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On page 210 showing 4181 ~ 4200 out of 95,747 results
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  • RRID:CVCL_GQ63

https://web.expasy.org/cellosaurus/CVCL_GQ63

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

Proper citation: Coriell Cat# GM06128, RRID:CVCL_GQ63 Copy   


  • RRID:CVCL_7448

https://web.expasy.org/cellosaurus/CVCL_7448

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

Proper citation: RRID:CVCL_7448 Copy   


  • RRID:CVCL_5U20

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_5U20

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

Proper citation: Coriell Cat# GM06097, RRID:CVCL_5U20 Copy   


  • RRID:CVCL_GQ64

https://web.expasy.org/cellosaurus/CVCL_GQ64

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

Proper citation: Coriell Cat# GM06139, RRID:CVCL_GQ64 Copy   


  • RRID:CVCL_1N87

https://web.expasy.org/cellosaurus/CVCL_1N87

Organism: Homo sapiens (Human)
Disease: Tuberous sclerosis 2
Category: Transformed cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_1N87 Copy   


  • RRID:CVCL_CV42

https://web.expasy.org/cellosaurus/CVCL_CV42

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,rec(9)(pter->q22.1::q34.3->q34.1::q22.1->qter)mat (Coriell=GM06074)., Population: Caucasian.

Proper citation: RRID:CVCL_CV42 Copy   


  • RRID:CVCL_CZ17

https://web.expasy.org/cellosaurus/CVCL_CZ17

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

Proper citation: RRID:CVCL_CZ17 Copy   


  • RRID:CVCL_CZ85

https://web.expasy.org/cellosaurus/CVCL_CZ85

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

Proper citation: Coriell Cat# GM06091, RRID:CVCL_CZ85 Copy   


  • RRID:CVCL_GZ41

https://web.expasy.org/cellosaurus/CVCL_GZ41

Organism: Homo sapiens (Human)
Disease: Schinzel-Giedion midface-retraction syndrome
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_GZ41 Copy   


  • RRID:CVCL_F669

https://web.expasy.org/cellosaurus/CVCL_F669

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

Proper citation: Coriell Cat# GM06229, RRID:CVCL_F669 Copy   


  • RRID:CVCL_5N41

https://web.expasy.org/cellosaurus/CVCL_5N41

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

Proper citation: Coriell Cat# GM06230, RRID:CVCL_5N41 Copy   


  • RRID:CVCL_1J33

https://web.expasy.org/cellosaurus/CVCL_1J33

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

Proper citation: RRID:CVCL_1J33 Copy   


  • RRID:CVCL_9X01

https://web.expasy.org/cellosaurus/CVCL_9X01

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

Proper citation: RRID:CVCL_9X01 Copy   


  • RRID:CVCL_N051

https://web.expasy.org/cellosaurus/CVCL_N051

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

Proper citation: RRID:CVCL_N051 Copy   


  • RRID:CVCL_F670

https://web.expasy.org/cellosaurus/CVCL_F670

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

Proper citation: Coriell Cat# GM06275, RRID:CVCL_F670 Copy   


  • RRID:CVCL_W048

https://web.expasy.org/cellosaurus/CVCL_W048

Organism: Homo sapiens (Human)
Disease: Trichothiodystrophy 4, nonphotosensitive
Category: Finite cell line
Comments: Population: Moroccan.

Proper citation: RRID:CVCL_W048 Copy   


  • RRID:CVCL_CY54

https://web.expasy.org/cellosaurus/CVCL_CY54

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

Proper citation: RRID:CVCL_CY54 Copy   


  • RRID:CVCL_V046

https://web.expasy.org/cellosaurus/CVCL_V046

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

Proper citation: Coriell Cat# GM06274, RRID:CVCL_V046 Copy   


  • RRID:CVCL_2T20

https://web.expasy.org/cellosaurus/CVCL_2T20

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

Proper citation: Coriell Cat# GM06228, RRID:CVCL_2T20 Copy   


  • RRID:CVCL_N050

https://web.expasy.org/cellosaurus/CVCL_N050

Organism: Homo sapiens (Human)
Disease: Peroxisome biogenesis disorder 8A
Category: Finite cell line
Comments: Population: Africans north of the Sahara., Part of: Human variation panel.

Proper citation: RRID:CVCL_N050 Copy   



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