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95,747 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
HH0012
 
Resource Report
Resource Website
RRID:CVCL_8W67 Homo sapiens (Human) Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:89030650,
Wikidata:Q54887351
CVCL_8W67 2026-09-05 11:04:37 0
HGMLBV065
 
Resource Report
Resource Website
RRID:CVCL_1Z42 Homo sapiens (Human) Part of: Progeria Research Foundation cell lines. Transformed cell line Female Wikidata:Q54887301 CVCL_1Z42 2026-09-05 11:04:36 0
HGRT
 
Resource Report
Resource Website
RCB Cat# RCB0966, RRID:CVCL_H733 Homo sapiens (Human) Mature gastric teratoma Population: Japanese. Finite cell line Female RCB RCB0966 CLO:CLO_0050118,
BioSample:SAMN03472190,
FANTOM5_SSTAR:10694-109G1,
RCB:RCB0966,
Wikidata:Q54887323
CVCL_H733 2026-09-05 11:04:36 0
HH0030
 
Resource Report
Resource Website
RRID:CVCL_8W79 Homo sapiens (Human) Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:89030619,
Wikidata:Q54887365
CVCL_8W79 2026-09-05 11:04:37 0
HGRT
 
Resource Report
Resource Website
RRID:CVCL_H733 Homo sapiens (Human) Mature gastric teratoma Population: Japanese. Finite cell line Female CLO:CLO_0050118,
BioSample:SAMN03472190,
FANTOM5_SSTAR:10694-109G1,
RCB:RCB0966,
Wikidata:Q54887323
CVCL_H733 2026-09-05 11:04:36 0
HGSLBV353
 
Resource Report
Resource Website
RRID:CVCL_1Z73 Homo sapiens (Human) Part of: Progeria Research Foundation cell lines. Transformed cell line Female Wikidata:Q54887328 CVCL_1Z73 2026-09-05 11:04:36 0
HH0009
 
Resource Report
Resource Website
RRID:CVCL_8W64 Homo sapiens (Human) Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:89030659,
Wikidata:Q54887348
CVCL_8W64 2026-09-05 11:04:37 0
HGMLBV058
 
Resource Report
Resource Website
RRID:CVCL_2A21 Homo sapiens (Human) Miscellaneous: Cell line no longer available., Part of: Progeria Research Foundation cell lines. PMID:12714972 Transformed cell line Female Wikidata:Q54887300 CVCL_2A21 2026-09-05 11:04:36 0
HGMLBV133
 
Resource Report
Resource Website
RRID:CVCL_1Z58 Homo sapiens (Human) Part of: Progeria Research Foundation cell lines. Transformed cell line Female Wikidata:Q54887307 CVCL_1Z58 2026-09-05 11:04:36 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 2026-09-05 11:04:37 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 2026-09-05 11:04:39 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 2026-09-05 11:04:38 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 2026-09-05 11:04:38 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 2026-09-05 11:04:38 0
HH0093
 
Resource Report
Resource Website
RRID:CVCL_8W99 Homo sapiens (Human) Trisomy 13 Karyotypic information: 47,XX,+13 (ECACC=89041121)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:89041121,
Wikidata:Q54887386
CVCL_8W99 2026-09-05 11:04:38 0
HH01
 
Resource Report
Resource Website
RRID:CVCL_4Z97 Homo sapiens (Human) PMID:7514562
PMID:8095227
Spontaneously immortalized cell line Female Wikidata:Q54887391 CVCL_4Z97 2026-09-05 11:04:38 0
HH0061
 
Resource Report
Resource Website
RRID:CVCL_8W91 Homo sapiens (Human) Karyotypic information: 46,XX,dir ins(2;18)(q2.1;q11.2 q21.3) (ECACC=89030272)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:89030272,
Wikidata:Q54887378
CVCL_8W91 2026-09-05 11:04:38 0
HH0102
 
Resource Report
Resource Website
RRID:CVCL_8X04 Homo sapiens (Human) Karyotypic information: 48,XX,+i(Yq)+i(Yq) (ECACC=89041144)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:89041144,
Wikidata:Q54887392
CVCL_8X04 2026-09-05 11:04:38 0
HH0108
 
Resource Report
Resource Website
ECACC Cat# 89041153, RRID:CVCL_8X10 Homo sapiens (Human) Karyotypic information: 46,XX,t(1;14)(q21;q32) (ECACC=89041153)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 89041153 ECACC:89041153,
Wikidata:Q54887399
CVCL_8X10 2026-09-05 11:04:38 0
HH0110
 
Resource Report
Resource Website
RRID:CVCL_8X11 Homo sapiens (Human) Karyotypic information: 46,XX; 47,XX,+2; 47,XX,+21 (ECACC=89042116)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:89042116,
Wikidata:Q54887400
CVCL_8X11 2026-09-05 11:04:38 0

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