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  • Organism:homo sapiens (human) (facet)

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185,176 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
CCN2.1
 
Resource Report
Resource Website
RRID:CVCL_HM16 Homo sapiens (Human) Donor information: Established from monozygotic twin of CCN2.2 (Cellosaurus=CVCL_HM17). PMID:18435749 Transformed cell line Male GEO:GSM181405,
Wikidata:Q54808987
CVCL_HM16 2026-08-29 04:18:00 0
CCMi005-A
 
Resource Report
Resource Website
RRID:CVCL_B3NP Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian., From: Centro Cardiologico Monzino; Milan; Italy. PMID:35961103 Induced pluripotent stem cell Male DMD4 C3 hPSCreg:CCMi005-A,
Wikidata:Q110432689
CVCL_B3NP 2026-08-29 04:18:00 0
CCMi002-A
 
Resource Report
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RRID:CVCL_RV17 Homo sapiens (Human) Becker's muscular dystrophy Population: Caucasian., From: Centro Cardiologico Monzino; Milan; Italy. PMID:29414413 Induced pluripotent stem cell Male CCMi002BMD-A-9, CCMi002BMD-A-9 delta45-55, BMD1 c.9, BMD1 hPSCreg:CCMi002-A,
Wikidata:Q54808984
CVCL_RV17 2026-08-29 04:18:00 0
CCMBi001-A
 
Resource Report
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RRID:CVCL_YT16 Homo sapiens (Human) Population: Indian., From: Centre for Cellular and Molecular Biology; Hyderabad; India. PMID:32916634 Induced pluripotent stem cell Male M1 hPSCreg:CCMBi001-A,
Wikidata:Q93445506
CVCL_YT16 2026-08-29 04:17:58 0
CCE4.1
 
Resource Report
Resource Website
RRID:CVCL_HM02 Homo sapiens (Human) Childhood absence epilepsy Donor information: Established from monozygotic twin of CCE4.2 (Cellosaurus=CVCL_HM03). PMID:18435749 Transformed cell line Male ConCordant Epilepsy 4.1 GEO:GSM181391,
Wikidata:Q54808953
CVCL_HM02 2026-08-29 04:17:58 0
CCD-974Sk
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_U295 Homo sapiens (Human) Senescence: Senesces at ~13 PDL (ATCC=CRL-1906). Finite cell line Female CCD-974SK, CCD 974 SK ATCC:CRL-1906,
Wikidata:Q54808929
CVCL_U295 2026-08-29 04:17:57 0
CCD-976Sk
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_0F61 Homo sapiens (Human) Finite cell line Male CCD-976SK, CCD 976Sk ATCC:CRL-1904,
Wikidata:Q54808930
CVCL_0F61 2026-08-29 04:17:57 0
CCMi003-A
 
Resource Report
Resource Website
RRID:CVCL_XI81 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian., From: Centro Cardiologico Monzino; Milan; Italy. PMID:31465894 Induced pluripotent stem cell Male DMD3 C2, DMD3 hPSCreg:CCMi003-A,
Wikidata:Q93445530
CVCL_XI81 2026-08-29 04:17:58 0
CCD-977Sk
 
Resource Report
Resource Website
Discontinued
ATCC Cat# CRL-1900, RRID:CVCL_0E73 Homo sapiens (Human) Finite cell line Female ATCC CRL-1900 ATCC:CRL-1900,
BioSample:SAMN03471262,
Wikidata:Q54808931
CVCL_0E73 2026-08-29 04:17:57 0
CCN2.2
 
Resource Report
Resource Website
RRID:CVCL_HM17 Homo sapiens (Human) Donor information: Established from monozygotic twin of CCN2.1 (Cellosaurus=CVCL_HM16). PMID:18435749 Transformed cell line Male GEO:GSM181406,
Wikidata:Q54808995
CVCL_HM17 2026-08-29 04:17:59 0
CCLF-PEDS-0018-T
 
