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On page 199 showing 3961 ~ 3980 out of 256,031 results
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  • RRID:CVCL_AA94

https://web.expasy.org/cellosaurus/CVCL_AA94

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

Proper citation: RRID:CVCL_AA94 Copy   


  • RRID:CVCL_AA98

https://web.expasy.org/cellosaurus/CVCL_AA98

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

Proper citation: RRID:CVCL_AA98 Copy   


  • RRID:CVCL_GT53

https://web.expasy.org/cellosaurus/CVCL_GT53

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

Proper citation: Coriell Cat# GM09822, RRID:CVCL_GT53 Copy   


  • RRID:CVCL_GT54

https://web.expasy.org/cellosaurus/CVCL_GT54

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

Proper citation: Coriell Cat# GM09832, RRID:CVCL_GT54 Copy   


  • RRID:CVCL_AL90

https://web.expasy.org/cellosaurus/CVCL_AL90

Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.

Proper citation: RRID:CVCL_AL90 Copy   


  • RRID:CVCL_AL94

https://web.expasy.org/cellosaurus/CVCL_AL94

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.

Proper citation: RRID:CVCL_AL94 Copy   


  • RRID:CVCL_AM08

https://web.expasy.org/cellosaurus/CVCL_AM08

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.

Proper citation: RRID:CVCL_AM08 Copy   


  • RRID:CVCL_DB69

https://web.expasy.org/cellosaurus/CVCL_DB69

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

Proper citation: Coriell Cat# GM09814, RRID:CVCL_DB69 Copy   


  • RRID:CVCL_AM04

https://web.expasy.org/cellosaurus/CVCL_AM04

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.

Proper citation: RRID:CVCL_AM04 Copy   


  • RRID:CVCL_AB00

https://web.expasy.org/cellosaurus/CVCL_AB00

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

Proper citation: RRID:CVCL_AB00 Copy   


  • RRID:CVCL_DB69

https://web.expasy.org/cellosaurus/CVCL_DB69

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

Proper citation: RRID:CVCL_DB69 Copy   


  • RRID:CVCL_GT53

https://web.expasy.org/cellosaurus/CVCL_GT53

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

Proper citation: RRID:CVCL_GT53 Copy   


  • RRID:CVCL_6G79

https://web.expasy.org/cellosaurus/CVCL_6G79

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

Proper citation: RRID:CVCL_6G79 Copy   


  • RRID:CVCL_N118

https://web.expasy.org/cellosaurus/CVCL_N118

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi., Part of: Human variation panel.

Proper citation: Coriell Cat# GM17366, RRID:CVCL_N118 Copy   


  • RRID:CVCL_N119

https://web.expasy.org/cellosaurus/CVCL_N119

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

Proper citation: Coriell Cat# GM09771, RRID:CVCL_N119 Copy   


  • RRID:CVCL_AA93

https://web.expasy.org/cellosaurus/CVCL_AA93

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

Proper citation: RRID:CVCL_AA93 Copy   


  • RRID:CVCL_X474

https://web.expasy.org/cellosaurus/CVCL_X474

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

Proper citation: Coriell Cat# GM09816, RRID:CVCL_X474 Copy   


  • RRID:CVCL_AL89

https://web.expasy.org/cellosaurus/CVCL_AL89

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.

Proper citation: Coriell Cat# GM09762, RRID:CVCL_AL89 Copy   


  • RRID:CVCL_2Z77

https://web.expasy.org/cellosaurus/CVCL_2Z77

Organism: Homo sapiens (Human)
Disease: Nevoid basal cell carcinoma syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,ins(5;15)(5pter->5q23.2::15q23->15q26.1::5q23.2->5qter;15pter->15q23::15q26.1->15qter) (Coriell=GM09833)., Population: Caucasian; Irish.

Proper citation: RRID:CVCL_2Z77 Copy   


  • RRID:CVCL_AM09

https://web.expasy.org/cellosaurus/CVCL_AM09

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.

Proper citation: Coriell Cat# GM09784, RRID:CVCL_AM09 Copy   



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