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On page 168 showing 3341 ~ 3360 out of 20,547 results
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  • RRID:CVCL_0M13

https://web.expasy.org/cellosaurus/CVCL_0M13

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

Proper citation: RRID:CVCL_0M13 Copy   


  • RRID:CVCL_W661

https://web.expasy.org/cellosaurus/CVCL_W661

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

Proper citation: RRID:CVCL_W661 Copy   


  • RRID:CVCL_F020

https://web.expasy.org/cellosaurus/CVCL_F020

Organism: Homo sapiens (Human)
Disease: Hepatocyte nuclear factor 4-alpha associated monogenic diabetes
Category: Finite cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.

Proper citation: RRID:CVCL_F020 Copy   


  • RRID:CVCL_JB89

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JB89

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

Proper citation: Coriell Cat# GM02006, RRID:CVCL_JB89 Copy   


  • RRID:CVCL_M989

https://web.expasy.org/cellosaurus/CVCL_M989

Organism: Homo sapiens (Human)
Disease: Ataxia with isolated vitamin E deficiency
Category: Finite cell line
Comments: Population: Mexican., Part of: Human variation panel.

Proper citation: RRID:CVCL_M989 Copy   


  • RRID:CVCL_4E25

https://web.expasy.org/cellosaurus/CVCL_4E25

Organism: Homo sapiens (Human)
Disease: Sea-blue histiocyte syndrome
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM01912, RRID:CVCL_4E25 Copy   


  • RRID:CVCL_JD67

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JD67

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

Proper citation: RRID:CVCL_JD67 Copy   


  • RRID:CVCL_X259

https://web.expasy.org/cellosaurus/CVCL_X259

Organism: Homo sapiens (Human)
Disease: Trisomy 8
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_X259 Copy   


  • RRID:CVCL_V466

https://web.expasy.org/cellosaurus/CVCL_V466

Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XX,i(21)(qter->q10::q10->qter) [13]; 46,XX [87] (Coriell=GM02058)., Population: Jewish; Ashkenazi.

Proper citation: Coriell Cat# GM02058, RRID:CVCL_V466 Copy   


  • RRID:CVCL_1H43

https://web.expasy.org/cellosaurus/CVCL_1H43

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments: Donor information: At sampling donor was not affected with Huntington disease but at 25% risk for disease., Population: Caucasian.

Proper citation: Coriell Cat# GM02123, RRID:CVCL_1H43 Copy   


  • RRID:CVCL_CW69

https://web.expasy.org/cellosaurus/CVCL_CW69

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

Proper citation: RRID:CVCL_CW69 Copy   


  • RRID:CVCL_U703

https://web.expasy.org/cellosaurus/CVCL_U703

Organism: Homo sapiens (Human)
Disease: Bloom syndrome
Category: Finite cell line
Comments: Donor information: From Bloom Syndrome Registry patient 53(StAs) (BSR53)., Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_U703 Copy   


  • RRID:CVCL_1H41

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_1H41

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

Proper citation: RRID:CVCL_1H41 Copy   


  • RRID:CVCL_M990

https://web.expasy.org/cellosaurus/CVCL_M990

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Arab., Part of: Human variation panel.

Proper citation: RRID:CVCL_M990 Copy   


  • RRID:CVCL_H177

https://web.expasy.org/cellosaurus/CVCL_H177

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

Proper citation: RRID:CVCL_H177 Copy   


  • RRID:CVCL_W640

https://web.expasy.org/cellosaurus/CVCL_W640

Organism: Homo sapiens (Human)
Disease: I-cell disease
Category: Finite cell line
Comments: Population: Arab.

Proper citation: RRID:CVCL_W640 Copy   


  • RRID:CVCL_CW70

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_CW70

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

Proper citation: RRID:CVCL_CW70 Copy   


  • RRID:CVCL_V825

https://web.expasy.org/cellosaurus/CVCL_V825

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

Proper citation: RRID:CVCL_V825 Copy   


  • RRID:CVCL_W621

https://web.expasy.org/cellosaurus/CVCL_W621

Organism: Homo sapiens (Human)
Disease: Wolman disease
Category: Finite cell line
Comments: Population: African American.

Proper citation: RRID:CVCL_W621 Copy   


  • RRID:CVCL_2Z72

https://web.expasy.org/cellosaurus/CVCL_2Z72

Organism: Homo sapiens (Human)
Disease: Nevoid basal cell carcinoma syndrome
Category: Finite cell line
Comments: Characteristics: Hypersensitive to cell killing by ionizing radiation (Coriell=GM02098)., Population: Caucasian.

Proper citation: RRID:CVCL_2Z72 Copy   



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