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256,031 Results - per page

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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
GM12526
 
Resource Report
Resource Website
RRID:CVCL_5J67 Homo sapiens (Human) PMID:1746558 Transformed cell line Female CLO:CLO_0017886,
Coriell:GM12526,
Wikidata:Q54845831
CVCL_5J67 2026-09-12 05:34:34 0
GM12519
 
Resource Report
Resource Website
Coriell Cat# GM12519, RRID:CVCL_H549 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell GM12519 CLO:CLO_0017851,
Coriell:GM12519,
Wikidata:Q54845824
CVCL_H549 2026-09-12 05:34:33 0
GM12617
 
Resource Report
Resource Website
Coriell Cat# GM12617, RRID:CVCL_9X48 Homo sapiens (Human) Part of: CEPH/French pedigree cell line collection. PMID:24924344 Transformed cell line Male Coriell GM12617 CLO:CLO_0018064,
Coriell:GM12617,
Wikidata:Q54845901
CVCL_9X48 2026-09-12 05:34:35 0
GM12590
 
Resource Report
Resource Website
RRID:CVCL_5P65 Homo sapiens (Human) PMID:23665875 Finite cell line Male Coriell:GM12590,
Wikidata:Q54845883
CVCL_5P65 2026-09-12 05:34:35 0
GM12609
 
Resource Report
Resource Website
RRID:CVCL_V448 Homo sapiens (Human) Autosomal recessive polycystic kidney disease Finite cell line Female CLO:CLO_0018084,
Coriell:GM12609,
Wikidata:Q54845897
CVCL_V448 2026-09-12 05:34:35 0
GM12618
 
Resource Report
Resource Website
Coriell Cat# GM12618, RRID:CVCL_9Y64 Homo sapiens (Human) Part of: CEPH/French pedigree cell line collection. PMID:24924344 Transformed cell line Male Coriell GM12618 CLO:CLO_0018048,
Coriell:GM12618,
Wikidata:Q54845902
CVCL_9Y64 2026-09-12 05:34:35 0
GM12547
 
Resource Report
Resource Website
Coriell Cat# GM17008, RRID:CVCL_N196 Homo sapiens (Human) Population: Caucasian; Northern European., Part of: Human variation panel., Part of: CEPH/French pedigree cell line collection. Transformed cell line Male GM17008 Coriell GM17008 CLO:CLO_0017948,
CLO:CLO_0018052,
Coriell:GM12547,
Coriell:GM17008,
Wikidata:Q54845852
CVCL_N196 2026-09-12 05:34:34 0
GM12604
 
Resource Report
Resource Website
RRID:CVCL_Y706 Homo sapiens (Human) Ornithine carbamoyltransferase deficiency disease Population: Caucasian. Finite cell line Female CLO:CLO_0018077,
Coriell:GM12604,
Wikidata:Q54845894
CVCL_Y706 2026-09-12 05:34:35 0
GM12593
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7524 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. PMID:16260726 Transformed cell line Female GM17238 CLO:CLO_0014332,
CLO:CLO_0018080,
Coriell:GM12593,
Coriell:GM17238,
GEO:GSM569565,
GEO:GSM596302,
GEO:GSM596662,
GEO:GSM924840,
Wikidata:Q54845892
CVCL_7524 2026-09-12 05:34:35 1
GM12620
 
Resource Report
Resource Website
RRID:CVCL_9X51 Homo sapiens (Human) Part of: CEPH/French pedigree cell line collection. PMID:24924344 Transformed cell line Female CLO:CLO_0018050,
Coriell:GM12620,
Wikidata:Q54845904
CVCL_9X51 2026-09-12 05:34:35 0
GM12559
 
Resource Report
Resource Website
RRID:CVCL_9X32 Homo sapiens (Human) Part of: CEPH/French pedigree cell line collection. Transformed cell line Female CLO:CLO_0017762,
Coriell:GM12559,
Wikidata:Q54845866
CVCL_9X32 2026-09-12 05:34:34 0
GM12607
 
Resource Report
Resource Website
RRID:CVCL_V447 Homo sapiens (Human) Autosomal recessive polycystic kidney disease PMID:24009235 Finite cell line Female CLO:CLO_0018086,
Coriell:GM12607,
Wikidata:Q54845896
CVCL_V447 2026-09-12 05:34:35 0
GM12616
 
Resource Report
Resource Website
Coriell Cat# GM12616, RRID:CVCL_9X47 Homo sapiens (Human) Part of: CEPH/French pedigree cell line collection. PMID:24924344 Transformed cell line Female Coriell GM12616 CLO:CLO_0018061,
Coriell:GM12616,
Wikidata:Q54845900
CVCL_9X47 2026-09-12 05:34:35 0
GM12569
 
Resource Report
Resource Website
RRID:CVCL_9X42 Homo sapiens (Human) Part of: CEPH/French pedigree cell line collection. Transformed cell line Male CLO:CLO_0018109,
Coriell:GM12569,
GEO:GSM906187,
GEO:GSM906188,
Wikidata:Q54845876
CVCL_9X42 2026-09-12 05:34:35 0
GM12606
 
Resource Report
Resource Website
Coriell Cat# GM12606, RRID:CVCL_5P66 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM12606 CLO:CLO_0018088,
Coriell:GM12606,
Wikidata:Q54845895
CVCL_5P66 2026-09-12 05:34:35 0
GM12567
 
Resource Report
Resource Website
Coriell Cat# GM12567, RRID:CVCL_9X40 Homo sapiens (Human) Part of: CEPH/French pedigree cell line collection. Transformed cell line Male Coriell GM12567 CLO:CLO_0018118,
Coriell:GM12567,
Wikidata:Q54845874
CVCL_9X40 2026-09-12 05:34:35 0
GM12541
 
Resource Report
Resource Website
RRID:CVCL_5J80 Homo sapiens (Human) PMID:1746558 Transformed cell line Male CLO:CLO_0017906,
Coriell:GM12541,
Wikidata:Q54845848
CVCL_5J80 2026-09-12 05:34:34 0
GM12619
 
Resource Report
Resource Website
RRID:CVCL_9X50 Homo sapiens (Human) Part of: CEPH/French pedigree cell line collection. PMID:24924344 Transformed cell line Female CLO:CLO_0018047,
Coriell:GM12619,
Wikidata:Q54845903
CVCL_9X50 2026-09-12 05:34:35 0
GM12622
 
Resource Report
Resource Website
Coriell Cat# GM12622, RRID:CVCL_9X53 Homo sapiens (Human) Part of: CEPH/French pedigree cell line collection. PMID:24924344 Transformed cell line Female Coriell GM12622 CLO:CLO_0018054,
Coriell:GM12622,
Wikidata:Q54845906
CVCL_9X53 2026-09-12 05:34:35 0
GM12623
 
Resource Report
Resource Website
RRID:CVCL_9X54 Homo sapiens (Human) Part of: CEPH/French pedigree cell line collection. PMID:24924344 Transformed cell line Male CLO:CLO_0018051,
Coriell:GM12623,
Wikidata:Q54845907
CVCL_9X54 2026-09-12 05:34:35 0

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