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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
GM09236
 
Resource Report
Resource Website
RRID:CVCL_AY29 Homo sapiens (Human) Population: African American. PMID:32656337 Transformed cell line Male GM09236A CLO:CLO_0012038,
Coriell:GM09236,
Wikidata:Q54843629
CVCL_AY29 2026-07-25 04:34:04 0
GM09115
 
Resource Report
Resource Website
RRID:CVCL_CY60 Homo sapiens (Human) Gyrate atrophy Population: Caucasian. Finite cell line Female CLO:CLO_0010660,
BioSample:SAMN00798555,
Coriell:GM09115,
Wikidata:Q54843591
CVCL_CY60 2026-07-25 04:34:02 0
GM09213
 
Resource Report
Resource Website
Coriell Cat# GM09213, RRID:CVCL_4H95 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male Coriell GM09213 CLO:CLO_0010690,
Coriell:GM09213,
Wikidata:Q54843615
CVCL_4H95 2026-07-25 04:34:03 0
GM09146
 
Resource Report
Resource Website
Coriell Cat# GM09146, RRID:CVCL_AY28 Homo sapiens (Human) Population: African American. Transformed cell line Female Coriell GM09146 CLO:CLO_0010625,
BioSample:SAMN00798569,
Coriell:GM09146,
Wikidata:Q54843600
CVCL_AY28 2026-07-25 04:34:02 0
GM09239
 
Resource Report
Resource Website
RRID:CVCL_4J58 Homo sapiens (Human) Acute intermittent porphyria Population: Caucasian. Transformed cell line Female CLO:CLO_0012039,
Coriell:GM09239,
Wikidata:Q54843632
CVCL_4J58 2026-07-25 04:34:03 0
GM09091
 
Resource Report
Resource Website
RRID:CVCL_N098 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:16260726
PMID:20889555
PMID:29959025
Transformed cell line Female GM17230 CLO:CLO_0010662,
CLO:CLO_0014347,
BioSample:SAMN00798539,
Coriell:GM09091,
Coriell:GM17230,
GEO:GSM569594,
GEO:GSM596294,
GEO:GSM596654,
GEO:GSM924832,
Wikidata:Q54843573
CVCL_N098 2026-07-25 04:34:02 0
GM09101
 
Resource Report
Resource Website
RRID:CVCL_5N94 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0010655,
BioSample:SAMN00798547,
Coriell:GM09101,
Wikidata:Q54843585
CVCL_5N94 2026-07-25 04:34:02 0
GM09115
 
Resource Report
Resource Website
Coriell Cat# GM09115, RRID:CVCL_CY60 Homo sapiens (Human) Gyrate atrophy Population: Caucasian. Finite cell line Female Coriell GM09115 CLO:CLO_0010660,
BioSample:SAMN00798555,
Coriell:GM09115,
Wikidata:Q54843591
CVCL_CY60 2026-07-25 04:34:02 0
GM09252
 
Resource Report
Resource Website
RRID:CVCL_1L55 Homo sapiens (Human) Population: Caucasian; German/Swiss. Finite cell line Female GM09252A CLO:CLO_0012036,
Coriell:GM09252,
Wikidata:Q54843635
CVCL_1L55 2026-07-25 04:34:03 0
GM09153
 
Resource Report
Resource Website
RRID:CVCL_BT22 Homo sapiens (Human) Beta thalassemia Transformed cell line Female CLO:CLO_0010626,
BioSample:SAMN00798571,
Coriell:GM09153,
Wikidata:Q54843601
CVCL_BT22 2026-07-25 04:34:03 0
GM09193
 
Resource Report
Resource Website
Coriell Cat# GM09193, RRID:CVCL_4H92 Homo sapiens (Human) Manic bipolar affective disorder Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male GM09193A Coriell GM09193 CLO:CLO_0010634,
Coriell:GM09193,
Wikidata:Q54843605
CVCL_4H92 2026-07-25 04:34:02 0
GM09232
 
Resource Report
Resource Website
RRID:CVCL_N101 Homo sapiens (Human) Population: Caucasian; Italian. Finite cell line Male CLO:CLO_0012008,
BioSample:SAMN00798599,
Coriell:GM09232,
Wikidata:Q54843628
CVCL_N101 2026-07-25 04:34:03 0
GM09256
 
Resource Report
Resource Website
RRID:CVCL_V135 Homo sapiens (Human) Population: Caucasian; English/German. PMID:24555846
PMID:25326100
Finite cell line Female GM09256B CLO:CLO_0012022,
Coriell:GM09256,
GEO:GSM1257726,
GEO:GSM1266904,
GEO:GSM1267000,
Wikidata:Q54843638
CVCL_V135 2026-07-25 04:34:03 0
GM09303
 
Resource Report
Resource Website
RRID:CVCL_8A08 Homo sapiens (Human) Transformed cell line Male CLO:CLO_0011878,
Coriell:GM09303,
Wikidata:Q54843663
CVCL_8A08 2026-07-25 04:34:05 0
GM09282
 
Resource Report
Resource Website
RRID:CVCL_1K61 Homo sapiens (Human) Glycogen storage disease type II PMID:1652892 Transformed cell line Female GM 9282 CLO:CLO_0012060,
Coriell:GM09282,
Wikidata:Q54843642
CVCL_1K61 2026-07-25 04:34:04 0
GM09299
 
Resource Report
Resource Website
Coriell Cat# GM09299, RRID:CVCL_AA77 Homo sapiens (Human) Familial dysautonomia Population: Jewish; Ashkenazi. Transformed cell line Female Coriell GM09299 CLO:CLO_0011874,
Coriell:GM09299,
Wikidata:Q54843659
CVCL_AA77 2026-07-25 04:34:04 0
GM09326
 
Resource Report
Resource Website
Coriell Cat# GM09326, RRID:CVCL_W637 Homo sapiens (Human) 47,XYY syndrome Karyotypic information: 47,XYY (Coriell=GM09326)., Population: Caucasian; English/Irish. Finite cell line Male Coriell GM09326 CLO:CLO_0011909,
Coriell:GM09326,
Wikidata:Q54843679
CVCL_W637 2026-07-25 04:34:05 0
GM09359
 
Resource Report
Resource Website
RRID:CVCL_5L85 Homo sapiens (Human) Transformed cell line Male CLO:CLO_0011973,
Coriell:GM09359,
Wikidata:Q54843700
CVCL_5L85 2026-07-25 04:34:04 0
GM09353
 
Resource Report
Resource Website
Coriell Cat# GM09353, RRID:CVCL_5L83 Homo sapiens (Human) Transformed cell line Male Coriell GM09353 CLO:CLO_0011975,
Coriell:GM09353,
Wikidata:Q54843698
CVCL_5L83 2026-07-25 04:34:04 0
GM09349
 
Resource Report
Resource Website
RRID:CVCL_5L81 Homo sapiens (Human) Tuberous sclerosis 2 Transformed cell line Female CLO:CLO_0011977,
Coriell:GM09349,
Wikidata:Q54843696
CVCL_5L81 2026-07-25 04:34:04 0

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