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On page 105 showing 2081 ~ 2100 out of 20,547 results
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  • RRID:CVCL_AX80

https://web.expasy.org/cellosaurus/CVCL_AX80

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

Proper citation: RRID:CVCL_AX80 Copy   


  • RRID:CVCL_DD78

https://web.expasy.org/cellosaurus/CVCL_DD78

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

Proper citation: Coriell Cat# GM05181, RRID:CVCL_DD78 Copy   


  • RRID:CVCL_DS13

https://web.expasy.org/cellosaurus/CVCL_DS13

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

Proper citation: RRID:CVCL_DS13 Copy   


  • RRID:CVCL_X317

https://web.expasy.org/cellosaurus/CVCL_X317

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,der(14)(14qter->14p11.2::20p11.1->20pter)mat (Coriell=GM05133)., Population: African American.

Proper citation: Coriell Cat# GM05133, RRID:CVCL_X317 Copy   


  • RRID:CVCL_1K28

https://web.expasy.org/cellosaurus/CVCL_1K28

Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth disease type 1A
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM05167, RRID:CVCL_1K28 Copy   


  • RRID:CVCL_AW62

https://web.expasy.org/cellosaurus/CVCL_AW62

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

Proper citation: Coriell Cat# GM05208, RRID:CVCL_AW62 Copy   


  • RRID:CVCL_1K28

https://web.expasy.org/cellosaurus/CVCL_1K28

Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth disease type 1A
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_1K28 Copy   


  • RRID:CVCL_1Q24

https://web.expasy.org/cellosaurus/CVCL_1Q24

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(6;7)(q21;q21.2) (Coriell=GM05183)., Population: Caucasian; Italian.

Proper citation: RRID:CVCL_1Q24 Copy   


  • RRID:CVCL_5N18

https://web.expasy.org/cellosaurus/CVCL_5N18

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

Proper citation: RRID:CVCL_5N18 Copy   


  • RRID:CVCL_5N14

https://web.expasy.org/cellosaurus/CVCL_5N14

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

Proper citation: RRID:CVCL_5N14 Copy   


  • RRID:CVCL_AX78

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_AX78

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

Proper citation: RRID:CVCL_AX78 Copy   


  • RRID:CVCL_AX78

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_AX78

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

Proper citation: Coriell Cat# GM05131, RRID:CVCL_AX78 Copy   


  • RRID:CVCL_AW58

https://web.expasy.org/cellosaurus/CVCL_AW58

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

Proper citation: RRID:CVCL_AW58 Copy   


  • RRID:CVCL_AX79

https://web.expasy.org/cellosaurus/CVCL_AX79

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

Proper citation: Coriell Cat# GM05132, RRID:CVCL_AX79 Copy   


  • RRID:CVCL_5N05

https://web.expasy.org/cellosaurus/CVCL_5N05

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

Proper citation: Coriell Cat# GM05087, RRID:CVCL_5N05 Copy   


  • RRID:CVCL_5N26

https://web.expasy.org/cellosaurus/CVCL_5N26

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

Proper citation: RRID:CVCL_5N26 Copy   


  • RRID:CVCL_1K26

https://web.expasy.org/cellosaurus/CVCL_1K26

Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth disease type 1A
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_1K26 Copy   


  • RRID:CVCL_2T10

https://web.expasy.org/cellosaurus/CVCL_2T10

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

Proper citation: Coriell Cat# GM05235, RRID:CVCL_2T10 Copy   


  • RRID:CVCL_0P48

https://web.expasy.org/cellosaurus/CVCL_0P48

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

Proper citation: RRID:CVCL_0P48 Copy   


  • RRID:CVCL_9W99

https://web.expasy.org/cellosaurus/CVCL_9W99

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

Proper citation: RRID:CVCL_9W99 Copy   



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