell line Female Coriell GM24392 Coriell:GM24392,
Wikidata:Q54853749
CVCL_AD87 2026-09-05 10:59:50 0
GM24603
 
Resource Report
Resource Website
Coriell Cat# GM24603, RRID:CVCL_1C85 Homo sapiens (Human) Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. PMID:27724973
PMID:37751688
Transformed cell line Female Coriell GM24603 Coriell:GM24603,
Wikidata:Q54853801
CVCL_1C85 2026-09-05 10:59:52 0
GM24465
 
Resource Report
Resource Website
RRID:CVCL_5T39 Homo sapiens (Human) Transformed cell line Female Coriell:GM24465,
Wikidata:Q54853761
CVCL_5T39 2026-09-05 10:59:51 0
GM24586
 
Resource Report
Resource Website
Coriell Cat# GM24586, RRID:CVCL_5T41 Homo sapiens (Human) Finite cell line Female Coriell GM24586 Coriell:GM24586,
Wikidata:Q54853787
CVCL_5T41 2026-09-05 10:59:51 0
GM24593
 
Resource Report
Resource Website
RRID:CVCL_AZ41 Homo sapiens (Human) Turner syndrome Population: Bangladeshi. Transformed cell line Female Coriell:GM24593,
Wikidata:Q54853794
CVCL_AZ41 2026-09-05 10:59:51 0
GM24603
 
Resource Report
Resource Website
RRID:CVCL_1C85 Homo sapiens (Human) Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. PMID:27724973
PMID:37751688
Transformed cell line Female Coriell:GM24603,
Wikidata:Q54853801
CVCL_1C85 2026-09-05 10:59:52 0

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