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19,458 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
GM16286
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WC Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16286,
Wikidata:Q107115138
CVCL_A5WC 2026-07-25 04:35:56 0
GM16287
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WD Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Male Coriell:GM16287,
Wikidata:Q107115140
CVCL_A5WD 2026-07-25 04:35:56 0
GM16291
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WH Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16291,
Wikidata:Q107115150
CVCL_A5WH 2026-07-25 04:35:56 0
GM16295
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WL Homo sapiens (Human) PMID:28161093 Transformed cell line Male Coriell:GM16295,
Wikidata:Q107115158
CVCL_A5WL 2026-07-25 04:35:56 0
GM16333
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WM Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16333,
Wikidata:Q107115161
CVCL_A5WM 2026-07-25 04:35:57 0
GM16330
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM16330, RRID:CVCL_A5WR Homo sapiens (Human) PMID:28161093 Transformed cell line Sex unspecified Coriell GM16330 Coriell:GM16330,
Wikidata:Q107115159
CVCL_A5WR 2026-07-25 04:35:57 0
GM16436
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_0H58 Homo sapiens (Human) Tourette syndrome Transformed cell line Male JL281 Coriell:GM16436,
Wikidata:Q54848558
CVCL_0H58 2026-07-25 04:35:59 0
GM16434
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM16434, RRID:CVCL_0H57 Homo sapiens (Human) Transformed cell line Male JL203 Coriell GM16434 Coriell:GM16434,
Wikidata:Q54848556
CVCL_0H57 2026-07-25 04:35:59 0
GM16436
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM16436, RRID:CVCL_0H58 Homo sapiens (Human) Tourette syndrome Transformed cell line Male JL281 Coriell GM16436 Coriell:GM16436,
Wikidata:Q54848558
CVCL_0H58 2026-07-25 04:35:59 0
GM12059
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_4Z86 Homo sapiens (Human) X-linked ichthyosis Finite cell line Male CLO:CLO_0020646,
Coriell:GM12059,
Wikidata:Q54845494
CVCL_4Z86 2026-07-25 04:34:47 0
GM12269
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5D42 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. PMID:15514893 Transformed cell line Male CLO:CLO_0019427,
Coriell:GM12269,
GEO:GSM25592,
GEO:GSM30186,
Wikidata:Q54845648
CVCL_5D42 2026-07-25 04:34:51 0
GM12236
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM12236, RRID:CVCL_9611 Homo sapiens (Human) Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:17122850
PMID:19797678
PMID:20398888
PMID:20856902
PMID:21397061
PMID:26621101
PMID:29474986
Transformed cell line Female CEPH-1408-NA12236, 1408-1019 Coriell GM12236 CLO:CLO_0019202,
EFO:EFO_0001143,
Coriell:GM12236,
dbMHC:48683,
GEO:GSM25568,
GEO:GSM25569,
GEO:GSM112537,
GEO:GSM112842,
GEO:GSM273331,
GEO:GSM273332,
GEO:GSM314930,
GEO:GSM314931,
GEO:GSM420819,
GEO:GSM420820,
GEO:GSM486809,
GEO:GSM486810,
GEO:GSM648891,
GEO:GSM659966,
GEO:GSM660153,
GEO:GSM660360,
GEO:GSM905873,
GEO:GSM905968,
GEO:GSM906063,
IHW:IHW01148,
IPD-IMGT/HLA:25943,
Wikidata:Q54845620
CVCL_9611 2026-07-25 04:34:50 0
GM12236
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_9611 Homo sapiens (Human) Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:17122850
PMID:19797678
PMID:20398888
PMID:20856902
PMID:21397061
PMID:26621101
PMID:29474986
Transformed cell line Female CEPH-1408-NA12236, 1408-1019 CLO:CLO_0019202,
EFO:EFO_0001143,
Coriell:GM12236,
dbMHC:48683,
GEO:GSM25568,
GEO:GSM25569,
GEO:GSM112537,
GEO:GSM112842,
GEO:GSM273331,
GEO:GSM273332,
GEO:GSM314930,
GEO:GSM314931,
GEO:GSM420819,
GEO:GSM420820,
GEO:GSM486809,
GEO:GSM486810,
GEO:GSM648891,
GEO:GSM659966,
GEO:GSM660153,
GEO:GSM660360,
GEO:GSM905873,
GEO:GSM905968,
GEO:GSM906063,
IHW:IHW01148,
IPD-IMGT/HLA:25943,
Wikidata:Q54845620
CVCL_9611 2026-07-25 04:34:50 0
GM12408
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM12408, RRID:CVCL_5D91 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. Transformed cell line Male Coriell GM12408 CLO:CLO_0019806,
BioSample:SAMN00801499,
Coriell:GM12408,
Wikidata:Q54845751
CVCL_5D91 2026-07-25 04:34:54 0
GM12507
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM12507, RRID:CVCL_5U25 Homo sapiens (Human) Miller-Dieker syndrome Finite cell line Male Coriell GM12507 CLO:CLO_0017439,
Coriell:GM12507,
Wikidata:Q54845814
CVCL_5U25 2026-07-25 04:34:56 0
GM16733
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_YP91 Homo sapiens (Human) Population: Caucasian. PMID:23661601 Finite cell line Female Coriell:GM16733,
Wikidata:Q93847995
CVCL_YP91 2026-07-25 04:36:01 0
GM16733
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM16733, RRID:CVCL_YP91 Homo sapiens (Human) Population: Caucasian. PMID:23661601 Finite cell line Female Coriell GM16733 Coriell:GM16733,
Wikidata:Q93847995
CVCL_YP91 2026-07-25 04:36:01 0
GM16735
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM16735, RRID:CVCL_YP92 Homo sapiens (Human) Population: Caucasian. PMID:23661601 Finite cell line Male Coriell GM16735 Coriell:GM16735,
Wikidata:Q93848015
CVCL_YP92 2026-07-25 04:36:01 0
GM17397
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_9Z53 Homo sapiens (Human) Peroxisome biogenesis disorder 7B PMID:16257970 Finite cell line Female Coriell:GM17397,
Wikidata:Q54848828
CVCL_9Z53 2026-07-25 04:36:03 0
GM17731
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_H530 Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 Senescence: Capable of at least 32 PDL (Coriell=GM17731). Finite cell line Male CLO:CLO_0016993,
Coriell:GM17731,
Wikidata:Q54849126
CVCL_H530 2026-07-25 04:36:08 0

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