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On page 481 showing 9601 ~ 9620 out of 95,747 results
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  • RRID:CVCL_5S75

https://web.expasy.org/cellosaurus/CVCL_5S75

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

Proper citation: RRID:CVCL_5S75 Copy   


  • RRID:CVCL_5S86

https://web.expasy.org/cellosaurus/CVCL_5S86

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

Proper citation: Coriell Cat# GM23270, RRID:CVCL_5S86 Copy   


  • RRID:CVCL_U546

https://web.expasy.org/cellosaurus/CVCL_U546

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

Proper citation: RRID:CVCL_U546 Copy   


  • RRID:CVCL_BV45

https://web.expasy.org/cellosaurus/CVCL_BV45

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

Proper citation: RRID:CVCL_BV45 Copy   


  • RRID:CVCL_AZ45

https://web.expasy.org/cellosaurus/CVCL_AZ45

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

Proper citation: RRID:CVCL_AZ45 Copy   


  • RRID:CVCL_BV45

https://web.expasy.org/cellosaurus/CVCL_BV45

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

Proper citation: Coriell Cat# GM23349, RRID:CVCL_BV45 Copy   


  • RRID:CVCL_EG03

https://web.expasy.org/cellosaurus/CVCL_EG03

Organism: Homo sapiens (Human)
Disease: 2-hydroxyglutaric aciduria
Category: Transformed cell line

Proper citation: Coriell Cat# GM23295, RRID:CVCL_EG03 Copy   


  • RRID:CVCL_BV33

https://web.expasy.org/cellosaurus/CVCL_BV33

Organism: Homo sapiens (Human)
Disease: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
Category: Transformed cell line

Proper citation: RRID:CVCL_BV33 Copy   


  • RRID:CVCL_EG03

https://web.expasy.org/cellosaurus/CVCL_EG03

Organism: Homo sapiens (Human)
Disease: 2-hydroxyglutaric aciduria
Category: Transformed cell line

Proper citation: RRID:CVCL_EG03 Copy   


  • RRID:CVCL_BV47

https://web.expasy.org/cellosaurus/CVCL_BV47

Organism: Homo sapiens (Human)
Disease: Dystrophia myotonica 2
Category: Transformed cell line

Proper citation: Coriell Cat# GM23355, RRID:CVCL_BV47 Copy   


  • RRID:CVCL_BV49

https://web.expasy.org/cellosaurus/CVCL_BV49

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

Proper citation: RRID:CVCL_BV49 Copy   


  • RRID:CVCL_BV52

https://web.expasy.org/cellosaurus/CVCL_BV52

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

Proper citation: Coriell Cat# GM23367, RRID:CVCL_BV52 Copy   


  • RRID:CVCL_BV44

https://web.expasy.org/cellosaurus/CVCL_BV44

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

Proper citation: RRID:CVCL_BV44 Copy   


  • RRID:CVCL_JF24

https://web.expasy.org/cellosaurus/CVCL_JF24

Organism: Homo sapiens (Human)
Disease: Muscular dystrophy-dystroglycanopathy (limb-girdle) type C, 1
Category: Finite cell line

Proper citation: RRID:CVCL_JF24 Copy   


  • RRID:CVCL_BX01

https://web.expasy.org/cellosaurus/CVCL_BX01

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

Proper citation: Coriell Cat# GM23321, RRID:CVCL_BX01 Copy   


  • RRID:CVCL_AZ45

https://web.expasy.org/cellosaurus/CVCL_AZ45

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

Proper citation: Coriell Cat# GM23301, RRID:CVCL_AZ45 Copy   


  • RRID:CVCL_4T43

https://web.expasy.org/cellosaurus/CVCL_4T43

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

Proper citation: RRID:CVCL_4T43 Copy   


  • RRID:CVCL_4T43

https://web.expasy.org/cellosaurus/CVCL_4T43

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

Proper citation: Coriell Cat# GM23305, RRID:CVCL_4T43 Copy   


  • RRID:CVCL_F196

https://web.expasy.org/cellosaurus/CVCL_F196

Organism: Homo sapiens (Human)
Disease: Merosin-deficient congenital muscular dystrophy type 1A
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_F196 Copy   


  • RRID:CVCL_BV48

https://web.expasy.org/cellosaurus/CVCL_BV48

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

Proper citation: Coriell Cat# GM23357, RRID:CVCL_BV48 Copy   



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