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On page 95 showing 1881 ~ 1900 out of 20,547 results
Snippet view Table view Download Top 1000 Results
Click the to add this resource to an Authentication Report or Collection
  • RRID:CVCL_IL12

https://web.expasy.org/cellosaurus/CVCL_IL12

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

Proper citation: RRID:CVCL_IL12 Copy   


  • RRID:CVCL_9R72

https://web.expasy.org/cellosaurus/CVCL_9R72

Organism: Homo sapiens (Human)
Disease: Neuraminidase deficiency
Category: Finite cell line
Comments:

Proper citation: Coriell Cat# GM02685, RRID:CVCL_9R72 Copy   


  • RRID:CVCL_DD72

https://web.expasy.org/cellosaurus/CVCL_DD72

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

Proper citation: RRID:CVCL_DD72 Copy   


  • RRID:CVCL_2N08

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_2N08

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

Proper citation: RRID:CVCL_2N08 Copy   


  • RRID:CVCL_IL13

https://web.expasy.org/cellosaurus/CVCL_IL13

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY (Coriell=GM02715)., Population: Caucasian.

Proper citation: RRID:CVCL_IL13 Copy   


  • RRID:CVCL_M928

https://web.expasy.org/cellosaurus/CVCL_M928

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

Proper citation: RRID:CVCL_M928 Copy   


  • RRID:CVCL_5M80

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_5M80

Organism: Homo sapiens (Human)
Disease: Sporadic retinoblastoma
Category: Finite cell line
Comments:

Proper citation: Coriell Cat# AG02718, RRID:CVCL_5M80 Copy   


  • RRID:CVCL_X270

https://web.expasy.org/cellosaurus/CVCL_X270

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 47,XY,+der(15)(15pter->15q13::15p11->15pter) (Coriell=GM02729)., Population: Caucasian.

Proper citation: Coriell Cat# GM02729, RRID:CVCL_X270 Copy   


  • RRID:CVCL_CY15

https://web.expasy.org/cellosaurus/CVCL_CY15

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

Proper citation: RRID:CVCL_CY15 Copy   


  • RRID:CVCL_5M80

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_5M80

Organism: Homo sapiens (Human)
Disease: Sporadic retinoblastoma
Category: Finite cell line
Comments:

Proper citation: Coriell Cat# GM02718, RRID:CVCL_5M80 Copy   


  • RRID:CVCL_AM84

https://web.expasy.org/cellosaurus/CVCL_AM84

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

Proper citation: Coriell Cat# GM02691, RRID:CVCL_AM84 Copy   


  • RRID:CVCL_CY17

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_CY17

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

Proper citation: Coriell Cat# GM02710, RRID:CVCL_CY17 Copy   


  • RRID:CVCL_1L44

https://web.expasy.org/cellosaurus/CVCL_1L44

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

Proper citation: RRID:CVCL_1L44 Copy   


  • RRID:CVCL_L489

https://web.expasy.org/cellosaurus/CVCL_L489

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

Proper citation: RRID:CVCL_L489 Copy   


  • RRID:CVCL_L470

https://web.expasy.org/cellosaurus/CVCL_L470

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

Proper citation: Coriell Cat# GM02838, RRID:CVCL_L470 Copy   


  • RRID:CVCL_4N30

https://web.expasy.org/cellosaurus/CVCL_4N30

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

Proper citation: Coriell Cat# GM02768, RRID:CVCL_4N30 Copy   


  • RRID:CVCL_X272

https://web.expasy.org/cellosaurus/CVCL_X272

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,+13,der(13;15)(13qter->q10::q10->15qter)mat (Coriell=GM02813)., Population: Caucasian.

Proper citation: Coriell Cat# GM02813, RRID:CVCL_X272 Copy   


  • RRID:CVCL_X095

https://web.expasy.org/cellosaurus/CVCL_X095

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,del(5)(qter->p14) (Coriell=GM02800)., Population: African American.

Proper citation: Coriell Cat# GM02800, RRID:CVCL_X095 Copy   


  • RRID:CVCL_0M15

https://web.expasy.org/cellosaurus/CVCL_0M15

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

Proper citation: RRID:CVCL_0M15 Copy   


  • RRID:CVCL_0M19

https://web.expasy.org/cellosaurus/CVCL_0M19

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

Proper citation: RRID:CVCL_0M19 Copy   



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