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On page 240 showing 4781 ~ 4800 out of 256,031 results
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  • RRID:CVCL_DD79

https://web.expasy.org/cellosaurus/CVCL_DD79

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

Proper citation: RRID:CVCL_DD79 Copy   


  • RRID:CVCL_5N28

https://web.expasy.org/cellosaurus/CVCL_5N28

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

Proper citation: Coriell Cat# GM05172, RRID:CVCL_5N28 Copy   


  • RRID:CVCL_5N07

https://web.expasy.org/cellosaurus/CVCL_5N07

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

Proper citation: RRID:CVCL_5N07 Copy   


  • RRID:CVCL_AA53

https://web.expasy.org/cellosaurus/CVCL_AA53

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

Proper citation: RRID:CVCL_AA53 Copy   


  • RRID:CVCL_F291

https://web.expasy.org/cellosaurus/CVCL_F291

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

Proper citation: Coriell Cat# GM05160, RRID:CVCL_F291 Copy   


  • RRID:CVCL_5N22

https://web.expasy.org/cellosaurus/CVCL_5N22

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

Proper citation: RRID:CVCL_5N22 Copy   


  • RRID:CVCL_1K22

https://web.expasy.org/cellosaurus/CVCL_1K22

Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth disease type 1A
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_1K22 Copy   


  • RRID:CVCL_AA57

https://web.expasy.org/cellosaurus/CVCL_AA57

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

Proper citation: RRID:CVCL_AA57 Copy   


  • RRID:CVCL_X319

https://web.expasy.org/cellosaurus/CVCL_X319

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,del(1)(pter->q41::q43->qter) (Coriell=GM05302)., Population: Caucasian.

Proper citation: RRID:CVCL_X319 Copy   


  • RRID:CVCL_GQ42

https://web.expasy.org/cellosaurus/CVCL_GQ42

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

Proper citation: Coriell Cat# GM05217, RRID:CVCL_GQ42 Copy   


  • RRID:CVCL_0P51

https://web.expasy.org/cellosaurus/CVCL_0P51

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

Proper citation: RRID:CVCL_0P51 Copy   


  • RRID:CVCL_AW66

https://web.expasy.org/cellosaurus/CVCL_AW66

Organism: Homo sapiens (Human)
Disease: Dystrophia myotonica 1
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_AW66 Copy   


  • RRID:CVCL_GQ45

https://web.expasy.org/cellosaurus/CVCL_GQ45

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

Proper citation: Coriell Cat# GM05220, RRID:CVCL_GQ45 Copy   


  • RRID:CVCL_GQ50

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_GQ50

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

Proper citation: RRID:CVCL_GQ50 Copy   


  • RRID:CVCL_GQ53

https://web.expasy.org/cellosaurus/CVCL_GQ53

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

Proper citation: Coriell Cat# GM05236, RRID:CVCL_GQ53 Copy   


  • RRID:CVCL_X320

https://web.expasy.org/cellosaurus/CVCL_X320

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

Proper citation: Coriell Cat# GM05319, RRID:CVCL_X320 Copy   


  • RRID:CVCL_2T11

https://web.expasy.org/cellosaurus/CVCL_2T11

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

Proper citation: RRID:CVCL_2T11 Copy   


  • RRID:CVCL_GQ46

https://web.expasy.org/cellosaurus/CVCL_GQ46

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

Proper citation: RRID:CVCL_GQ46 Copy   


  • RRID:CVCL_GY27

https://web.expasy.org/cellosaurus/CVCL_GY27

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

Proper citation: Coriell Cat# GM05301, RRID:CVCL_GY27 Copy   


  • RRID:CVCL_GQ55

https://web.expasy.org/cellosaurus/CVCL_GQ55

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

Proper citation: Coriell Cat# GM05240, RRID:CVCL_GQ55 Copy   



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