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  • References:pmid:23665875 (facet)

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1,669 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
GM07873
 
Resource Report
Resource Website
Coriell Cat# GM07873, RRID:CVCL_5N71 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Male Coriell GM07873 CLO:CLO_0010307,
Coriell:GM07873,
Wikidata:Q54842977
CVCL_5N71 2026-09-05 10:55:47 0
GM07895
 
Resource Report
Resource Website
RRID:CVCL_N073 Homo sapiens (Human) Population: Indo Pakistani., Part of: Human variation panel. PMID:23665875 Transformed cell line Female GM17024, GM 7895, GM7895 CLO:CLO_0010317,
CLO:CLO_0014704,
Coriell:GM07895,
Coriell:GM17024,
Wikidata:Q54842990
CVCL_N073 2026-09-05 10:55:48 0
GM07895
 
Resource Report
Resource Website
Coriell Cat# GM07895, RRID:CVCL_N073 Homo sapiens (Human) Population: Indo Pakistani., Part of: Human variation panel. PMID:23665875 Transformed cell line Female GM17024, GM 7895, GM7895 Coriell GM07895 CLO:CLO_0010317,
CLO:CLO_0014704,
Coriell:GM07895,
Coriell:GM17024,
Wikidata:Q54842990
CVCL_N073 2026-09-05 10:55:48 0
GM07945
 
Resource Report
Resource Website
Coriell Cat# GM07945, RRID:CVCL_5N73 Homo sapiens (Human) Adenosine deaminase deficiency PMID:23665875 Transformed cell line Male Coriell GM07945 CLO:CLO_0010323,
Coriell:GM07945,
Wikidata:Q54843007
CVCL_5N73 2026-09-05 10:55:48 0
GM07945
 
Resource Report
Resource Website
RRID:CVCL_5N73 Homo sapiens (Human) Adenosine deaminase deficiency PMID:23665875 Transformed cell line Male CLO:CLO_0010323,
Coriell:GM07945,
Wikidata:Q54843007
CVCL_5N73 2026-09-05 10:55:48 0
GM07965
 
Resource Report
Resource Website
Coriell Cat# GM07965, RRID:CVCL_1Q38 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM07965 CLO:CLO_0010334,
Coriell:GM07965,
Wikidata:Q54843012
CVCL_1Q38 2026-09-05 10:55:48 0
GM07994
 
Resource Report
Resource Website
RRID:CVCL_2T44 Homo sapiens (Human) PMID:23665875 Finite cell line Male CLO:CLO_0010043,
Coriell:GM07994,
Wikidata:Q54843039
CVCL_2T44 2026-09-05 10:55:49 0
GM07995
 
Resource Report
Resource Website
Coriell Cat# GM07995, RRID:CVCL_5N78 Homo sapiens (Human) Trisomy 9 Population: Caucasian. PMID:23665875 Finite cell line Male Coriell GM07995 CLO:CLO_0010040,
Coriell:GM07995,
Wikidata:Q54843040
CVCL_5N78 2026-09-05 10:55:49 0
GM07939
 
Resource Report
Resource Website
Coriell Cat# GM07939, RRID:CVCL_5N72 Homo sapiens (Human) 22q11.2 deletion syndrome PMID:23665875 Transformed cell line Male Coriell GM07939 CLO:CLO_0010326,
Coriell:GM07939,
Wikidata:Q54843002
CVCL_5N72 2026-09-05 10:55:48 0
GM07891
 
Resource Report
Resource Website
Coriell Cat# GM07891, RRID:CVCL_2T37 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Male Coriell GM07891 CLO:CLO_0010295,
Coriell:GM07891,
Wikidata:Q54842987
CVCL_2T37 2026-09-05 10:55:48 0
GM07890
 
Resource Report
Resource Website
Coriell Cat# GM07890, RRID:CVCL_V283 Homo sapiens (Human) PMID:23665875 Transformed cell line Female GM 7890 Coriell GM07890 CLO:CLO_0010296,
Coriell:GM07890,
Wikidata:Q54842985
CVCL_V283 2026-09-05 10:55:48 0
GM07987
 
Resource Report
Resource Website
RRID:CVCL_2T43 Homo sapiens (Human) PMID:23665875 Finite cell line Male CLO:CLO_0010049,
Coriell:GM07987,
Wikidata:Q54843035
CVCL_2T43 2026-09-05 10:55:49 0
GM07994
 
Resource Report
Resource Website
Coriell Cat# GM07994, RRID:CVCL_2T44 Homo sapiens (Human) PMID:23665875 Finite cell line Male Coriell GM07994 CLO:CLO_0010043,
Coriell:GM07994,
Wikidata:Q54843039
CVCL_2T44 2026-09-05 10:55:49 0
GM07895
 
Resource Report
Resource Website
Coriell Cat# GM17024, RRID:CVCL_N073 Homo sapiens (Human) Population: Indo Pakistani., Part of: Human variation panel. PMID:23665875 Transformed cell line Female GM17024, GM 7895, GM7895 Coriell GM17024 CLO:CLO_0010317,
CLO:CLO_0014704,
Coriell:GM07895,
Coriell:GM17024,
Wikidata:Q54842990
CVCL_N073 2026-09-05 10:55:48 0
GM07873
 
Resource Report
Resource Website
RRID:CVCL_5N71 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Male CLO:CLO_0010307,
Coriell:GM07873,
Wikidata:Q54842977
CVCL_5N71 2026-09-05 10:55:47 0
GM07985
 
Resource Report
Resource Website
Coriell Cat# GM07985, RRID:CVCL_5N76 Homo sapiens (Human) Holoprosencephaly Population: African American. PMID:23665875 Finite cell line Female Coriell GM07985 CLO:CLO_0010003,
Coriell:GM07985,
Wikidata:Q54843028
CVCL_5N76 2026-09-05 10:55:49 0
GM08014
 
Resource Report
Resource Website
RRID:CVCL_5M40 Homo sapiens (Human) Hereditary spherocytosis PMID:23665875 Transformed cell line Female CLO:CLO_0010037,
Coriell:GM08014,
Wikidata:Q54843048
CVCL_5M40 2026-09-05 10:55:49 0
GM08123
 
Resource Report
Resource Website
RRID:CVCL_2T49 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Male CLO:CLO_0010108,
Coriell:GM08123,
Wikidata:Q54843088
CVCL_2T49 2026-09-05 10:55:50 0
GM08146
 
Resource Report
Resource Website
RRID:CVCL_5N82 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0010106,
Coriell:GM08146,
Wikidata:Q54843092
CVCL_5N82 2026-09-05 10:55:50 0
GM08009
 
Resource Report
Resource Website
Coriell Cat# GM08009, RRID:CVCL_2T45 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM08009 CLO:CLO_0010047,
Coriell:GM08009,
Wikidata:Q54843044
CVCL_2T45 2026-09-05 10:55:49 0

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