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On page 237 showing 4721 ~ 4740 out of 256,031 results
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  • RRID:CVCL_M980

https://web.expasy.org/cellosaurus/CVCL_M980

Organism: Homo sapiens (Human)
Disease: Metachromatic leukodystrophy
Category: Transformed cell line
Comments: Population: Puerto Rican., Part of: Human variation panel.

Proper citation: RRID:CVCL_M980 Copy   


  • RRID:CVCL_4D80

https://web.expasy.org/cellosaurus/CVCL_4D80

Organism: Homo sapiens (Human)
Disease: Supernumerary circular chromosome
Category: Finite cell line
Comments: Karyotypic information: 46,XX,r(18) [39]; 45,XX,-18 [11] (Coriell=GM01118)., Population: Mexican.

Proper citation: Coriell Cat# GM01118, RRID:CVCL_4D80 Copy   


  • RRID:CVCL_V531

https://web.expasy.org/cellosaurus/CVCL_V531

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

Proper citation: Coriell Cat# GM01053, RRID:CVCL_V531 Copy   


  • RRID:CVCL_CV39

https://web.expasy.org/cellosaurus/CVCL_CV39

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

Proper citation: RRID:CVCL_CV39 Copy   


  • RRID:CVCL_X079

https://web.expasy.org/cellosaurus/CVCL_X079

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

Proper citation: Coriell Cat# GM01059, RRID:CVCL_X079 Copy   


  • RRID:CVCL_V038

https://web.expasy.org/cellosaurus/CVCL_V038

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

Proper citation: Coriell Cat# GM01085, RRID:CVCL_V038 Copy   


  • RRID:CVCL_CX40

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_CX40

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

Proper citation: Coriell Cat# GM00994, RRID:CVCL_CX40 Copy   


  • RRID:CVCL_M981

https://web.expasy.org/cellosaurus/CVCL_M981

Organism: Homo sapiens (Human)
Disease: Hurler-Scheie syndrome
Category: Transformed cell line
Comments: Population: Indo Pakistani., Part of: Human variation panel.

Proper citation: RRID:CVCL_M981 Copy   


  • RRID:CVCL_0P87

https://web.expasy.org/cellosaurus/CVCL_0P87

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,(4qter->4p16::12p11->12pter;12qter->12p11::4p16->4pter) (Coriell=GM01101)., Population: Caucasian.

Proper citation: Coriell Cat# GM01101, RRID:CVCL_0P87 Copy   


  • RRID:CVCL_V036

https://web.expasy.org/cellosaurus/CVCL_V036

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

Proper citation: Coriell Cat# GM01061, RRID:CVCL_V036 Copy   


  • RRID:CVCL_V792

https://web.expasy.org/cellosaurus/CVCL_V792

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

Proper citation: RRID:CVCL_V792 Copy   


  • RRID:CVCL_GS53

https://web.expasy.org/cellosaurus/CVCL_GS53

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

Proper citation: RRID:CVCL_GS53 Copy   


  • RRID:CVCL_H964

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_H964

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

Proper citation: RRID:CVCL_H964 Copy   


  • RRID:CVCL_CX37

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_CX37

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

Proper citation: Coriell Cat# GM01068, RRID:CVCL_CX37 Copy   


  • RRID:CVCL_1V11

https://web.expasy.org/cellosaurus/CVCL_1V11

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

Proper citation: RRID:CVCL_1V11 Copy   


  • RRID:CVCL_6B40

https://web.expasy.org/cellosaurus/CVCL_6B40

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

Proper citation: Coriell Cat# GM01016, RRID:CVCL_6B40 Copy   


  • RRID:CVCL_V531

https://web.expasy.org/cellosaurus/CVCL_V531

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

Proper citation: RRID:CVCL_V531 Copy   


  • RRID:CVCL_V036

https://web.expasy.org/cellosaurus/CVCL_V036

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

Proper citation: RRID:CVCL_V036 Copy   


  • RRID:CVCL_DF15

https://web.expasy.org/cellosaurus/CVCL_DF15

Organism: Homo sapiens (Human)
Disease: Macular dystrophy, retinal, 1
Category: Finite cell line
Comments:

Proper citation: Coriell Cat# GM01125, RRID:CVCL_DF15 Copy   


  • RRID:CVCL_M982

https://web.expasy.org/cellosaurus/CVCL_M982

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Latino or Hispanic; Dominican., Part of: Human variation panel.

Proper citation: RRID:CVCL_M982 Copy   



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