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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
BLi0251
 
Resource Report
Resource Website
ECACC Cat# 15042404, RRID:CVCL_VA66 Homo sapiens (Human) Amyotrophic lateral sclerosis Part of: Motor Neurone Disease (MND) collection. Transformed cell line Female ECACC 15042404 ECACC:15042404,
Wikidata:Q54797351
CVCL_VA66 2026-07-25 05:26:53 0
BLi0083
 
Resource Report
Resource Website
ECACC Cat# 15092907, RRID:CVCL_VA60 Homo sapiens (Human) Part of: Motor Neurone Disease (MND) collection. Transformed cell line Female ECACC 15092907 ECACC:15092907,
Wikidata:Q54797340
CVCL_VA60 2026-07-25 05:26:53 0
BLi0097
 
Resource Report
Resource Website
ECACC Cat# 15102929, RRID:CVCL_VA61 Homo sapiens (Human) Part of: Motor Neurone Disease (MND) collection. Transformed cell line Male ECACC 15102929 ECACC:15102929,
Wikidata:Q54797341
CVCL_VA61 2026-07-25 05:26:53 0
BLi0265
 
Resource Report
Resource Website
ECACC Cat# 15042405, RRID:CVCL_VA68 Homo sapiens (Human) Amyotrophic lateral sclerosis Part of: Motor Neurone Disease (MND) collection. Transformed cell line Male ECACC 15042405 ECACC:15042405,
Wikidata:Q54797354
CVCL_VA68 2026-07-25 05:26:56 0
BM21
 
Resource Report
Resource Website
ECACC Cat# 88052043, RRID:CVCL_E488 Homo sapiens (Human) Population: Caucasian; German/Italian., Part of: 10th International Histocompatibility Workshop (10IHW) cell line panel. PMID:8813743
PMID:28360230
PMID:29171935
PMID:30844424
Transformed cell line Male BM 21 ECACC 88052043 dbMHC:48504,
ECACC:88052043,
IHW:IHW09043,
IPD-IMGT/HLA:10322,
Wikidata:Q54797472
CVCL_E488 2026-07-25 05:26:58 0
BM9
 
Resource Report
Resource Website
ECACC Cat# 88052086, RRID:CVCL_E489 Homo sapiens (Human) Part of: 10th International Histocompatibility Workshop (10IHW) cell line panel. PMID:8813743
PMID:28360230
PMID:29171935
Transformed cell line Female BM 9, BM09 ECACC 88052086 EFO:EFO_0022641,
dbMHC:48505,
ECACC:88052086,
IHW:IHW09068,
IPD-IMGT/HLA:11619,
Wikidata:Q54797489
CVCL_E489 2026-07-25 05:26:55 0
BME/CTVM6
 
Resource Report
Resource Website
Possibly Discontinued
ECACC Cat# 94022803, RRID:CVCL_Z150 Rhipicephalus microplus (Cattle tick) Group: Tick cell line. PMID:15053931
PMID:17662657
PMID:20388200
PMID:21955214
PMID:22743047
PMID:27484910
PMID:29886187
PMID:32158404
Spontaneously immortalized cell line Sex unspecified BME/CTVM 6 ECACC 94022803 ECACC:94022803,
Wikidata:Q54797573
CVCL_Z150 2026-07-25 05:26:55 0
BO0338
 
Resource Report
Resource Website
ECACC Cat# 92032601, RRID:CVCL_8S95 Homo sapiens (Human) Karyotypic information: 46,XY,t(2;4)(11;14) (ECACC=92032601)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92032601 ECACC:92032601,
Wikidata:Q54797725
CVCL_8S95 2026-07-25 05:26:57 0
BO0306
 
Resource Report
Resource Website
Possibly Discontinued
ECACC Cat# 91111305, RRID:CVCL_GZ18 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91111305 ECACC:91111305,
Wikidata:Q54797694
CVCL_GZ18 2026-07-25 05:27:01 0
BO0362
 
Resource Report
Resource Website
ECACC Cat# 92052010, RRID:CVCL_8S96 Homo sapiens (Human) Karyotypic information: 46,XX,?t(2;12)(q32;q15),inv(6)(p21.1;p23) (ECACC=92052010)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92052010 ECACC:92052010,
Wikidata:Q54797727
CVCL_8S96 2026-07-25 05:27:01 0
BO0312
 
Resource Report
Resource Website
ECACC Cat# 91121001, RRID:CVCL_8S92 Homo sapiens (Human) Turner syndrome Karyotypic information: 46,XXq- (ECACC=91121001)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91121001 ECACC:91121001,
Wikidata:Q54797696
CVCL_8S92 2026-07-25 05:26:57 0
BO0329
 
Resource Report
Resource Website
ECACC Cat# 92022002, RRID:CVCL_8S93 Homo sapiens (Human) Hypogonadism Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92022002 ECACC:92022002,
Wikidata:Q54797698
CVCL_8S93 2026-07-25 05:27:01 0
BO0737
 
Resource Report
Resource Website
ECACC Cat# 93071404, RRID:CVCL_8T27 Homo sapiens (Human) Karyotypic information: 46,XY,-22,+der(22)(T) (ECACC=93071404)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93071404 ECACC:93071404,
Wikidata:Q54797776
CVCL_8T27 2026-07-25 05:26:58 0
BO0574
 
Resource Report
Resource Website
ECACC Cat# 93020207, RRID:CVCL_8T12 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93020207 ECACC:93020207,
Wikidata:Q54797752
CVCL_8T12 2026-07-25 05:26:58 0
BO0392
 
Resource Report
Resource Website
ECACC Cat# 92062610, RRID:CVCL_8T02 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92062610 ECACC:92062610,
Wikidata:Q54797736
CVCL_8T02 2026-07-25 05:27:01 0
BO0389
 
Resource Report
Resource Website
ECACC Cat# 92061815, RRID:CVCL_8T01 Homo sapiens (Human) Turner syndrome Karyotypic information: 46,X,del(X)(qter-cen) (ECACC=92061815)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92061815 ECACC:92061815,
Wikidata:Q54797734
CVCL_8T01 2026-07-25 05:26:57 0
BO0770
 
Resource Report
Resource Website
ECACC Cat# 93081915, RRID:CVCL_8T31 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93081915 ECACC:93081915,
Wikidata:Q54797784
CVCL_8T31 2026-07-25 05:26:58 0
BO0790
 
Resource Report
Resource Website
ECACC Cat# 93101104, RRID:CVCL_8T34 Homo sapiens (Human) Developmental delay Karyotypic information: 47,XY,+marker (ECACC=93101104)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93101104 ECACC:93101104,
Wikidata:Q54797812
CVCL_8T34 2026-07-25 05:26:58 0
BO0401
 
Resource Report
Resource Website
ECACC Cat# 92070702, RRID:CVCL_8T04 Homo sapiens (Human) Fragile X syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92070702 ECACC:92070702,
Wikidata:Q54797738
CVCL_8T04 2026-07-25 05:26:57 0
BO0663
 
Resource Report
Resource Website
ECACC Cat# 93050613, RRID:CVCL_8T18 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93050613 ECACC:93050613,
Wikidata:Q54797761
CVCL_8T18 2026-07-25 05:26:58 0

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