Resource Report
Resource Website
RRID:CVCL_B3PP Homo sapiens (Human) Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE)., Part of: Cancer Cell Line Factory (CCLF) cell models. Undefined cell line type Male CCLF_PEDS_0018_T, CCLFPEDS0018T DepMap:ACH-001767,
Wikidata:Q110432686
CVCL_B3PP 2026-08-29 04:17:58 0
CCD2-iPS 4
 
Resource Report
Resource Website
RRID:CVCL_A4TK Homo sapiens (Human) Cleidocranial dysplasia From: Department of Biochemistry, Tokyo Dental College; Tokyo; Japan. PMID:29357927 Induced pluripotent stem cell Female SKIP:SKIP003021,
Wikidata:Q107114617
CVCL_A4TK 2026-08-29 04:17:57 0
CCK-81
 
Resource Report
Resource Website
RRID:CVCL_2873 Homo sapiens (Human) Colon adenocarcinoma Population: Japanese., Part of: COSMIC cell lines project., Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE)., Part of: AstraZeneca Colorectal cell line (AZCL) panel. PMID:7418977
PMID:9290701
PMID:16418264
PMID:18258742
PMID:20215515
PMID:20606684
PMID:22460905
PMID:23272949
PMID:24755471
PMID:25623215
PMID:25926053
PMID:27397505
PMID:28854368
PMID:29101300
PMID:30894373
PMID:31068700
PMID:31978347
PMID:34466148
PMID:35839778
Cancer cell line Female CCK81 CLO:CLO_0009956,
ArrayExpress:E-MTAB-2770,
ArrayExpress:E-MTAB-3610,
BioGRID_ORCS_Cell_line:593,
BioSample:SAMN03471656,
BioSample:SAMN10987776,
cancercelllines:CVCL_2873,
Cell_Model_Passport:SIDM00487,
ColonAtlas:CCK81,
Cosmic:1187301,
Cosmic:2301965,
Cosmic:2841356,
Cosmic-CLP:1240123,
DepMap:ACH-000963,
EGA:EGAS00001000978,
GDSC:1240123,
GEO:GSM827260,
GEO:GSM886924,
GEO:GSM887990,
GEO:GSM1346831,
GEO:GSM1374444,
GEO:GSM1448097,
GEO:GSM1669669,
GEO:GSM2983077,
GEO:GSM2983078,
GEO:GSM2983079,
GEO:GSM2983080,
IARC_TP53:21737,
JCRB:JCRB0208,
LiGeA:CCLE_532,
LINCS_LDP:LCL-1171,
PharmacoDB:CCK81_189_2019,
PRIDE:PXD005235,
PRIDE:PXD005354,
PRIDE:PXD005355,
PRIDE:PXD030304,
Progenetix:CVCL_2873,
Wikidata:Q54808969
CVCL_2873 2026-08-29 04:17:58 0
CCE2.2
 
Resource Report
Resource Website
RRID:CVCL_HL99 Homo sapiens (Human) Childhood absence epilepsy Donor information: Established from monozygotic twin of CCE2.1 (Cellosaurus=CVCL_HL98). PMID:18435749 Transformed cell line Female ConCordant Epilepsy 2.2 GEO:GSM181385,
Wikidata:Q54808948
CVCL_HL99 2026-08-29 04:17:59 0
CCE4.2
 
Resource Report
Resource Website
RRID:CVCL_HM03 Homo sapiens (Human) Childhood absence epilepsy Donor information: Established from monozygotic twin of CCE4.1 (Cellosaurus=CVCL_HM02). PMID:18435749 Transformed cell line Male ConCordant Epilepsy 4.2 GEO:GSM181392,
Wikidata:Q54808954
CVCL_HM03 2026-08-29 04:17:58 0
CCD-986Sk
 
