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On page 218 showing 4341 ~ 4360 out of 236,573 results
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  • RRID:CVCL_X135

https://web.expasy.org/cellosaurus/CVCL_X135

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

Proper citation: Coriell Cat# GM05011, RRID:CVCL_X135 Copy   


  • RRID:CVCL_5N00

https://web.expasy.org/cellosaurus/CVCL_5N00

Organism: Homo sapiens (Human)
Disease: Dyggve-Melchior-Clausen syndrome
Category: Finite cell line
Comments: Population: Lebanese.

Proper citation: RRID:CVCL_5N00 Copy   


  • RRID:CVCL_GQ36

https://web.expasy.org/cellosaurus/CVCL_GQ36

Organism: Homo sapiens (Human)
Disease: Bipolar disorder
Category: Transformed cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_GQ36 Copy   


  • RRID:CVCL_1I76

https://web.expasy.org/cellosaurus/CVCL_1I76

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

Proper citation: RRID:CVCL_1I76 Copy   


  • RRID:CVCL_GQ32

https://web.expasy.org/cellosaurus/CVCL_GQ32

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

Proper citation: RRID:CVCL_GQ32 Copy   


  • RRID:CVCL_AB35

https://web.expasy.org/cellosaurus/CVCL_AB35

Organism: Homo sapiens (Human)
Disease: Triploidy syndrome
Category: Finite cell line
Comments: Karyotypic information: 69,XXX (Coriell=GM04939)., Population: Caucasian.

Proper citation: RRID:CVCL_AB35 Copy   


  • RRID:CVCL_AK98

https://web.expasy.org/cellosaurus/CVCL_AK98

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

Proper citation: Coriell Cat# GM05058, RRID:CVCL_AK98 Copy   


  • RRID:CVCL_AA43

https://web.expasy.org/cellosaurus/CVCL_AA43

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

Proper citation: RRID:CVCL_AA43 Copy   


  • RRID:CVCL_8521

https://web.expasy.org/cellosaurus/CVCL_8521

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

Proper citation: RRID:CVCL_8521 Copy   


  • RRID:CVCL_GQ28

https://web.expasy.org/cellosaurus/CVCL_GQ28

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

Proper citation: Coriell Cat# GM04942, RRID:CVCL_GQ28 Copy   


  • RRID:CVCL_AL00

https://web.expasy.org/cellosaurus/CVCL_AL00

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

Proper citation: Coriell Cat# GM05060, RRID:CVCL_AL00 Copy   


  • RRID:CVCL_AA47

https://web.expasy.org/cellosaurus/CVCL_AA47

Organism: Homo sapiens (Human)
Disease: Familial dysautonomia
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_AA47 Copy   


  • RRID:CVCL_GQ28

https://web.expasy.org/cellosaurus/CVCL_GQ28

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

Proper citation: RRID:CVCL_GQ28 Copy   


  • RRID:CVCL_9W98

https://web.expasy.org/cellosaurus/CVCL_9W98

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

Proper citation: RRID:CVCL_9W98 Copy   


  • RRID:CVCL_N036

https://web.expasy.org/cellosaurus/CVCL_N036

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: African American., Part of: Human variation panel.

Proper citation: Coriell Cat# GM17158, RRID:CVCL_N036 Copy   


  • RRID:CVCL_7416

https://web.expasy.org/cellosaurus/CVCL_7416

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

Proper citation: Coriell Cat# GM05048, RRID:CVCL_7416 Copy   


  • RRID:CVCL_GQ32

https://web.expasy.org/cellosaurus/CVCL_GQ32

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

Proper citation: Coriell Cat# GM04952, RRID:CVCL_GQ32 Copy   


  • RRID:CVCL_AA51

https://web.expasy.org/cellosaurus/CVCL_AA51

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_AA51 Copy   


  • RRID:CVCL_5N01

https://web.expasy.org/cellosaurus/CVCL_5N01

Organism: Homo sapiens (Human)
Disease: Duchenne muscular dystrophy
Category: Transformed cell line

Proper citation: RRID:CVCL_5N01 Copy   


  • RRID:CVCL_V479

https://web.expasy.org/cellosaurus/CVCL_V479

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

Proper citation: Coriell Cat# GM04965, RRID:CVCL_V479 Copy   



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