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6,967 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
HERLUF
 
Resource Report
Resource Website
ECACC Cat# 87031104, RRID:CVCL_E693 Homo sapiens (Human) Population: Caucasian; Danish., Part of: 12th International Histocompatibility Workshop (12IHW) cell line panel. PMID:6200433
PMID:29171935
PMID:30844424
Transformed cell line Male HERLUF2, HERLUFF, Herluff, GM03160, GM3160 ECACC 87031104 CLO:CLO_0013515,
Coriell:GM03160,
dbMHC:48889,
ECACC:87031104,
IHW:IHW09299,
IPD-IMGT/HLA:10728,
Wikidata:Q54882891
CVCL_E693 2026-08-29 04:36:59 0
HEPM
 
Resource Report
Resource Website
1+ mentions
ECACC Cat# 90120505, RRID:CVCL_2486 Homo sapiens (Human) PMID:1282915
PMID:7017936
PMID:7119095
Finite cell line Female Human Embryonic Palatal Mesenchyme ECACC 90120505 CLO:CLO_0003714,
CLDB:cl1662,
ATCC:CRL-1486,
BCRC:60277,
BioSample:SAMN03471366,
ECACC:90120505,
FANTOM5_SSTAR:10813-111B3,
IZSLER:BS CL 163,
JCRB:JCRB9095,
Wikidata:Q54882874
CVCL_2486 2026-08-29 04:36:59 2
HF2x653
 
Resource Report
Resource Website
ECACC Cat# 90012609, RRID:CVCL_2488 Homo sapiens (Human) Group: Hybridoma fusion partner cell line. Hybrid cell line ECACC 90012609 CLO:CLO_0003728,
CLDB:cl1667,
ECACC:90012609,
NCBI_Iran:C150,
Wikidata:Q54883249
CVCL_2488 2026-08-29 04:37:09 0
HG-261
 
Resource Report
Resource Website
Possibly Discontinued
Possibly Discontinued
Possibly Discontinued
ECACC Cat# 93120823, RRID:CVCL_2490 Homo sapiens (Human) Fanconi anemia Population: Caucasian. PMID:420857
PMID:656543
PMID:7374661
PMID:7471105
Finite cell line Male HG 261, HG261, GM00062, GM62, GM 62 ECACC 93120823 CLO:CLO_0003738,
CLDB:cl1671,
CLDB:cl1672,
ATCC:CCL-122,
BioSample:SAMN03472702,
Coriell:GM00062,
ECACC:90112603,
ECACC:93120823,
IZSLER:BS TCL 24,
Wikidata:Q54883309
CVCL_2490 2026-08-29 04:37:11 0
HG-261
 
Resource Report
Resource Website
Possibly Discontinued
Possibly Discontinued
Possibly Discontinued
ECACC Cat# 90112603, RRID:CVCL_2490 Homo sapiens (Human) Fanconi anemia Population: Caucasian. PMID:420857
PMID:656543
PMID:7374661
PMID:7471105
Finite cell line Male HG 261, HG261, GM00062, GM62, GM 62 ECACC 90112603 CLO:CLO_0003738,
CLDB:cl1671,
CLDB:cl1672,
ATCC:CCL-122,
BioSample:SAMN03472702,
Coriell:GM00062,
ECACC:90112603,
ECACC:93120823,
IZSLER:BS TCL 24,
Wikidata:Q54883309
CVCL_2490 2026-08-29 04:37:10 0
HMy2.C1R
 
Resource Report
Resource Website
1+ mentions
ECACC Cat# 94050320, RRID:CVCL_3714 Homo sapiens (Human) Population: Caucasian., Part of: 12th International Histocompatibility Workshop (12IHW) cell line panel. PMID:1541831
PMID:2784569
PMID:3819393
PMID:30844424
Transformed cell line Female Hmy.2 CIR, HMy2.CIR, C1R ECACC 94050320 BTO:BTO_0003699,
CLO:CLO_0003787,
ATCC:CRL-1993,
CCRID:3101HUMGNHu21,
ChEMBL-Cells:CHEMBL4295449,
ChEMBL-Targets:CHEMBL4296434,
CLS:305126,
dbMHC:48526,
ECACC:94050320,
IHW:IHW09208,
IPD-IMGT/HLA:10372,
Lonza:1264,
PubChem_Cell_line:CVCL_3714,
Wikidata:Q54889982
cvcl_8119 CVCL_3714 2026-08-29 04:39:08 2
HMT-3522 S1
 
Resource Report
Resource Website
1+ mentions
ECACC Cat# 98102210, RRID:CVCL_2499 Homo sapiens (Human) Donor information: Established from a nontumorigenic fibrocystic breast lesion (from parent cell line HMT-3522)., Population: Caucasian., Part of: JWGray breast cancer cell line panel. PMID:7982476
PMID:8616848
PMID:16849555
PMID:18316601
PMID:18516279
PMID:22414580
PMID:24176112
Spontaneously immortalized cell line Female HMT-3522-S1, HMT3522 S1, HMT-3522S1, HMT3522S1, S1, S-1, HMT-3522/wt, HMEC S1 ECACC 98102210 BTO:BTO_0006484,
EFO:EFO_0001191,
ArrayExpress:E-TABM-244,
Cosmic:889085,
ECACC:98102210,
GEO:GSM200612,
GEO:GSM200739,
GEO:GSM200740,
GEO:GSM200741,
GEO:GSM200742,
GEO:GSM200743,
GEO:GSM1219374,
GEO:GSM1219375,
GEO:GSM1219376,
GEO:GSM1219377,
GEO:GSM1219378,
LINCS_HMS:51119,
PharmacoDB:S1_1340_2019,
PRIDE:PXD000309,
Wikidata:Q54889968
cvcl_6855 CVCL_2499 2026-08-29 04:39:08 1
HO301
 
