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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
GM09146
 
Resource Report
Resource Website
RRID:CVCL_AY28 Homo sapiens (Human) Population: African American. Transformed cell line Female CLO:CLO_0010625,
BioSample:SAMN00798569,
Coriell:GM09146,
Wikidata:Q54843600
CVCL_AY28 2026-07-25 04:34:02 0
GM09194
 
Resource Report
Resource Website
RRID:CVCL_1L29 Homo sapiens (Human) Menkes disease Population: Caucasian. Transformed cell line Male CLO:CLO_0010637,
BioSample:SAMN00798579,
Coriell:GM09194,
Wikidata:Q54843606
CVCL_1L29 2026-07-25 04:34:03 0
GM09145
 
Resource Report
Resource Website
Coriell Cat# GM09145, RRID:CVCL_AY27 Homo sapiens (Human) Fragile X syndrome Population: African American. PMID:1672039 Transformed cell line Male GM9145 Coriell GM09145 CLO:CLO_0010628,
BioSample:SAMN00798567,
Coriell:GM09145,
Wikidata:Q54843599
CVCL_AY27 2026-07-25 04:34:03 0
GM09112
 
Resource Report
Resource Website
RRID:CVCL_CY58 Homo sapiens (Human) Gyrate atrophy Population: Caucasian. Finite cell line Female GM09112A CLO:CLO_0010658,
BioSample:SAMN00798551,
Coriell:GM09112,
Wikidata:Q54843589
CVCL_CY58 2026-07-25 04:34:02 0
GM09197
 
Resource Report
Resource Website
RRID:CVCL_W576 Homo sapiens (Human) Huntington's disease Population: Caucasian. PMID:25732146
PMID:25928884
Finite cell line Male CLO:CLO_0010640,
BioSample:SAMN00798585,
Coriell:GM09197,
Wikidata:Q54843609
CVCL_W576 2026-07-25 04:34:02 0
GM09090
 
Resource Report
Resource Website
RRID:CVCL_W300 Homo sapiens (Human) Usher syndrome type 1 Population: Caucasian; Acadian. Transformed cell line Male CLO:CLO_0010647,
BioSample:SAMN00798537,
Coriell:GM09090,
Wikidata:Q54843572
CVCL_W300 2026-07-25 04:34:02 0
GM09238
 
Resource Report
Resource Website
RRID:CVCL_AY31 Homo sapiens (Human) Population: African American. PMID:1672039 Transformed cell line Female GM9238 CLO:CLO_0012040,
Coriell:GM09238,
Wikidata:Q54843631
CVCL_AY31 2026-07-25 04:34:04 0
GM09142
 
Resource Report
Resource Website
RRID:CVCL_1R81 Homo sapiens (Human) Characteristics: Hybrid for chromosome X mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid. PMID:9441767 Hybrid cell line C2-T10 CLO:CLO_0010627,
Coriell:GM09142,
Wikidata:Q54843598
cvcl_3984 CVCL_1R81 2026-07-25 04:34:03 0
GM09142
 
Resource Report
Resource Website
Coriell Cat# GM09142, RRID:CVCL_1R81 Homo sapiens (Human) Characteristics: Hybrid for chromosome X mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid. PMID:9441767 Hybrid cell line C2-T10 Coriell GM09142 CLO:CLO_0010627,
Coriell:GM09142,
Wikidata:Q54843598
cvcl_3984 CVCL_1R81 2026-07-25 04:34:02 0
GM09196
 
Resource Report
Resource Website
RRID:CVCL_N100 Homo sapiens (Human) Population: Caucasian; Italian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:29959025
Transformed cell line Male GM17231 CLO:CLO_0010639,
CLO:CLO_0014341,
BioSample:SAMN00798583,
Coriell:GM09196,
Coriell:GM17231,
GEO:GSM569606,
GEO:GSM596295,
GEO:GSM596655,
GEO:GSM924833,
Wikidata:Q54843608
CVCL_N100 2026-07-25 04:34:02 0
GM09218
 
