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On page 277 showing 5521 ~ 5540 out of 95,747 results
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  • RRID:CVCL_4D34

https://web.expasy.org/cellosaurus/CVCL_4D34

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

Proper citation: Coriell Cat# GM16968, RRID:CVCL_4D34 Copy   


  • RRID:CVCL_4F75

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_4F75

Organism: Homo sapiens (Human)
Disease: Peroxisome biogenesis disorder 7A
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_4F75 Copy   


  • RRID:CVCL_AB22

https://web.expasy.org/cellosaurus/CVCL_AB22

Organism: Homo sapiens (Human)
Disease: Familial dysautonomia
Category: Transformed cell line
Comments: Donor information: Established from monozygotic twin of GM16771 (Cellosaurus=CVCL_AB21)., Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_AB22 Copy   


  • RRID:CVCL_4D32

https://web.expasy.org/cellosaurus/CVCL_4D32

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

Proper citation: RRID:CVCL_4D32 Copy   


  • RRID:CVCL_1F67

https://web.expasy.org/cellosaurus/CVCL_1F67

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

Proper citation: RRID:CVCL_1F67 Copy   


  • RRID:CVCL_CZ71

https://web.expasy.org/cellosaurus/CVCL_CZ71

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

Proper citation: Coriell Cat# GM16787, RRID:CVCL_CZ71 Copy   


  • RRID:CVCL_4D31

https://web.expasy.org/cellosaurus/CVCL_4D31

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

Proper citation: RRID:CVCL_4D31 Copy   


  • RRID:CVCL_1F68

https://web.expasy.org/cellosaurus/CVCL_1F68

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

Proper citation: Coriell Cat# GM16800, RRID:CVCL_1F68 Copy   


  • RRID:CVCL_9Z52

https://web.expasy.org/cellosaurus/CVCL_9Z52

Organism: Homo sapiens (Human)
Disease: Peroxisome biogenesis disorder 7B
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_9Z52 Copy   


  • RRID:CVCL_AK43

https://web.expasy.org/cellosaurus/CVCL_AK43

Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group C
Category: Finite cell line

Proper citation: Coriell Cat# GM16754, RRID:CVCL_AK43 Copy   


  • RRID:CVCL_1F67

https://web.expasy.org/cellosaurus/CVCL_1F67

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

Proper citation: Coriell Cat# GM16799, RRID:CVCL_1F67 Copy   


  • RRID:CVCL_4D32

https://web.expasy.org/cellosaurus/CVCL_4D32

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

Proper citation: Coriell Cat# GM16966, RRID:CVCL_4D32 Copy   


  • RRID:CVCL_5Q79

https://web.expasy.org/cellosaurus/CVCL_5Q79

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

Proper citation: RRID:CVCL_5Q79 Copy   


  • RRID:CVCL_N268

https://web.expasy.org/cellosaurus/CVCL_N268

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

Proper citation: Coriell Cat# GM18098, RRID:CVCL_N268 Copy   


  • RRID:CVCL_AB18

https://web.expasy.org/cellosaurus/CVCL_AB18

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_AB18 Copy   


  • RRID:CVCL_U754

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_U754

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

Proper citation: RRID:CVCL_U754 Copy   


  • RRID:CVCL_5Q81

https://web.expasy.org/cellosaurus/CVCL_5Q81

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

Proper citation: Coriell Cat# GM16810, RRID:CVCL_5Q81 Copy   


  • RRID:CVCL_4D33

https://web.expasy.org/cellosaurus/CVCL_4D33

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

Proper citation: Coriell Cat# GM16967, RRID:CVCL_4D33 Copy   


  • RRID:CVCL_AB21

https://web.expasy.org/cellosaurus/CVCL_AB21

Organism: Homo sapiens (Human)
Disease: Familial dysautonomia
Category: Transformed cell line
Comments: Donor information: Established from monozygotic twin of GM16772 (Cellosaurus=CVCL_AB22)., Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_AB21 Copy   


  • RRID:CVCL_4D26

https://web.expasy.org/cellosaurus/CVCL_4D26

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

Proper citation: RRID:CVCL_4D26 Copy   



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