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On page 483 showing 9641 ~ 9660 out of 95,747 results
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  • RRID:CVCL_F194

https://web.expasy.org/cellosaurus/CVCL_F194

Organism: Homo sapiens (Human)
Category: Induced pluripotent stem cell
Comments: Population: African American.

Proper citation: Coriell Cat# GM23413, RRID:CVCL_F194 Copy   


  • RRID:CVCL_JF43

https://web.expasy.org/cellosaurus/CVCL_JF43

Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth disease
Category: Transformed cell line

Proper citation: RRID:CVCL_JF43 Copy   


  • RRID:CVCL_Y711

https://web.expasy.org/cellosaurus/CVCL_Y711

Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line

Proper citation: RRID:CVCL_Y711 Copy   


  • RRID:CVCL_T817

https://web.expasy.org/cellosaurus/CVCL_T817

Organism: Homo sapiens (Human)
Category: Induced pluripotent stem cell
Comments: Population: African American.

Proper citation: Coriell Cat# GM23446, RRID:CVCL_T817 Copy   


  • RRID:CVCL_BV71

https://web.expasy.org/cellosaurus/CVCL_BV71

Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth disease
Category: Transformed cell line

Proper citation: Coriell Cat# GM23445, RRID:CVCL_BV71 Copy   


  • RRID:CVCL_BX02

https://web.expasy.org/cellosaurus/CVCL_BX02

Organism: Homo sapiens (Human)
Disease: Emery-Dreifuss muscular dystrophy 2, autosomal dominant
Category: Transformed cell line

Proper citation: RRID:CVCL_BX02 Copy   


  • RRID:CVCL_F192

https://web.expasy.org/cellosaurus/CVCL_F192

Organism: Homo sapiens (Human)
Disease: Friedreich ataxia
Category: Induced pluripotent stem cell
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_F192 Copy   


  • RRID:CVCL_V034

https://web.expasy.org/cellosaurus/CVCL_V034

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

Proper citation: RRID:CVCL_V034 Copy   


  • RRID:CVCL_Y716

https://web.expasy.org/cellosaurus/CVCL_Y716

Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Comments: Donor information: At sampling donor was asymptomatic for ornithine carbamoyltransferase deficiency.

Proper citation: RRID:CVCL_Y716 Copy   


  • RRID:CVCL_T841

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_T841

Organism: Homo sapiens (Human)
Category: Induced pluripotent stem cell
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM23476, RRID:CVCL_T841 Copy   


  • RRID:CVCL_Y712

https://web.expasy.org/cellosaurus/CVCL_Y712

Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Comments: Donor information: At sampling donor was asymptomatic for ornithine carbamoyltransferase deficiency.

Proper citation: RRID:CVCL_Y712 Copy   


  • RRID:CVCL_GS98

https://web.expasy.org/cellosaurus/CVCL_GS98

Organism: Homo sapiens (Human)
Disease: Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Category: Transformed cell line

Proper citation: RRID:CVCL_GS98 Copy   


  • RRID:CVCL_BV73

https://web.expasy.org/cellosaurus/CVCL_BV73

Organism: Homo sapiens (Human)
Disease: Rett syndrome
Category: Transformed cell line
Comments: Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_BV73 Copy   


  • RRID:CVCL_JF43

https://web.expasy.org/cellosaurus/CVCL_JF43

Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth disease
Category: Transformed cell line

Proper citation: Coriell Cat# GM23424, RRID:CVCL_JF43 Copy   


  • RRID:CVCL_U549

https://web.expasy.org/cellosaurus/CVCL_U549

Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line

Proper citation: Coriell Cat# GM23466, RRID:CVCL_U549 Copy   


  • RRID:CVCL_5M30

https://web.expasy.org/cellosaurus/CVCL_5M30

Organism: Homo sapiens (Human)
Disease: Citrullinemia type I
Category: Transformed cell line

Proper citation: RRID:CVCL_5M30 Copy   


  • RRID:CVCL_U549

https://web.expasy.org/cellosaurus/CVCL_U549

Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line

Proper citation: RRID:CVCL_U549 Copy   


  • RRID:CVCL_GS98

https://web.expasy.org/cellosaurus/CVCL_GS98

Organism: Homo sapiens (Human)
Disease: Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Category: Transformed cell line

Proper citation: Coriell Cat# GM23420, RRID:CVCL_GS98 Copy   


  • RRID:CVCL_F168

https://web.expasy.org/cellosaurus/CVCL_F168

Organism: Homo sapiens (Human)
Disease: Dystrophia myotonica 1
Category: Transformed cell line
Comments: Population: Caucasian; English/German.

Proper citation: RRID:CVCL_F168 Copy   


  • RRID:CVCL_Y717

https://web.expasy.org/cellosaurus/CVCL_Y717

Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line

Proper citation: RRID:CVCL_Y717 Copy   



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