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On page 251 showing 5001 ~ 5020 out of 256,031 results
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  • RRID:CVCL_CX27

Discontinued

https://web.expasy.org/cellosaurus/CVCL_CX27

Organism: Homo sapiens (Human)
Disease: I-cell disease
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_CX27 Copy   


  • RRID:CVCL_X082

https://web.expasy.org/cellosaurus/CVCL_X082

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,del(9)(qter>p22) (Coriell=GM01667)., Population: Caucasian.

Proper citation: Coriell Cat# GM01667, RRID:CVCL_X082 Copy   


  • RRID:CVCL_2Z69

https://web.expasy.org/cellosaurus/CVCL_2Z69

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

Proper citation: RRID:CVCL_2Z69 Copy   


  • RRID:CVCL_0D84

https://web.expasy.org/cellosaurus/CVCL_0D84

Organism: Homo sapiens (Human)
Disease: Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_0D84 Copy   


  • RRID:CVCL_X082

https://web.expasy.org/cellosaurus/CVCL_X082

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,del(9)(qter>p22) (Coriell=GM01667)., Population: Caucasian.

Proper citation: RRID:CVCL_X082 Copy   


  • RRID:CVCL_0M02

https://web.expasy.org/cellosaurus/CVCL_0M02

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

Proper citation: RRID:CVCL_0M02 Copy   


  • RRID:CVCL_7334

Discontinued

https://web.expasy.org/cellosaurus/CVCL_7334

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

Proper citation: Coriell Cat# GM00237, RRID:CVCL_7334 Copy   


  • RRID:CVCL_V810

https://web.expasy.org/cellosaurus/CVCL_V810

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,der(17)(17qter->17p13::13q14->13qter)mat (Coriell=GM01663)., Population: Caucasian.

Proper citation: RRID:CVCL_V810 Copy   


  • RRID:CVCL_U518

https://web.expasy.org/cellosaurus/CVCL_U518

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

Proper citation: RRID:CVCL_U518 Copy   


  • RRID:CVCL_JC92

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JC92

Organism: Homo sapiens (Human)
Disease: Ataxia telangiectasia syndrome
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_JC92 Copy   


  • RRID:CVCL_X254

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_X254

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

Proper citation: Coriell Cat# GM01724, RRID:CVCL_X254 Copy   


  • RRID:CVCL_2Z71

https://web.expasy.org/cellosaurus/CVCL_2Z71

Organism: Homo sapiens (Human)
Disease: Nevoid basal cell carcinoma syndrome
Category: Transformed cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM01726, RRID:CVCL_2Z71 Copy   


  • RRID:CVCL_1R61

https://web.expasy.org/cellosaurus/CVCL_1R61

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,der(21)(21qter->21p11::Xq11->Xqter)mat (Coriell=GM01730)., Population: African American.

Proper citation: Coriell Cat# GM01730, RRID:CVCL_1R61 Copy   


  • RRID:CVCL_1F09

https://web.expasy.org/cellosaurus/CVCL_1F09

Organism: Homo sapiens (Human)
Disease: Xeroderma pigmentosum, complementation group C
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_1F09 Copy   


  • RRID:CVCL_X083

https://web.expasy.org/cellosaurus/CVCL_X083

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,del(18)(qter>p11) (Coriell=GM01727)., Population: Caucasian.

Proper citation: RRID:CVCL_X083 Copy   


  • RRID:CVCL_AM86

https://web.expasy.org/cellosaurus/CVCL_AM86

Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type II
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM01691, RRID:CVCL_AM86 Copy   


  • RRID:CVCL_JC91

https://web.expasy.org/cellosaurus/CVCL_JC91

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

Proper citation: Coriell Cat# GM01721, RRID:CVCL_JC91 Copy   


  • RRID:CVCL_AD63

https://web.expasy.org/cellosaurus/CVCL_AD63

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

Proper citation: RRID:CVCL_AD63 Copy   


  • RRID:CVCL_F602

https://web.expasy.org/cellosaurus/CVCL_F602

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

Proper citation: RRID:CVCL_F602 Copy   


  • RRID:CVCL_U518

https://web.expasy.org/cellosaurus/CVCL_U518

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

Proper citation: Coriell Cat# GM01685, RRID:CVCL_U518 Copy   



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