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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
Dch3
 
Resource Report
Resource Website
Possibly Discontinued
JCRB Cat# JCRB3003, RRID:CVCL_F011 Homo sapiens (Human) Dyschromatosis symmetrica hereditaria Population: Japanese. Finite cell line Male JCRB JCRB3003 BioSample:SAMN03472403,
JCRB:JCRB3003,
JCRB:KURB2100,
Wikidata:Q54828676
CVCL_F011 2026-08-15 04:26:10 0
DD0006
 
Resource Report
Resource Website
RRID:CVCL_8U28 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:90012933,
Wikidata:Q54828706
CVCL_8U28 2026-08-15 04:26:10 0
DCR7
 
Resource Report
Resource Website
RRID:CVCL_EI69 Homo sapiens (Human) Colorectal carcinoma Population: Caucasian. PMID:22270724 Cancer cell line Female DCR 7 cancercelllines:CVCL_EI69,
ColonAtlas:DCR7,
Cosmic:1690657,
Wikidata:Q54828679
cvcl_6895 CVCL_EI69 2026-08-15 04:26:09 0
DCE5.2
 
Resource Report
Resource Website
RRID:CVCL_HM13 Homo sapiens (Human) Donor information: Established from monozygotic twin of DCE5.1 (Cellosaurus=CVCL_HM12). PMID:18435749 Transformed cell line Female GEO:GSM181380,
Wikidata:Q54828655
CVCL_HM13 2026-08-15 04:26:09 0
DD0020
 
Resource Report
Resource Website
ECACC Cat# 90032811, RRID:CVCL_8U34 Homo sapiens (Human) Karyotypic information: 46,Y,del(X)(pter->q21.1::q21.2->qter)mat (ECACC=90032811)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 90032811 ECACC:90032811,
Wikidata:Q54828712
CVCL_8U34 2026-08-15 04:26:11 0
DCH001
 
Resource Report
Resource Website
RRID:CVCL_E546 Homo sapiens (Human) Population: Southeast Asian; Thai., Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel. PMID:8307784 Transformed cell line Sex unspecified DCH 001, DCH-001 dbMHC:48744,
IHW:IHW09181,
IPD-IMGT/HLA:11723,
Wikidata:Q54828656
CVCL_E546 2026-08-15 04:26:09 0
DD0005
 
Resource Report
Resource Website
ECACC Cat# 89111401, RRID:CVCL_8U27 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 89111401 ECACC:89111401,
Wikidata:Q54828705
CVCL_8U27 2026-08-15 04:26:10 0
DD0026
 
Resource Report
Resource Website
RRID:CVCL_8U39 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:90060803,
Wikidata:Q54828717
CVCL_8U39 2026-08-15 04:26:11 0
DCH006
 
Resource Report
Resource Website
ECACC Cat# 94082288, RRID:CVCL_E550 Homo sapiens (Human) Population: Southeast Asian; Thai., Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel. PMID:8307784
PMID:30844424
Transformed cell line Female DCH 006, DCH-006, Thai-DCH006 ECACC 94082288 dbMHC:48746,
ECACC:94082288,
IHW:IHW09188,
IPD-IMGT/HLA:11730,
Wikidata:Q54828658
CVCL_E550 2026-08-15 04:26:09 0
DD0006
 
Resource Report
Resource Website
ECACC Cat# 90012933, RRID:CVCL_8U28 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 90012933 ECACC:90012933,
Wikidata:Q54828706
CVCL_8U28 2026-08-15 04:26:11 0
Dch2
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_F010 Homo sapiens (Human) Dyschromatosis symmetrica hereditaria Population: Japanese. Finite cell line Female BioSample:SAMN03472400,
JCRB:JCRB3001,
JCRB:KURB2099,
Wikidata:Q54828675
CVCL_F010 2026-08-15 04:26:09 0
DD0014
 
Resource Report
Resource Website
RRID:CVCL_8U31 Homo sapiens (Human) Fragile X syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:90012301,
Wikidata:Q54828709
CVCL_8U31 2026-08-15 04:26:10 0
DD0021
 
Resource Report
Resource Website
RRID:CVCL_8U35 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:90042701,
Wikidata:Q54828713
CVCL_8U35 2026-08-15 04:26:10 0
Dch4F
 
Resource Report
Resource Website
Possibly Discontinued
JCRB Cat# KURB2101, RRID:CVCL_F012 Homo sapiens (Human) Dyschromatosis symmetrica hereditaria Population: Japanese. Finite cell line Male JCRB KURB2101 BioSample:SAMN03472404,
JCRB:JCRB3004,
JCRB:KURB2101,
Wikidata:Q54828677
CVCL_F012 2026-08-15 04:26:09 0
DCH002
 
Resource Report
Resource Website
ECACC Cat# 94082282, RRID:CVCL_E547 Homo sapiens (Human) Population: Southeast Asian; Thai., Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel. PMID:8307784
PMID:30844424
Transformed cell line Female DCH 002, DCH-002, Thai-DCH002 ECACC 94082282 dbMHC:48745,
ECACC:94082282,
IHW:IHW09182,
IPD-IMGT/HLA:11724,
Wikidata:Q54828657
CVCL_E547 2026-08-15 04:26:10 0
DD0007
 
Resource Report
Resource Website
RRID:CVCL_8U29 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:90041701,
Wikidata:Q54828707
CVCL_8U29 2026-08-15 04:26:10 0
DD-1 [Mouse hybridoma against TCDD]
 
Resource Report
Resource Website
RRID:CVCL_J826 Mus musculus (Mouse) Group: Patented cell line. Hybridoma ATCC:HB-9741,
Wikidata:Q54828695
cvcl_2199 CVCL_J826 2026-08-15 04:26:09 0
DCE2.2
 
Resource Report
Resource Website
RRID:CVCL_HM07 Homo sapiens (Human) Donor information: Established from monozygotic twin of DCE2.1 (Cellosaurus=CVCL_HM06). PMID:18435749 Transformed cell line Female DisCordant Epilepsy 2.2 GEO:GSM181374,
Wikidata:Q54828648
CVCL_HM07 2026-08-15 04:26:08 0
DD0001
 
Resource Report
Resource Website
ECACC Cat# 89030312, RRID:CVCL_8U26 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 89030312 ECACC:89030312,
Wikidata:Q54828704
CVCL_8U26 2026-08-15 04:26:10 0
DD0029
 
Resource Report
Resource Website
ECACC Cat# 90080203, RRID:CVCL_8U40 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 90080203 ECACC:90080203,
Wikidata:Q54828718
CVCL_8U40 2026-08-15 04:26:11 0

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