Resource Report
Resource Website
ECACC Cat# 88052055, RRID:CVCL_E701 Homo sapiens (Human) Population: Caucasian; French., Part of: 10th International Histocompatibility Workshop (10IHW) cell line panel. PMID:8307784
PMID:8813743
PMID:29171935
PMID:30844424
Transformed cell line Female H0301, HO 301 ECACC 88052055 dbMHC:48876,
ECACC:88052055,
IHW:IHW09055,
IPD-IMGT/HLA:10751,
Wikidata:Q54890095
CVCL_E701 2026-08-29 04:39:11 0
HO104
 
Resource Report
Resource Website
ECACC Cat# 88052082, RRID:CVCL_E700 Homo sapiens (Human) Population: Caucasian; French., Part of: 10th International Histocompatibility Workshop (10IHW) cell line panel. PMID:8307784
PMID:8813743
PMID:28360230
PMID:29171935
PMID:30844424
Transformed cell line Male H0104, HO 104 ECACC 88052082 dbMHC:48896,
ECACC:88052082,
IHW:IHW09082,
IPD-IMGT/HLA:11633,
Wikidata:Q54890091
CVCL_E700 2026-08-29 04:39:10 0
HOKKAIDO
 
Resource Report
Resource Website
ECACC Cat# 94082241, RRID:CVCL_E702 Homo sapiens (Human) Population: Asian., Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel. PMID:8307784
PMID:30844424
Transformed cell line Male ECACC 94082241 dbMHC:48897,
ECACC:94082241,
IHW:IHW09141,
IPD-IMGT/HLA:11684,
Wikidata:Q54890139
CVCL_E702 2026-08-29 04:39:11 0
HH0008
 
Resource Report
Resource Website
ECACC Cat# 89030660, RRID:CVCL_8W63 Homo sapiens (Human) Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 89030660 ECACC:89030660,
Wikidata:Q54887347
CVCL_8W63 2026-08-29 04:38:56 0
HH0020
 
Resource Report
Resource Website
ECACC Cat# 89030640, RRID:CVCL_8W72 Homo sapiens (Human) Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 89030640 ECACC:89030640,
Wikidata:Q54887356
CVCL_8W72 2026-08-29 04:38:56 0
HH0027
 
Resource Report
Resource Website
ECACC Cat# 89030625, RRID:CVCL_8W77 Homo sapiens (Human) Karyotypic information: 47,XX,inv dup(15)(q11.2) (ECACC=89030625)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 89030625 ECACC:89030625,
Wikidata:Q54887363
CVCL_8W77 2026-08-29 04:38:54 0
HH0004
 
Resource Report
Resource Website
ECACC Cat# 910430171, RRID:CVCL_8W59 Homo sapiens (Human) Karyotypic information: 46,Y,Xp- (ECACC=910430171)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 910430171 ECACC:910430171,
Wikidata:Q54887343
CVCL_8W59 2026-08-29 04:38:53 0
HH0005
 
Resource Report
Resource Website
ECACC Cat# 89030635, RRID:CVCL_8W60 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 89030635 ECACC:89030635,
Wikidata:Q54887344
CVCL_8W60 2026-08-29 04:38:56 0
HH0025
 
Resource Report
Resource Website
ECACC Cat# 89030628, RRID:CVCL_8W76 Homo sapiens (Human) Karyotypic information: 46,XX,-18,+i(18q); 47,XX,-18,+i(18q)+i(18p) (ECACC=89030628)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 89030628 ECACC:89030628,
Wikidata:Q54887362
CVCL_8W76 2026-08-29 04:38:54 0
HH0117
 
Resource Report
Resource Website
ECACC Cat# 89042115, RRID:CVCL_8X14 Homo sapiens (Human) Karyotypic information: 46,XX,t(2;9)(p11.2;p13) (ECACC=89042115)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 89042115 ECACC:89042115,
Wikidata:Q54887407
CVCL_8X14 2026-08-29 04:38:55 0
HH0094
 
Resource Report
Resource Website
ECACC Cat# 89061910, RRID:CVCL_8X00 Homo sapiens (Human) Karyotypic information: 47,XX,+i(12p) (ECACC=89061910)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 89061910 ECACC:89061910,
Wikidata:Q54887387
CVCL_8X00 2026-08-29 04:38:54 0
HH0106
 
Resource Report
Resource Website
ECACC Cat# 89041151, RRID:CVCL_8X08 Homo sapiens (Human) Karyotypic information: 46,X,dup(Xq) (ECACC=89041151)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 89041151 ECACC:89041151,
Wikidata:Q54887396
CVCL_8X08 2026-08-29 04:38:54 0
HH0092
 
Resource Report
Resource Website
ECACC Cat# 89041120, RRID:CVCL_8W98 Homo sapiens (Human) Karyotypic information: 46,X,inv(X)(p11;q28) (ECACC=89041120)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 89041120 ECACC:89041120,
Wikidata:Q54887385
CVCL_8W98 2026-08-29 04:38:54 0

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