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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
GM13277
 
Resource Report
Resource Website
Coriell Cat# GM13277, RRID:CVCL_5P73 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM13277 CLO:CLO_0013290,
BioSample:SAMN00802246,
Coriell:GM13277,
Wikidata:Q54846416
CVCL_5P73 2026-08-01 05:07:01 0
GM13302
 
Resource Report
Resource Website
Coriell Cat# GM13302, RRID:CVCL_1S67 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. PMID:8404043 Hybrid cell line UMHG-17/1A Coriell GM13302 CLO:CLO_0013321,
Coriell:GM13302,
Wikidata:Q54846432
cvcl_k265 CVCL_1S67 2026-08-01 05:07:02 0
GM13266
 
Resource Report
Resource Website
Coriell Cat# GM13266, RRID:CVCL_4F66 Homo sapiens (Human) Zellweger syndrome Population: Caucasian. Finite cell line Male Coriell GM13266 CLO:CLO_0013126,
BioSample:SAMN00802230,
Coriell:GM13266,
Wikidata:Q54846408
CVCL_4F66 2026-08-01 05:07:01 0
GM13276
 
Resource Report
Resource Website
Coriell Cat# GM13276, RRID:CVCL_GZ47 Homo sapiens (Human) Congenital bilateral aplasia of the vas deferens Transformed cell line Male Coriell GM13276 CLO:CLO_0013289,
BioSample:SAMN00802244,
Coriell:GM13276,
Wikidata:Q54846415
CVCL_GZ47 2026-08-01 05:07:07 0
GM13287
 
Resource Report
Resource Website
RRID:CVCL_4Z71 Homo sapiens (Human) Trichothiodystrophy Population: Caucasian. Finite cell line Male CLO:CLO_0013352,
BioSample:SAMN00802258,
Coriell:GM13287,
Wikidata:Q54846422
CVCL_4Z71 2026-08-01 05:07:04 0
GM13310
 
Resource Report
Resource Website
Coriell Cat# GM13310, RRID:CVCL_4F06 Homo sapiens (Human) Ellis-Van Creveld syndrome Population: Caucasian; Amish. Transformed cell line Female Coriell GM13310 CLO:CLO_0013244,
BioSample:SAMN00802285,
Coriell:GM13310,
Wikidata:Q54846450
CVCL_4F06 2026-08-01 05:07:04 0
GM13247
 
Resource Report
Resource Website
Coriell Cat# GM13247, RRID:CVCL_V395 Homo sapiens (Human) Glycogen storage disease type Ia Transformed cell line Male Coriell GM13247 CLO:CLO_0013186,
BioSample:SAMN00802206,
Coriell:GM13247,
Wikidata:Q54846393
CVCL_V395 2026-08-01 05:07:01 0
GM13263
 
Resource Report
Resource Website
RRID:CVCL_BW65 Homo sapiens (Human) D-bifunctional protein deficiency Population: African American. Finite cell line Male CLO:CLO_0013114,
BioSample:SAMN00802224,
Coriell:GM13263,
Wikidata:Q54846405
CVCL_BW65 2026-08-01 05:07:06 0
GM13249
 
Resource Report
Resource Website
Coriell Cat# GM13249, RRID:CVCL_V138 Homo sapiens (Human) Von Hippel-Lindau syndrome Transformed cell line Male Coriell GM13249 CLO:CLO_0013079,
Coriell:GM13249,
Wikidata:Q54846395
CVCL_V138 2026-08-01 05:07:01 0
GM13248
 
Resource Report
Resource Website
RRID:CVCL_V137 Homo sapiens (Human) Von Hippel-Lindau syndrome Transformed cell line Male CLO:CLO_0013074,
BioSample:SAMN00802208,
Coriell:GM13248,
Wikidata:Q54846394
CVCL_V137 2026-08-01 05:07:06 0
GM13309
 