Resource Report
Resource Website
1+ mentions
ATCC Cat# CRL-1947, RRID:CVCL_2400 Homo sapiens (Human) Senescence: Senesces at ~36 PDL (ATCC=CRL-1947)., Population: African American. Finite cell line Female CCD-986SK, CCD 986 SK, CCD986SK ATCC CRL-1947 BTO:BTO_0005133,
CLO:CLO_0002328,
ATCC:CRL-1947,
BioSample:SAMN03472815,
KCLB:21947,
Wikidata:Q54808933
CVCL_2400 2026-08-29 04:17:57 4
CCH-OS-M
 
Resource Report
Resource Website
RRID:CVCL_XG75 Homo sapiens (Human) Osteosarcoma PMID:22186140 Cancer cell line Wikidata:Q93445414 CVCL_XG75 2026-08-29 04:17:59 0
CCF-STTG1
 
Resource Report
Resource Website
10+ mentions
Discontinued
Discontinued
RRID:CVCL_1118 Homo sapiens (Human) Astrocytoma Population: Caucasian., Part of: PTEN genetic alteration cell panel (ATCC TCP-1030)., Part of: COSMIC cell lines project., Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE). PMID:1404494
PMID:3877740
PMID:19435942
PMID:20164919
PMID:20215515
PMID:22460905
PMID:25877200
PMID:26589293
PMID:27397505
PMID:30894373
PMID:31068700
Cancer cell line Female CCFSTTG1, STTG1 BTO:BTO_0003863,
CLO:CLO_0002329,
EFO:EFO_0002127,
CLDB:cl669,
CLDB:cl5177,
ArrayExpress:E-MTAB-38,
ArrayExpress:E-MTAB-783,
ArrayExpress:E-MTAB-2770,
ArrayExpress:E-MTAB-3610,
ATCC:CRL-1718,
BioGRID_ORCS_Cell_line:591,
BioSample:SAMN01821545,
BioSample:SAMN03470976,
BioSample:SAMN10988114,
cancercelllines:CVCL_1118,
Cell_Model_Passport:SIDM00131,
ChEMBL-Cells:CHEMBL3308795,
ChEMBL-Targets:CHEMBL1075419,
CLS:300388,
Cosmic:687565,
Cosmic:849857,
Cosmic:897441,
Cosmic:906823,
Cosmic:920820,
Cosmic:1175808,
Cosmic:1610750,
Cosmic:1746959,
Cosmic:2302324,
Cosmic:2367511,
Cosmic-CLP:906823,
DepMap:ACH-000329,
ECACC:90021502,
EGA:EGAS00001000978,
GDSC:906823,
GEO:GSM326233,
GEO:GSM886923,
GEO:GSM887989,
GEO:GSM1374443,
GEO:GSM1669668,
IARC_TP53:21217,
IGRhCellID:CCFSTTG1,
IZSLER:BS TCL 125,
LiGeA:CCLE_127,
LINCS_LDP:LCL-1394,
PharmacoDB:CCFSTTG1_188_2019,
PRIDE:PXD003914,
Progenetix:CVCL_1118,
PubChem_Cell_line:CVCL_1118,
RCB:RCB1977,
TKG:TKG 0581,
Wikidata:Q54808966
CVCL_1118 2026-08-29 04:17:58 13
CCD2-iPS 7
 
Resource Report
Resource Website
RRID:CVCL_A4TL Homo sapiens (Human) Cleidocranial dysplasia From: Department of Biochemistry, Tokyo Dental College; Tokyo; Japan. PMID:29357927 Induced pluripotent stem cell Female SKIP:SKIP003021,
Wikidata:Q107114618
CVCL_A4TL 2026-08-29 04:17:57 0
CCD2-iPS 12
 
Resource Report
Resource Website
RRID:CVCL_A4TP Homo sapiens (Human) Cleidocranial dysplasia From: Department of Biochemistry, Tokyo Dental College; Tokyo; Japan. PMID:29357927 Induced pluripotent stem cell Female SKIP:SKIP003021,
Wikidata:Q107114616
CVCL_A4TP 2026-08-29 04:17:59 0

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