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95,747 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
GM27160
 
Resource Report
Resource Website
RRID:CVCL_VH43 Homo sapiens (Human) Population: Indian. Finite cell line Female Coriell:GM27160,
Wikidata:Q54854146
CVCL_VH43 2026-07-25 04:38:00 0
GM27172
 
Resource Report
Resource Website
RRID:CVCL_UF17 Homo sapiens (Human) CADASIL syndrome Population: Caucasian. Transformed cell line Female Coriell:GM27172,
Wikidata:Q93933053
CVCL_UF17 2026-07-25 04:38:00 0
GM26580
 
Resource Report
Resource Website
RRID:CVCL_VI95 Homo sapiens (Human) Pitt-Hopkins syndrome Population: Caucasian and Native North American. Finite cell line Female Coriell:GM26580,
Wikidata:Q93932688
CVCL_VI95 2026-07-25 04:37:59 0
GM27123
 
Resource Report
Resource Website
RRID:CVCL_A2PX Homo sapiens (Human) Bethlem myopathy 1 Population: Caucasian; Swiss. Transformed cell line Female Coriell:GM27123,
Wikidata:Q105507089
CVCL_A2PX 2026-07-25 04:38:00 0
GM26643
 
Resource Report
Resource Website
Coriell Cat# GM26643, RRID:CVCL_A2WL Homo sapiens (Human) Ehlers-Danlos syndrome, type I Transformed cell line Female Coriell GM26643 Coriell:GM26643,
Wikidata:Q105507085
CVCL_A2WL 2026-07-25 04:38:00 0
GM26259
 
Resource Report
Resource Website
Coriell Cat# GM26259, RRID:CVCL_YP71 Homo sapiens (Human) Population: Caucasian and Native North American. Transformed cell line Female Coriell GM26259 Coriell:GM26259,
Wikidata:Q93932640
CVCL_YP71 2026-07-25 04:37:59 0
GM27134
 
Resource Report
Resource Website
Coriell Cat# GM27134, RRID:CVCL_YN21 Homo sapiens (Human) Population: Caucasian; English/German/Italian. Transformed cell line Female Coriell GM27134 Coriell:GM27134,
Wikidata:Q93933021
CVCL_YN21 2026-07-25 04:38:00 0
GM27162
 
Resource Report
Resource Website
RRID:CVCL_VH44 Homo sapiens (Human) Mucopolysaccharidosis type IIIA Population: Caucasian. Induced pluripotent stem cell Female GM27162*B Coriell:GM27162,
Wikidata:Q54854147
cvcl_0m06 CVCL_VH44 2026-07-25 04:38:00 0
GM27105
 
Resource Report
Resource Website
RRID:CVCL_WP06 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female Coriell:GM27105,
Wikidata:Q93933005
CVCL_WP06 2026-07-25 04:38:00 0
GM27141
 
Resource Report
Resource Website
Coriell Cat# GM27141, RRID:CVCL_YN27 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female Coriell GM27141 Coriell:GM27141,
Wikidata:Q93933031
CVCL_YN27 2026-07-25 04:38:00 0
GM26251
 
Resource Report
Resource Website
RRID:CVCL_LH32 Homo sapiens (Human) Population: Jewish; Ashkenazi. Transformed cell line Female Coriell:GM26251,
Wikidata:Q54854097
CVCL_LH32 2026-07-25 04:37:59 0
GM27205
 
Resource Report
Resource Website
RRID:CVCL_YN31 Homo sapiens (Human) Population: Caucasian; Dutch. Transformed cell line Female Coriell:GM27205,
Wikidata:Q93933078
CVCL_YN31 2026-07-25 04:38:01 0
GM27336
 
Resource Report
Resource Website
RRID:CVCL_XC51 Homo sapiens (Human) Transformed cell line Female Coriell:GM27336,
Wikidata:Q93933169
CVCL_XC51 2026-07-25 04:38:02 0
GM27250
 
Resource Report
Resource Website
RRID:CVCL_VV58 Homo sapiens (Human) Population: Caucasian; French and Chinese. Transformed cell line Female Coriell:GM27250,
Wikidata:Q93933125
CVCL_VV58 2026-07-25 04:38:01 0
GM27326
 
Resource Report
Resource Website
Coriell Cat# GM27326, RRID:CVCL_YN41 Homo sapiens (Human) Transformed cell line Female Coriell GM27326 Coriell:GM27326,
Wikidata:Q93933161
CVCL_YN41 2026-07-25 04:38:02 0
GM27206
 
Resource Report
Resource Website
RRID:CVCL_YN32 Homo sapiens (Human) Population: Caucasian; Dutch. Finite cell line Female Coriell:GM27206,
Wikidata:Q93933081
CVCL_YN32 2026-07-25 04:38:01 0
GM27288
 
Resource Report
Resource Website
RRID:CVCL_YN37 Homo sapiens (Human) Developmental and epileptic encephalopathy 25 Population: Caucasian. Transformed cell line Female Coriell:GM27288,
Wikidata:Q93933148
CVCL_YN37 2026-07-25 04:38:01 0
GM27267
 
Resource Report
Resource Website
RRID:CVCL_VV61 Homo sapiens (Human) Rett syndrome, congenital variant Transformed cell line Female Coriell:GM27267,
Wikidata:Q93933142
CVCL_VV61 2026-07-25 04:38:01 0
GM27315
 
Resource Report
Resource Website
RRID:CVCL_A1UJ Homo sapiens (Human) Rett syndrome, congenital variant Population: Southeast Asian; Thai and Chinese. Transformed cell line Female Coriell:GM27315,
Wikidata:Q105507125
CVCL_A1UJ 2026-07-25 04:38:01 0
GM27327
 
Resource Report
Resource Website
RRID:CVCL_VV71 Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 Induced pluripotent stem cell Female GM27327*B Coriell:GM27327,
Wikidata:Q93933163
cvcl_ln47 CVCL_VV71 2026-07-25 04:38:02 0

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