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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
GM11602
 
Resource Report
Resource Website
RRID:CVCL_AA02 Homo sapiens (Human) Neurofibromatosis type 1 PMID:8268926 Transformed cell line Female CLO:CLO_0021199,
Coriell:GM11602,
Wikidata:Q54845184
CVCL_AA02 2026-08-15 04:31:24 0
GM11675
 
Resource Report
Resource Website
RRID:CVCL_4E09 Homo sapiens (Human) Transformed cell line Male CLO:CLO_0021335,
Coriell:GM11675,
Wikidata:Q54845215
CVCL_4E09 2026-08-15 04:31:24 0
GM11570
 
Resource Report
Resource Website
RRID:CVCL_5P58 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0021051,
Coriell:GM11570,
Wikidata:Q54845159
CVCL_5P58 2026-08-15 04:31:23 0
GM11627
 
Resource Report
Resource Website
Coriell Cat# GM11627, RRID:CVCL_AJ79 Homo sapiens (Human) Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Female Coriell GM11627 CLO:CLO_0021358,
Coriell:GM11627,
Wikidata:Q54845199
CVCL_AJ79 2026-08-15 04:31:24 0
GM11579
 
Resource Report
Resource Website
Coriell Cat# GM11579, RRID:CVCL_AJ68 Homo sapiens (Human) Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Female Coriell GM11579 CLO:CLO_0021220,
Coriell:GM11579,
Wikidata:Q54845165
CVCL_AJ68 2026-08-15 04:31:23 0
GM11611
 
Resource Report
Resource Website
RRID:CVCL_AJ75 Homo sapiens (Human) Hepatocyte nuclear factor 4-alpha associated monogenic diabetes Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Male GM11611A CLO:CLO_0021182,
Coriell:GM11611,
Wikidata:Q54845189
CVCL_AJ75 2026-08-15 04:31:24 0
GM11686
 
Resource Report
Resource Website
RRID:CVCL_1S29 Homo sapiens (Human) Characteristics: Contains a neo-tagged human chromosome 2., Group: Human/rodent somatic cell hybrid. PMID:1438292 Hybrid cell line HA(2)A CLO:CLO_0021298,
Coriell:GM11686,
Wikidata:Q54845227
cvcl_3984 CVCL_1S29 2026-08-15 04:31:25 0
GM11692
 
Resource Report
Resource Website
RRID:CVCL_1S34 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. PMID:2045096 Hybrid cell line 1SHL3-14, 1SHL3 subclone 14 CLO:CLO_0021293,
Coriell:GM11692,
Wikidata:Q54845232
cvcl_1n51 CVCL_1S34 2026-08-15 04:31:25 0
GM11577
 
Resource Report
Resource Website
RRID:CVCL_AJ66 Homo sapiens (Human) Hepatocyte nuclear factor 4-alpha associated monogenic diabetes Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Female CLO:CLO_0021224,
Coriell:GM11577,
Wikidata:Q54845163
CVCL_AJ66 2026-08-15 04:31:23 0
GM11630
 
Resource Report
Resource Website
RRID:CVCL_AB12 Homo sapiens (Human) Multiple endocrine neoplasia type 1 Transformed cell line Male CLO:CLO_0021354,
Coriell:GM11630,
Wikidata:Q54845201
CVCL_AB12 2026-08-15 04:31:24 0
GM11707
 
Resource Report
Resource Website
Coriell Cat# GM11707, RRID:CVCL_1Y49 Homo sapiens (Human) Sandhoff disease Population: Caucasian. Finite cell line Male Coriell GM11707 CLO:CLO_0021257,
Coriell:GM11707,
Wikidata:Q54845235
CVCL_1Y49 2026-08-15 04:31:25 0
GM11601
 
Resource Report
Resource Website
RRID:CVCL_AA01 Homo sapiens (Human) Neurofibromatosis type 1 PMID:1719426 Transformed cell line Male CLO:CLO_0021200,
Coriell:GM11601,
Wikidata:Q54845182
CVCL_AA01 2026-08-15 04:31:24 0
GM11575
 
Resource Report
Resource Website
RRID:CVCL_1S26 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. Hybrid cell line X13-C9 CLO:CLO_0021226,
Coriell:GM11575,
Wikidata:Q54845161
CVCL_1S26 2026-08-15 04:31:23 0
GM11626
 
Resource Report
Resource Website
RRID:CVCL_AJ78 Homo sapiens (Human) Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Male CLO:CLO_0021350,
Coriell:GM11626,
Wikidata:Q54845198
CVCL_AJ78 2026-08-15 04:31:24 0
GM11677
 
Resource Report
Resource Website
Coriell Cat# GM11677, RRID:CVCL_DD86 Homo sapiens (Human) Osteogenesis imperfecta type II Population: Caucasian. Finite cell line Male Coriell GM11677 CLO:CLO_0021336,
Coriell:GM11677,
Wikidata:Q54845223
CVCL_DD86 2026-08-15 04:31:24 0
GM11597
 
Resource Report
Resource Website
RRID:CVCL_2U12 Homo sapiens (Human) Karyotypic information: 46,XX,der(9)(9qter->9p22::6q23->6qter) (Coriell=GM11597)., Population: Caucasian. Finite cell line Female CLO:CLO_0021204,
Coriell:GM11597,
Wikidata:Q54845178
CVCL_2U12 2026-08-15 04:31:23 0
GM11568
 
Resource Report
Resource Website
Coriell Cat# GM11568, RRID:CVCL_AJ64 Homo sapiens (Human) Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Male Coriell GM11568 CLO:CLO_0021049,
Coriell:GM11568,
Wikidata:Q54845157
CVCL_AJ64 2026-08-15 04:31:23 0
GM11571
 
Resource Report
Resource Website
RRID:CVCL_5P59 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0021052,
Coriell:GM11571,
Wikidata:Q54845160
CVCL_5P59 2026-08-15 04:31:23 0
GM11598
 
Resource Report
Resource Website
Coriell Cat# GM11598, RRID:CVCL_AJ71 Homo sapiens (Human) Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Female Coriell GM11598 CLO:CLO_0021203,
Coriell:GM11598,
Wikidata:Q54845179
CVCL_AJ71 2026-08-15 04:31:23 0
GM11597
 
Resource Report
Resource Website
Coriell Cat# GM11597, RRID:CVCL_2U12 Homo sapiens (Human) Karyotypic information: 46,XX,der(9)(9qter->9p22::6q23->6qter) (Coriell=GM11597)., Population: Caucasian. Finite cell line Female Coriell GM11597 CLO:CLO_0021204,
Coriell:GM11597,
Wikidata:Q54845178
CVCL_2U12 2026-08-15 04:31:23 0

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