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On page 383 showing 7641 ~ 7660 out of 236,573 results
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  • RRID:CVCL_N017

https://web.expasy.org/cellosaurus/CVCL_N017

Organism: Homo sapiens (Human)
Disease: Zellweger syndrome
Category: Finite cell line
Comments: Population: Caucasian; Iberian., Part of: Human variation panel.

Proper citation: Coriell Cat# GM17092, RRID:CVCL_N017 Copy   


  • RRID:CVCL_2T04

https://web.expasy.org/cellosaurus/CVCL_2T04

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(2;14)(2qter->2p23::14q32->14qter;14pter->14q32::2p23->2pter) (Coriell=GM04410)., Population: Caucasian.

Proper citation: Coriell Cat# GM04410, RRID:CVCL_2T04 Copy   


  • RRID:CVCL_AI34

https://web.expasy.org/cellosaurus/CVCL_AI34

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.

Proper citation: RRID:CVCL_AI34 Copy   


  • RRID:CVCL_V565

https://web.expasy.org/cellosaurus/CVCL_V565

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection.

Proper citation: Coriell Cat# GM04284, RRID:CVCL_V565 Copy   


  • RRID:CVCL_GS63

https://web.expasy.org/cellosaurus/CVCL_GS63

Organism: Homo sapiens (Human)
Disease: Tyrosinemia type II
Category: Finite cell line
Comments: Population: Native North American.

Proper citation: RRID:CVCL_GS63 Copy   


  • RRID:CVCL_2Z50

https://web.expasy.org/cellosaurus/CVCL_2Z50

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

Proper citation: RRID:CVCL_2Z50 Copy   


  • RRID:CVCL_AI32

https://web.expasy.org/cellosaurus/CVCL_AI32

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.

Proper citation: Coriell Cat# GM04420, RRID:CVCL_AI32 Copy   


  • RRID:CVCL_Y867

https://web.expasy.org/cellosaurus/CVCL_Y867

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection.

Proper citation: RRID:CVCL_Y867 Copy   


  • RRID:CVCL_9Y77

https://web.expasy.org/cellosaurus/CVCL_9Y77

Organism: Homo sapiens (Human)
Disease: Albright's hereditary osteodystrophy
Category: Transformed cell line

Proper citation: RRID:CVCL_9Y77 Copy   


  • RRID:CVCL_Y867

https://web.expasy.org/cellosaurus/CVCL_Y867

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection.

Proper citation: Coriell Cat# GM04285, RRID:CVCL_Y867 Copy   


  • RRID:CVCL_0M32

https://web.expasy.org/cellosaurus/CVCL_0M32

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

Proper citation: RRID:CVCL_0M32 Copy   


  • RRID:CVCL_W622

https://web.expasy.org/cellosaurus/CVCL_W622

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

Proper citation: Coriell Cat# GM04375, RRID:CVCL_W622 Copy   


  • RRID:CVCL_0R33

https://web.expasy.org/cellosaurus/CVCL_0R33

Organism: Homo sapiens (Human)
Disease: Gaucher disease
Category: Finite cell line
Comments: Population: African American., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_0R33 Copy   


  • RRID:CVCL_GT50

https://web.expasy.org/cellosaurus/CVCL_GT50

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

Proper citation: RRID:CVCL_GT50 Copy   


  • RRID:CVCL_5M95

https://web.expasy.org/cellosaurus/CVCL_5M95

Organism: Homo sapiens (Human)
Disease: Duchenne muscular dystrophy
Category: Finite cell line
Comments: Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_5M95 Copy   


  • RRID:CVCL_H153

https://web.expasy.org/cellosaurus/CVCL_H153

Organism: Mus musculus (Mouse)
Category: Hybridoma

Proper citation: Coriell Cat# GM04280, RRID:CVCL_H153 Copy   


  • RRID:CVCL_CZ83

https://web.expasy.org/cellosaurus/CVCL_CZ83

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

Proper citation: RRID:CVCL_CZ83 Copy   


  • RRID:CVCL_9Y78

https://web.expasy.org/cellosaurus/CVCL_9Y78

Organism: Homo sapiens (Human)
Disease: Albright's hereditary osteodystrophy
Category: Transformed cell line

Proper citation: RRID:CVCL_9Y78 Copy   


  • RRID:CVCL_Y868

https://web.expasy.org/cellosaurus/CVCL_Y868

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection.

Proper citation: RRID:CVCL_Y868 Copy   


  • RRID:CVCL_0M26

https://web.expasy.org/cellosaurus/CVCL_0M26

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

Proper citation: RRID:CVCL_0M26 Copy   



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