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On page 94 showing 1861 ~ 1880 out of 95,747 results
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  • RRID:CVCL_7345

Discontinued

https://web.expasy.org/cellosaurus/CVCL_7345

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: Coriell Cat# GM17217, RRID:CVCL_7345 Copy   


  • RRID:CVCL_M989

https://web.expasy.org/cellosaurus/CVCL_M989

Organism: Homo sapiens (Human)
Disease: Ataxia with isolated vitamin E deficiency
Category: Finite cell line
Comments: Population: Mexican., Part of: Human variation panel.

Proper citation: RRID:CVCL_M989 Copy   


  • RRID:CVCL_L967

Discontinued

https://web.expasy.org/cellosaurus/CVCL_L967

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

Proper citation: Coriell Cat# GM01930, RRID:CVCL_L967 Copy   


  • RRID:CVCL_4E25

https://web.expasy.org/cellosaurus/CVCL_4E25

Organism: Homo sapiens (Human)
Disease: Sea-blue histiocyte syndrome
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM01912, RRID:CVCL_4E25 Copy   


  • RRID:CVCL_JD67

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JD67

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

Proper citation: RRID:CVCL_JD67 Copy   


  • RRID:CVCL_V466

https://web.expasy.org/cellosaurus/CVCL_V466

Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XX,i(21)(qter->q10::q10->qter) [13]; 46,XX [87] (Coriell=GM02058)., Population: Jewish; Ashkenazi.

Proper citation: Coriell Cat# GM02058, RRID:CVCL_V466 Copy   


  • RRID:CVCL_U703

https://web.expasy.org/cellosaurus/CVCL_U703

Organism: Homo sapiens (Human)
Disease: Bloom syndrome
Category: Finite cell line
Comments: Donor information: From Bloom Syndrome Registry patient 53(StAs) (BSR53)., Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_U703 Copy   


  • RRID:CVCL_1H41

https://web.expasy.org/cellosaurus/CVCL_1H41

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

Proper citation: RRID:CVCL_1H41 Copy   


  • RRID:CVCL_M990

https://web.expasy.org/cellosaurus/CVCL_M990

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Arab., Part of: Human variation panel.

Proper citation: RRID:CVCL_M990 Copy   


  • RRID:CVCL_H177

https://web.expasy.org/cellosaurus/CVCL_H177

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

Proper citation: RRID:CVCL_H177 Copy   


  • RRID:CVCL_CW70

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_CW70

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

Proper citation: RRID:CVCL_CW70 Copy   


  • RRID:CVCL_V030

https://web.expasy.org/cellosaurus/CVCL_V030

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

Proper citation: RRID:CVCL_V030 Copy   


  • RRID:CVCL_1H40

https://web.expasy.org/cellosaurus/CVCL_1H40

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Donor information: At sampling donor was not affected with Huntington disease but at 50% risk for disease., Population: Caucasian.

Proper citation: Coriell Cat# GM02078, RRID:CVCL_1H40 Copy   


  • RRID:CVCL_1N60

https://web.expasy.org/cellosaurus/CVCL_1N60

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(6;7)(6pter->6q27::7q22->7qter;7pter->7q22::6q27->6qter) (Coriell=GM02068)., Population: Caucasian.

Proper citation: Coriell Cat# GM02068, RRID:CVCL_1N60 Copy   


  • RRID:CVCL_F593

https://web.expasy.org/cellosaurus/CVCL_F593

Organism: Homo sapiens (Human)
Disease: Fanconi anemia
Category: Finite cell line
Comments: Population: Arab.

Proper citation: RRID:CVCL_F593 Copy   


  • RRID:CVCL_1H40

https://web.expasy.org/cellosaurus/CVCL_1H40

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Donor information: At sampling donor was not affected with Huntington disease but at 50% risk for disease., Population: Caucasian.

Proper citation: RRID:CVCL_1H40 Copy   


  • RRID:CVCL_X260

https://web.expasy.org/cellosaurus/CVCL_X260

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;Y)(q11;q11) (PubMed=10377420)., Population: Caucasian.

Proper citation: Coriell Cat# GM02103, RRID:CVCL_X260 Copy   


  • RRID:CVCL_F593

https://web.expasy.org/cellosaurus/CVCL_F593

Organism: Homo sapiens (Human)
Disease: Fanconi anemia
Category: Finite cell line
Comments: Population: Arab.

Proper citation: Coriell Cat# GM02053, RRID:CVCL_F593 Copy   


  • RRID:CVCL_M991

https://web.expasy.org/cellosaurus/CVCL_M991

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Arab., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_M991 Copy   


  • RRID:CVCL_1H42

https://web.expasy.org/cellosaurus/CVCL_1H42

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

Proper citation: Coriell Cat# GM02080, RRID:CVCL_1H42 Copy   



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