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On page 67 showing 1321 ~ 1340 out of 20,547 results
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  • RRID:CVCL_DA30

https://web.expasy.org/cellosaurus/CVCL_DA30

Organism: Homo sapiens (Human)
Disease: Neuronal ceroid lipofuscinosis type 2
Category: Finite cell line
Comments: Population: Asian.

Proper citation: Coriell Cat# GM09668, RRID:CVCL_DA30 Copy   


  • RRID:CVCL_AA86

https://web.expasy.org/cellosaurus/CVCL_AA86

Organism: Homo sapiens (Human)
Disease: Crigler-Najjar syndrome
Category: Finite cell line
Comments: Caution: Indicated as originating from a 1 year old female child in Coriell, but seems to contain both male and female cells (PubMed=33485181).

Proper citation: RRID:CVCL_AA86 Copy   


  • RRID:CVCL_FV56

https://web.expasy.org/cellosaurus/CVCL_FV56

Organism: Homo sapiens (Human)
Disease: Epidermolysis bullosa dystrophica
Category: Finite cell line
Comments: Population: African American.

Proper citation: Coriell Cat# GM09735, RRID:CVCL_FV56 Copy   


  • RRID:CVCL_9S94

https://web.expasy.org/cellosaurus/CVCL_9S94

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,rec(6)(pter->p12::q26->q16::p12->qter)pat (Coriell=GM09704).

Proper citation: RRID:CVCL_9S94 Copy   


  • RRID:CVCL_FV58

https://web.expasy.org/cellosaurus/CVCL_FV58

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

Proper citation: Coriell Cat# GM09739, RRID:CVCL_FV58 Copy   


  • RRID:CVCL_FV58

https://web.expasy.org/cellosaurus/CVCL_FV58

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

Proper citation: RRID:CVCL_FV58 Copy   


  • RRID:CVCL_X474

https://web.expasy.org/cellosaurus/CVCL_X474

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

Proper citation: RRID:CVCL_X474 Copy   


  • RRID:CVCL_2N13

https://web.expasy.org/cellosaurus/CVCL_2N13

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

Proper citation: RRID:CVCL_2N13 Copy   


  • RRID:CVCL_IN25

https://web.expasy.org/cellosaurus/CVCL_IN25

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

Proper citation: RRID:CVCL_IN25 Copy   


  • RRID:CVCL_2Z78

https://web.expasy.org/cellosaurus/CVCL_2Z78

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

Proper citation: Coriell Cat# GM09834, RRID:CVCL_2Z78 Copy   


  • RRID:CVCL_2N14

https://web.expasy.org/cellosaurus/CVCL_2N14

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,X,der(X)(Xpter->Xq21::Yq12->Yqter) (Coriell=GM09825).

Proper citation: Coriell Cat# GM09825, RRID:CVCL_2N14 Copy   


  • RRID:CVCL_2N14

https://web.expasy.org/cellosaurus/CVCL_2N14

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,X,der(X)(Xpter->Xq21::Yq12->Yqter) (Coriell=GM09825).

Proper citation: RRID:CVCL_2N14 Copy   


  • RRID:CVCL_2N13

https://web.expasy.org/cellosaurus/CVCL_2N13

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

Proper citation: Coriell Cat# GM09824, RRID:CVCL_2N13 Copy   


  • RRID:CVCL_7499

https://web.expasy.org/cellosaurus/CVCL_7499

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

Proper citation: RRID:CVCL_7499 Copy   


  • RRID:CVCL_6G95

https://web.expasy.org/cellosaurus/CVCL_6G95

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

Proper citation: RRID:CVCL_6G95 Copy   


  • RRID:CVCL_DS20

https://web.expasy.org/cellosaurus/CVCL_DS20

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

Proper citation: Coriell Cat# GM09885, RRID:CVCL_DS20 Copy   


  • RRID:CVCL_IN27

https://web.expasy.org/cellosaurus/CVCL_IN27

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

Proper citation: Coriell Cat# GM09894, RRID:CVCL_IN27 Copy   


  • RRID:CVCL_5P05

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_5P05

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

Proper citation: RRID:CVCL_5P05 Copy   


  • RRID:CVCL_5P05

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_5P05

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

Proper citation: Coriell Cat# GM09892, RRID:CVCL_5P05 Copy   


  • RRID:CVCL_IN26

https://web.expasy.org/cellosaurus/CVCL_IN26

Organism: Homo sapiens (Human)
Disease: Neonatal hemochromatosis
Category: Finite cell line
Comments: Population: Jewish.

Proper citation: Coriell Cat# GM09893, RRID:CVCL_IN26 Copy   



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