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On page 78 showing 1541 ~ 1560 out of 10,882 results
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https://web.expasy.org/cellosaurus/CVCL_M572

Organism: Homo sapiens (Human)
Disease: AIDS-related non-Hodgkin lymphoma
Category: Cancer cell line

Proper citation: RRID:CVCL_M572 Copy   


  • RRID:CVCL_4221

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_4221

Organism: Homo sapiens (Human)
Disease: Primary effusion lymphoma
Category: Cancer cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_4221 Copy   


  • RRID:CVCL_JQ59

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_JQ59

Organism: Homo sapiens (Human)
Category: Spontaneously immortalized cell line

Proper citation: RRID:CVCL_JQ59 Copy   


  • RRID:CVCL_4362

    This resource has 1+ mentions.

Misidentified Discontinued Discontinued

https://web.expasy.org/cellosaurus/CVCL_4362

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Karyotypic information: Near triploid with the modal number of 67 chromosomes (ATCC=HTB-124)., Virology: Contains 2 copies of the SV40 genome, one complete the other incomplete tandemly integrated in the cell line genome., Part of: JWGray breast cancer cell line panel., Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE)., Problematic cell line: Misidentified. Presence of a Y chromosome in cell line that was thought to be of female origin (PubMed=16643607; PubMed=20143388). Originally thought to originate from a casein-producing breast cell line from a 27 year old Caucasian woman. In addition contains SV40 genomic sequence while the cell line was deemed to be spontaneously immortalized..

Proper citation: ATCC Cat# HTB-124, RRID:CVCL_4362 Copy   


  • RRID:CVCL_X491

    This resource has 10+ mentions.

https://web.expasy.org/cellosaurus/CVCL_X491

Organism: Homo sapiens (Human)
Category: Telomerase immortalized cell line
Comments: Part of: Human Protein Atlas, Cell Atlas panel.

Proper citation: RRID:CVCL_X491 Copy   


  • RRID:CVCL_4362

    This resource has 1+ mentions.

Misidentified Discontinued Discontinued

https://web.expasy.org/cellosaurus/CVCL_4362

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Karyotypic information: Near triploid with the modal number of 67 chromosomes (ATCC=HTB-124)., Virology: Contains 2 copies of the SV40 genome, one complete the other incomplete tandemly integrated in the cell line genome., Part of: JWGray breast cancer cell line panel., Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE)., Problematic cell line: Misidentified. Presence of a Y chromosome in cell line that was thought to be of female origin (PubMed=16643607; PubMed=20143388). Originally thought to originate from a casein-producing breast cell line from a 27 year old Caucasian woman. In addition contains SV40 genomic sequence while the cell line was deemed to be spontaneously immortalized..

Proper citation: RRID:CVCL_4362 Copy   


  • RRID:CVCL_Z631

    This resource has 1+ mentions.

Possibly Contaminated Possibly Contaminated Discontinued

https://web.expasy.org/cellosaurus/CVCL_Z631

Organism: Homo sapiens (Human)
Disease: Hepatoblastoma
Category: Cancer cell line
Comments: Population: Caucasian., Problematic cell line: Possibly contaminated. Indicated (PubMed=24532842) to have a near genetic identity with Hep-G2 cells. But they are functionally different from Hep-G2 cells since they support sporozoite invasion and liver stage exoerythrocytic development of Plasmodium falciparum and Plasmodium vivax. But STR profile from BEI Resources is identical to that of Hep-G2. Originally thought to originate from the spontaneous immortalization of a normal liver tissue of an hepatoma patient.., Group: Patented cell line., Group: Malaria research cell line.

Proper citation: RRID:CVCL_Z631 Copy   


  • RRID:CVCL_1H73

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_1H73

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM03868, RRID:CVCL_1H73 Copy   


  • RRID:CVCL_T820

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_T820

Organism: Homo sapiens (Human)
Disease: Friedreich ataxia
Category: Finite cell line
Comments: Caution: Indicated by Coriell to have 420 and 541 GAA repeats., Population: Caucasian.

Proper citation: RRID:CVCL_T820 Copy   


  • RRID:CVCL_V473

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_V473

Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_V473 Copy   


  • RRID:CVCL_7413

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7413

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Donor information: Established from monozygotic twin of GM04505 (Cellosaurus=CVCL_7412)., Population: Caucasian.

Proper citation: RRID:CVCL_7413 Copy   


  • RRID:CVCL_7413

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7413

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Donor information: Established from monozygotic twin of GM04505 (Cellosaurus=CVCL_7412)., Population: Caucasian.

Proper citation: Coriell Cat# GM04506, RRID:CVCL_7413 Copy   


  • RRID:CVCL_V475

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_V475

Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM04616, RRID:CVCL_V475 Copy   


  • RRID:CVCL_X310

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_X310

Organism: Homo sapiens (Human)
Category: Finite cell line

Proper citation: Coriell Cat# GM04626, RRID:CVCL_X310 Copy   


  • RRID:CVCL_X310

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_X310

Organism: Homo sapiens (Human)
Category: Finite cell line

Proper citation: RRID:CVCL_X310 Copy   


  • RRID:CVCL_V475

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_V475

Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_V475 Copy   


  • RRID:CVCL_AX78

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_AX78

Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_AX78 Copy   


  • RRID:CVCL_AX78

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_AX78

Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM05131, RRID:CVCL_AX78 Copy   


  • RRID:CVCL_7432

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7432

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Latino or Hispanic.

Proper citation: RRID:CVCL_7432 Copy   


  • RRID:CVCL_7434

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7434

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_7434 Copy   



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