Resource Report
Resource Website
RRID:CVCL_AA71 Homo sapiens (Human) Crigler-Najjar syndrome Transformed cell line Male CLO:CLO_0010683,
BioSample:SAMN00798591,
Coriell:GM09218,
Wikidata:Q54843620
CVCL_AA71 2026-07-25 04:34:04 0
GM09101
 
Resource Report
Resource Website
Coriell Cat# GM09101, RRID:CVCL_5N94 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM09101 CLO:CLO_0010655,
BioSample:SAMN00798547,
Coriell:GM09101,
Wikidata:Q54843585
CVCL_5N94 2026-07-25 04:34:02 0
GM09189
 
Resource Report
Resource Website
Coriell Cat# GM09189, RRID:CVCL_5N97 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell GM09189 CLO:CLO_0010631,
BioSample:SAMN00798575,
Coriell:GM09189,
Wikidata:Q54843603
CVCL_5N97 2026-07-25 04:34:02 0
GM09145
 
Resource Report
Resource Website
RRID:CVCL_AY27 Homo sapiens (Human) Fragile X syndrome Population: African American. PMID:1672039 Transformed cell line Male GM9145 CLO:CLO_0010628,
BioSample:SAMN00798567,
Coriell:GM09145,
Wikidata:Q54843599
CVCL_AY27 2026-07-25 04:34:02 0
GM09116
 
Resource Report
Resource Website
Coriell Cat# GM09116, RRID:CVCL_CY61 Homo sapiens (Human) Gyrate atrophy Population: Caucasian. Finite cell line Female Coriell GM09116 CLO:CLO_0010661,
BioSample:SAMN00798557,
Coriell:GM09116,
Wikidata:Q54843592
CVCL_CY61 2026-07-25 04:34:02 0
GM09117
 
Resource Report
Resource Website
RRID:CVCL_CY62 Homo sapiens (Human) Gyrate atrophy Population: Caucasian. Finite cell line Female CLO:CLO_0010623,
BioSample:SAMN00798559,
Coriell:GM09117,
Wikidata:Q54843593
CVCL_CY62 2026-07-25 04:34:02 0
GM09216
 
Resource Report
Resource Website
Coriell Cat# GM09216, RRID:CVCL_V823 Homo sapiens (Human) Population: African American. PMID:23665875 Transformed cell line Male Coriell GM09216 CLO:CLO_0010685,
BioSample:SAMN00798587,
Coriell:GM09216,
Wikidata:Q54843618
CVCL_V823 2026-07-25 04:34:03 0
GM09196
 
Resource Report
Resource Website
Coriell Cat# GM09196, RRID:CVCL_N100 Homo sapiens (Human) Population: Caucasian; Italian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:29959025
Transformed cell line Male GM17231 Coriell GM09196 CLO:CLO_0010639,
CLO:CLO_0014341,
BioSample:SAMN00798583,
Coriell:GM09196,
Coriell:GM17231,
GEO:GSM569606,
GEO:GSM596295,
GEO:GSM596655,
GEO:GSM924833,
Wikidata:Q54843608
CVCL_N100 2026-07-25 04:34:02 0
GM09113
 
Resource Report
Resource Website
RRID:CVCL_CY59 Homo sapiens (Human) Gyrate atrophy Population: Caucasian; Irish. PMID:10617919 Finite cell line Female CLO:CLO_0010659,
BioSample:SAMN00798553,
Coriell:GM09113,
Wikidata:Q54843590
CVCL_CY59 2026-07-25 04:34:03 0
GM09246
 
Resource Report
Resource Website
RRID:CVCL_1L53 Homo sapiens (Human) Population: Caucasian; German/Swiss. Finite cell line Female GM09246A, GM09246B CLO:CLO_0012033,
Coriell:GM09246,
Wikidata:Q54843633
CVCL_1L53 2026-07-25 04:34:04 0

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