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On page 389 showing 7761 ~ 7780 out of 256,031 results
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  • RRID:CVCL_8A85

https://web.expasy.org/cellosaurus/CVCL_8A85

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

Proper citation: Coriell Cat# GM06812, RRID:CVCL_8A85 Copy   


  • RRID:CVCL_Y703

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_Y703

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

Proper citation: RRID:CVCL_Y703 Copy   


  • RRID:CVCL_UR72

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_UR72

Organism: Homo sapiens (Human)
Disease: Isovaleric acidemia
Category: Finite cell line
Comments:

Proper citation: Coriell Cat# GM06836, RRID:CVCL_UR72 Copy   


  • RRID:CVCL_5N47

https://web.expasy.org/cellosaurus/CVCL_5N47

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

Proper citation: RRID:CVCL_5N47 Copy   


  • RRID:CVCL_2Z58

https://web.expasy.org/cellosaurus/CVCL_2Z58

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

Proper citation: RRID:CVCL_2Z58 Copy   


  • RRID:CVCL_7459

https://web.expasy.org/cellosaurus/CVCL_7459

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel.

Proper citation: RRID:CVCL_7459 Copy   


  • RRID:CVCL_7459

https://web.expasy.org/cellosaurus/CVCL_7459

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel.

Proper citation: Coriell Cat# GM06862, RRID:CVCL_7459 Copy   


  • RRID:CVCL_F297

https://web.expasy.org/cellosaurus/CVCL_F297

Organism: Homo sapiens (Human)
Disease: Familial adenomatous polyposis
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_F297 Copy   


  • RRID:CVCL_FA33

https://web.expasy.org/cellosaurus/CVCL_FA33

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

Proper citation: RRID:CVCL_FA33 Copy   


  • RRID:CVCL_GQ67

https://web.expasy.org/cellosaurus/CVCL_GQ67

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

Proper citation: Coriell Cat# GM06876, RRID:CVCL_GQ67 Copy   


  • RRID:CVCL_N056

https://web.expasy.org/cellosaurus/CVCL_N056

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: African American., Part of: Human variation panel.

Proper citation: Coriell Cat# GM17104, RRID:CVCL_N056 Copy   


  • RRID:CVCL_AX97

https://web.expasy.org/cellosaurus/CVCL_AX97

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

Proper citation: RRID:CVCL_AX97 Copy   


  • RRID:CVCL_AD70

https://web.expasy.org/cellosaurus/CVCL_AD70

Organism: Homo sapiens (Human)
Disease: X-linked centronuclear myopathy
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_AD70 Copy   


  • RRID:CVCL_AX93

https://web.expasy.org/cellosaurus/CVCL_AX93

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

Proper citation: RRID:CVCL_AX93 Copy   


  • RRID:CVCL_5N51

https://web.expasy.org/cellosaurus/CVCL_5N51

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,del(10)(p13->qter) (Coriell=GM06937)., Population: Caucasian.

Proper citation: RRID:CVCL_5N51 Copy   


  • RRID:CVCL_F594

https://web.expasy.org/cellosaurus/CVCL_F594

Organism: Homo sapiens (Human)
Disease: Fanconi anemia
Category: Transformed cell line
Comments: Population: Arab.

Proper citation: RRID:CVCL_F594 Copy   


  • RRID:CVCL_GQ67

https://web.expasy.org/cellosaurus/CVCL_GQ67

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

Proper citation: RRID:CVCL_GQ67 Copy   


  • RRID:CVCL_5N48

https://web.expasy.org/cellosaurus/CVCL_5N48

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+i(18)(pter->p10::p10->pter) (Coriell=GM06871).

Proper citation: RRID:CVCL_5N48 Copy   


  • RRID:CVCL_F609

https://web.expasy.org/cellosaurus/CVCL_F609

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

Proper citation: RRID:CVCL_F609 Copy   


  • RRID:CVCL_AX86

https://web.expasy.org/cellosaurus/CVCL_AX86

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

Proper citation: RRID:CVCL_AX86 Copy   



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