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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
GM12158
 
Resource Report
Resource Website
RRID:CVCL_0P70 Homo sapiens (Human) Hepatolenticular degeneration Population: Caucasian. Finite cell line Female CLO:CLO_0019139,
Coriell:GM12158,
Wikidata:Q54845584
CVCL_0P70 2026-08-01 05:06:42 0
GM12218
 
Resource Report
Resource Website
Coriell Cat# GM12218, RRID:CVCL_5P64 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell GM12218 Coriell:GM12218,
Wikidata:Q54845596
CVCL_5P64 2026-08-01 05:06:39 0
GM12139
 
Resource Report
Resource Website
RRID:CVCL_5D06 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. PMID:20856902
PMID:24924344
Transformed cell line Female CLO:CLO_0019126,
Coriell:GM12139,
GEO:GSM420789,
Wikidata:Q54845557
CVCL_5D06 2026-08-01 05:06:39 0
GM12136
 
Resource Report
Resource Website
RRID:CVCL_N194 Homo sapiens (Human) Population: Caucasian; Northern European., Part of: Human variation panel. PMID:1333075 Transformed cell line Female GM17006 CLO:CLO_0018055,
CLO:CLO_0019104,
Coriell:GM12136,
Coriell:GM17006,
Wikidata:Q54845554
CVCL_N194 2026-08-01 05:06:38 0
GM12150
 
Resource Report
Resource Website
RRID:CVCL_5D13 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:15514893
PMID:20856902
PMID:24924344
Transformed cell line Female CEPH-1408-NA12150, 1408-1022 CLO:CLO_0019147,
Coriell:GM12150,
dbMHC:48675,
GEO:GSM25557,
GEO:GSM30120,
GEO:GSM316243,
GEO:GSM316244,
GEO:GSM316245,
GEO:GSM420802,
IHW:IHW01150,
IPD-IMGT/HLA:25945,
Wikidata:Q54845575
CVCL_5D13 2026-08-01 05:06:38 0
GM12132
 
Resource Report
Resource Website
Coriell Cat# GM12132, RRID:CVCL_5J58 Homo sapiens (Human) Transformed cell line Female Coriell GM12132 CLO:CLO_0019101,
Coriell:GM12132,
Wikidata:Q54845549
CVCL_5J58 2026-08-01 05:06:38 0
GM12135
 
Resource Report
Resource Website
RRID:CVCL_U536 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0019105,
Coriell:GM12135,
Wikidata:Q54845553
CVCL_U536 2026-08-01 05:06:41 0
GM12135
 
Resource Report
Resource Website
Coriell Cat# GM12135, RRID:CVCL_U536 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell GM12135 CLO:CLO_0019105,
Coriell:GM12135,
Wikidata:Q54845553
CVCL_U536 2026-08-01 05:06:38 0
GM12201
 
Resource Report
Resource Website
RRID:CVCL_5M52 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female CLO:CLO_0019163,
Coriell:GM12201,
Wikidata:Q54845589
CVCL_5M52 2026-08-01 05:06:40 0
GM12147
 
Resource Report
Resource Website
RRID:CVCL_5D10 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:15514893
PMID:20856902
PMID:24924344
Transformed cell line Female CEPH-1408-NA12147, 1408-1011 CLO:CLO_0019120,
Coriell:GM12147,
dbMHC:48672,
GEO:GSM25554,
GEO:GSM30117,
GEO:GSM316237,
GEO:GSM316238,
GEO:GSM316239,
GEO:GSM420799,
IHW:IHW01140,
IPD-IMGT/HLA:25937,
Wikidata:Q54845572
CVCL_5D10 2026-08-01 05:06:38 0
GM12147
 
Resource Report
Resource Website
Coriell Cat# GM12147, RRID:CVCL_5D10 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:15514893
PMID:20856902
PMID:24924344
Transformed cell line Female CEPH-1408-NA12147, 1408-1011 Coriell GM12147 CLO:CLO_0019120,
Coriell:GM12147,
dbMHC:48672,
GEO:GSM25554,
GEO:GSM30117,
GEO:GSM316237,
GEO:GSM316238,
GEO:GSM316239,
GEO:GSM420799,
IHW:IHW01140,
IPD-IMGT/HLA:25937,
Wikidata:Q54845572
CVCL_5D10 2026-08-01 05:06:42 0
GM12199
 
Resource Report
Resource Website
Coriell Cat# GM12199, RRID:CVCL_0P72 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female Coriell GM12199 CLO:CLO_0019161,
Coriell:GM12199,
Wikidata:Q54845587
CVCL_0P72 2026-08-01 05:06:40 0
GM12225
 
Resource Report
Resource Website
RRID:CVCL_V423 Homo sapiens (Human) Incontinentia pigmenti Population: Caucasian. Transformed cell line Female CLO:CLO_0019183,
Coriell:GM12225,
Wikidata:Q54845602
CVCL_V423 2026-08-01 05:06:40 0
GM12227
 
Resource Report
Resource Website
Coriell Cat# GM12227, RRID:CVCL_5J60 Homo sapiens (Human) Transformed cell line Female Coriell GM12227 CLO:CLO_0019189,
Coriell:GM12227,
Wikidata:Q54845604
CVCL_5J60 2026-08-01 05:06:42 0
GM12127
 
Resource Report
Resource Website
RRID:CVCL_GR16 Homo sapiens (Human) Cirrhosis Transformed cell line Female CLO:CLO_0019107,
Coriell:GM12127,
Wikidata:Q54845546
CVCL_GR16 2026-08-01 05:06:41 0
GM12226
 
Resource Report
Resource Website
Coriell Cat# GM12226, RRID:CVCL_V424 Homo sapiens (Human) Incontinentia pigmenti Population: Caucasian. Transformed cell line Female Coriell GM12226 CLO:CLO_0019187,
Coriell:GM12226,
Wikidata:Q54845603
CVCL_V424 2026-08-01 05:06:40 0
GM12220
 
Resource Report
Resource Website
Coriell Cat# GM12220, RRID:CVCL_DB81 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female Coriell GM12220 CLO:CLO_0019179,
Coriell:GM12220,
Wikidata:Q54845597
CVCL_DB81 2026-08-01 05:06:40 0
GM12158
 
Resource Report
Resource Website
Coriell Cat# GM12158, RRID:CVCL_0P70 Homo sapiens (Human) Hepatolenticular degeneration Population: Caucasian. Finite cell line Female Coriell GM12158 CLO:CLO_0019139,
Coriell:GM12158,
Wikidata:Q54845584
CVCL_0P70 2026-08-01 05:06:39 0
GM12203
 
Resource Report
Resource Website
RRID:CVCL_5M54 Homo sapiens (Human) Proteus syndrome Population: Caucasian. Transformed cell line Female CLO:CLO_0019166,
Coriell:GM12203,
Wikidata:Q54845591
CVCL_5M54 2026-08-01 05:06:39 0
GM12222
 
Resource Report
Resource Website
Coriell Cat# GM12222, RRID:CVCL_AY62 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female Coriell GM12222 CLO:CLO_0019184,
Coriell:GM12222,
Wikidata:Q54845599
CVCL_AY62 2026-08-01 05:06:39 0

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