Resource Report
Resource Website
Coriell Cat# GM13309, RRID:CVCL_4F05 Homo sapiens (Human) Ellis-Van Creveld syndrome Population: Caucasian; Amish. Transformed cell line Female Coriell GM13309 CLO:CLO_0013245,
BioSample:SAMN00802283,
Coriell:GM13309,
Wikidata:Q54846449
CVCL_4F05 2026-08-01 05:07:02 0
GM13267
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM13267, RRID:CVCL_4F67 Homo sapiens (Human) Zellweger syndrome Population: Caucasian. Finite cell line Male Coriell GM13267 CLO:CLO_0013123,
BioSample:SAMN00802232,
Coriell:GM13267,
Wikidata:Q54846409
CVCL_4F67 2026-08-01 05:07:03 1
GM13251
 
Resource Report
Resource Website
RRID:CVCL_V140 Homo sapiens (Human) Von Hippel-Lindau syndrome Transformed cell line Male CLO:CLO_0013085,
Coriell:GM13251,
Wikidata:Q54846397
CVCL_V140 2026-08-01 05:07:01 0
GM13257
 
Resource Report
Resource Website
RRID:CVCL_V145 Homo sapiens (Human) Von Hippel-Lindau syndrome Transformed cell line Male CLO:CLO_0013060,
BioSample:SAMN00802220,
Coriell:GM13257,
Wikidata:Q54846403
CVCL_V145 2026-08-01 05:07:01 0
GM13312
 
Resource Report
Resource Website
Coriell Cat# GM13312, RRID:CVCL_4F08 Homo sapiens (Human) Ellis-Van Creveld syndrome Population: Caucasian; Amish. Transformed cell line Male Coriell GM13312 CLO:CLO_0013216,
BioSample:SAMN00802289,
Coriell:GM13312,
Wikidata:Q54846452
CVCL_4F08 2026-08-01 05:07:02 0
GM13286
 
Resource Report
Resource Website
Coriell Cat# GM13286, RRID:CVCL_4Z70 Homo sapiens (Human) Trichothiodystrophy Population: Caucasian. Transformed cell line Male GM13286A Coriell GM13286 CLO:CLO_0013300,
BioSample:SAMN00802256,
Coriell:GM13286,
Wikidata:Q54846421
CVCL_4Z70 2026-08-01 05:07:07 0
GM133
 
Resource Report
Resource Website
RRID:CVCL_B4FS Homo sapiens (Human) Glioblastoma Characteristics: Early passage culture. PMID:14961077
PMID:23541792
Cancer cell line Sex unspecified cancercelllines:CVCL_B4FS,
IARC_TP53:20808,
Wikidata:Q110432814
CVCL_B4FS 2026-08-01 05:07:04 0
GM13313
 
Resource Report
Resource Website
RRID:CVCL_4F09 Homo sapiens (Human) Ellis-Van Creveld syndrome Population: Caucasian; Amish. Transformed cell line Female CLO:CLO_0013217,
BioSample:SAMN00802291,
Coriell:GM13313,
Wikidata:Q54846453
CVCL_4F09 2026-08-01 05:07:08 0
GM13205
 
Resource Report
Resource Website
RRID:CVCL_AX25 Homo sapiens (Human) Niemann-Pick disease, type A Population: Jewish; Ashkenazi., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:19815695
PMID:21335555
Finite cell line Female NPD-1 BTO:BTO_0004931,
CLO:CLO_0013203,
Coriell:GM13205,
Wikidata:Q54846381
CVCL_AX25 2026-08-01 05:07:05 0
GM13254
 
Resource Report
Resource Website
Coriell Cat# GM13254, RRID:CVCL_V142 Homo sapiens (Human) Von Hippel-Lindau syndrome Transformed cell line Male Coriell GM13254 CLO:CLO_0013093,
BioSample:SAMN00802214,
Coriell:GM13254,
Wikidata:Q54846399
CVCL_V142 2026-08-01 05:07:06 0

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