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On page 461 showing 9201 ~ 9220 out of 19,458 results
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  • RRID:CVCL_U701

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_U701

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

Proper citation: Coriell Cat# AG01437, RRID:CVCL_U701 Copy   


  • RRID:CVCL_8B48

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B48

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_8B48 Copy   


  • RRID:CVCL_8B53

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B53

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_8B53 Copy   


  • RRID:CVCL_V551

Possibly Discontinued Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_V551

Organism: Homo sapiens (Human)
Disease: Progeria
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_V551 Copy   


  • RRID:CVCL_JE20

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JE20

Organism: Homo sapiens (Human)
Disease: Oculocerebrorenal syndrome
Category: Finite cell line
Comments:

Proper citation: Coriell Cat# AG01756, RRID:CVCL_JE20 Copy   


  • RRID:CVCL_JE42

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JE42

Organism: Homo sapiens (Human)
Disease: Kidney Wilms tumor
Category: Finite cell line
Comments: Donor information: Established from the irradiated skin of a nephroblastoma patient.

Proper citation: RRID:CVCL_JE42 Copy   


  • RRID:CVCL_JE21

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JE21

Organism: Homo sapiens (Human)
Disease: Cowden syndrome
Category: Finite cell line
Comments:

Proper citation: Coriell Cat# AG01964, RRID:CVCL_JE21 Copy   


  • RRID:CVCL_JE27

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JE27

Organism: Homo sapiens (Human)
Disease: Progeria
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_JE27 Copy   


  • RRID:CVCL_8B51

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B51

Organism: Homo sapiens (Human)
Disease: Alagille syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 90081517, RRID:CVCL_8B51 Copy   


  • RRID:CVCL_JE37

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JE37

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: African American.

Proper citation: Coriell Cat# AG01485, RRID:CVCL_JE37 Copy   


  • RRID:CVCL_8B52

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B52

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 90082301, RRID:CVCL_8B52 Copy   


  • RRID:CVCL_JE41

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JE41

Organism: Homo sapiens (Human)
Disease: Retinoblastoma
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_JE41 Copy   


  • RRID:CVCL_D101

Contaminated Discontinued

https://web.expasy.org/cellosaurus/CVCL_D101

Organism: Homo sapiens (Human)
Disease: Childhood T acute lymphoblastic leukemia
Category: Cancer cell line
Comments: Population: Caucasian., Problematic cell line: Contaminated. Shown to be a CCRF-CEM derivative (PubMed=12592342; PubMed=20143388). Originally thought to originates from the bone marrow of a patient suffering from neuroblastoma that evolved into a Hodgkin lymphoma.., Group: Patented cell line.

Proper citation: RRID:CVCL_D101 Copy   


  • RRID:CVCL_JE28

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JE28

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: South American (Brazil, Guyana, Venezuela).

Proper citation: RRID:CVCL_JE28 Copy   


  • RRID:CVCL_8B50

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B50

Organism: Homo sapiens (Human)
Disease: Alagille syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_8B50 Copy   


  • RRID:CVCL_8B50

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B50

Organism: Homo sapiens (Human)
Disease: Alagille syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 90081516, RRID:CVCL_8B50 Copy   


  • RRID:CVCL_JE28

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JE28

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: South American (Brazil, Guyana, Venezuela).

Proper citation: Coriell Cat# AG01839, RRID:CVCL_JE28 Copy   


  • RRID:CVCL_8B47

Discontinued

https://web.expasy.org/cellosaurus/CVCL_8B47

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 90052207, RRID:CVCL_8B47 Copy   


  • RRID:CVCL_W842

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_W842

Organism: Homo sapiens (Human)
Disease: Progeria
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_W842 Copy   


  • RRID:CVCL_A2KS

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_A2KS

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

Proper citation: RRID:CVCL_A2KS Copy   



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