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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
FCP-S4H
 
Resource Report
Resource Website
RCB Cat# RCB0786, RRID:CVCL_L887 Homo sapiens (Human) Donor information: Established from a patient suffering from familial colon polyposis., Population: Japanese. Finite cell line Female RCB RCB0786 CLO:CLO_0050684,
BioSample:SAMN03472235,
RCB:RCB0786,
Wikidata:Q54833425
CVCL_L887 2026-09-12 05:31:02 0
FDCHi003-A
 
Resource Report
Resource Website
RRID:CVCL_A1DF Homo sapiens (Human) Alstrom syndrome Population: Chinese., From: Children's Hospital of Fudan University; Shanghai; China. PMID:33264725 Induced pluripotent stem cell Male iPSx-y-ALMS1-m hPSCreg:FDCHi003-A,
Wikidata:Q102113815
CVCL_A1DF 2026-09-12 05:31:02 0
Fe Bos
 
Resource Report
Resource Website
ATCC Cat# CRL-1177, RRID:CVCL_3303 Homo sapiens (Human) Ehlers-Danlos syndrome, type II Finite cell line Female ATCC CRL-1177 CLO:CLO_0003075,
ATCC:CRL-1177,
Wikidata:Q54834712
CVCL_3303 2026-09-12 05:31:02 0
FE0001
 
Resource Report
Resource Website
Discontinued
ECACC Cat# 94100312, RRID:CVCL_8W22 Homo sapiens (Human) Holoprosencephaly Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 94100312 ECACC:94100312,
Wikidata:Q54834717
CVCL_8W22 2026-09-12 05:31:02 0
FDEENTi001-A
 
Resource Report
Resource Website
RRID:CVCL_UM43 Homo sapiens (Human) Pathological myopia Population: Chinese; Han., From: Eye & ENT Hospital, Shanghai Medical School, Fudan University; Shanghai; China. PMID:30611020 Induced pluripotent stem cell Male LP-IPS BioSamples:SAMEA5309469,
hPSCreg:FDEENTi001-A,
SKIP:SKIP005539,
Wikidata:Q93551907
CVCL_UM43 2026-09-12 05:31:02 0
FDC-P1
 
Resource Report
Resource Website
RRID:CVCL_2039 Mus musculus (Mouse) Caution: According to PubMed=6968334 originate from DBA/2 mice but in the original deposit document for DSMZ ACC-268 it is said to originate from C57BL/6 x DBA/2 (B6D2F1) (personal communication of MacLeod, Roderick A.F.)., Characteristics: IL3 dependent. PMID:2656885
PMID:6968334
Factor-dependent cell line FDCP-1, FDCP1, Factor Dependent Continuous-Paterson 1, Factor Dependent Cell-Paterson 1 BTO:BTO_0000595,
CLO:CLO_0003072,
CLO:CLO_0003073,
EFO:EFO_0022739,
ATCC:CRL-12103,
BCRJ:0086,
CCRID:1101MOU-PUMC000007,
DSMZ:ACC-368,
DSMZCellDive:ACC-368,
Lonza:759,
Wikidata:Q27653134
CVCL_2039 2026-09-12 05:31:02 0
FE0001
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_8W22 Homo sapiens (Human) Holoprosencephaly Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:94100312,
Wikidata:Q54834717
CVCL_8W22 2026-09-12 05:31:02 0
FE0002
 
Resource Report
Resource Website
Discontinued
ECACC Cat# 94110944, RRID:CVCL_8W23 Homo sapiens (Human) VACTERL association Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 94110944 ECACC:94110944,
Wikidata:Q54834718
CVCL_8W23 2026-09-12 05:31:03 0
FE0008
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_8W26 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:95033056,
Wikidata:Q54834721
CVCL_8W26 2026-09-12 05:31:03 0
FG-9307
 
Resource Report
Resource Website
RRID:CVCL_8197 Paralichthys olivaceus (Bastard halibut) Group: Fish cell line. Spontaneously immortalized cell line Sex unspecified FG9307, Flounder Gill-9307, FG BTO:BTO_0006536,
CCTCC:GDC0194,
Wikidata:Q54834780
CVCL_8197 2026-09-12 05:31:04 0
Fer Ray
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_H577 Homo sapiens (Human) Ehlers-Danlos syndrome, type III Finite cell line Male CLO:CLO_0003082,
CLDB:cl1224,
ATCC:CRL-1156,
Wikidata:Q54834756
CVCL_H577 2026-09-12 05:31:03 0
FEH18L
 
Resource Report
Resource Website
RRID:CVCL_LC32 Homo sapiens (Human) PMID:2479170
PMID:2558081
Transformed cell line Male Wikidata:Q54834738 CVCL_LC32 2026-09-12 05:31:03 0
FE0037
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_8W34 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:97040402,
Wikidata:Q54834729
CVCL_8W34 2026-09-12 05:31:03 0
FF101
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_8562 Rattus norvegicus (Rat) Rat hepatocellular carcinoma Group: Serum/protein free medium cell line. PMID:1281996
PMID:2702652
Cancer cell line Male JCRB:JCRB1040,
JCRB:NIHS0323,
Wikidata:Q54834772
CVCL_8562 2026-09-12 05:31:04 0
FF
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_U308 Mesocricetus auratus (Golden hamster) Hamster melanoma Characteristics: Pigmented. PMID:3734481
PMID:4522794
PMID:5556532
Cancer cell line Sex unspecified ATCC:CRL-1479,
Wikidata:Q54834769
cvcl_2711 CVCL_U308 2026-09-12 05:31:04 0
FG4003
 
Resource Report
Resource Website
RRID:CVCL_ZT69 Homo sapiens (Human) Ataxia-oculomotor apraxia type 1 PMID:15044383 Finite cell line Wikidata:Q98126025 CVCL_ZT69 2026-09-12 05:31:04 0
FFB-L3
 
Resource Report
Resource Website
KCB Cat# KCB 200520LZJ, RRID:CVCL_A9HS Rousettus leschenaultii (Leschenault's rousette) Group: Bat cell line. Finite cell line Female FFBL3 KCB KCB 200520LZJ CCRID:5301MAM-KCB0520LZJ,
KCB:KCB 200520LZJ,
Wikidata:Q108820237
CVCL_A9HS 2026-09-12 05:31:04 0
FES 22
 
Resource Report
Resource Website
RRID:CVCL_B133 Homo sapiens (Human) From: University of Helsinki; Helsinki; Finland. PMID:16895598
PMID:17572666
Embryonic stem cell Male FES22, UHe002-A hPSCreg:UHe002-A,
IGRhCellID:FES22%20p41-2,
SKIP:SKIP001848,
Wikidata:Q54834758
CVCL_B133 2026-09-12 05:31:03 0
FEPE1L-9
 
Resource Report
Resource Website
RRID:CVCL_LC36 Homo sapiens (Human) PMID:2543780
PMID:2558081
Transformed cell line Male FEPE1L9 Wikidata:Q54834754 CVCL_LC36 2026-09-12 05:31:03 0
FES 75
 
Resource Report
Resource Website
RRID:CVCL_B137 Homo sapiens (Human) From: University of Helsinki; Helsinki; Finland. Embryonic stem cell Male FES75, UHe006-A hPSCreg:UHe006-A,
IGRhCellID:FES75%20p19-2,
SKIP:SKIP001852,
Wikidata:Q54834762
CVCL_B137 2026-09-12 05:31:03 0

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