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On page 94 showing 1861 ~ 1880 out of 95,747 results
Snippet view Table view Download Top 1000 Results
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  • RRID:CVCL_L949

https://web.expasy.org/cellosaurus/CVCL_L949

Organism: Homo sapiens (Human)
Disease: Familial adenomatous polyposis
Category: Transformed cell line
Comments: Population: Caucasian; British.

Proper citation: RRID:CVCL_L949 Copy   


  • RRID:CVCL_F094

https://web.expasy.org/cellosaurus/CVCL_F094

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: African American., Part of: Human variation panel.

Proper citation: RRID:CVCL_F094 Copy   


  • RRID:CVCL_N005

https://web.expasy.org/cellosaurus/CVCL_N005

Organism: Homo sapiens (Human)
Disease: Supernumerary circular chromosome
Category: Finite cell line
Comments: Population: Caucasian; Greek., Part of: Human variation panel.

Proper citation: Coriell Cat# GM17373, RRID:CVCL_N005 Copy   


  • RRID:CVCL_9W94

https://web.expasy.org/cellosaurus/CVCL_9W94

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

Proper citation: RRID:CVCL_9W94 Copy   


  • RRID:CVCL_Y091

https://web.expasy.org/cellosaurus/CVCL_Y091

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;11)(q22;q13) (PubMed=10377420)., Population: Caucasian.

Proper citation: Coriell Cat# GM03322, RRID:CVCL_Y091 Copy   


  • RRID:CVCL_N005

https://web.expasy.org/cellosaurus/CVCL_N005

Organism: Homo sapiens (Human)
Disease: Supernumerary circular chromosome
Category: Finite cell line
Comments: Population: Caucasian; Greek., Part of: Human variation panel.

Proper citation: RRID:CVCL_N005 Copy   


  • RRID:CVCL_2Z76

https://web.expasy.org/cellosaurus/CVCL_2Z76

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

Proper citation: Coriell Cat# GM03300, RRID:CVCL_2Z76 Copy   


  • RRID:CVCL_F093

https://web.expasy.org/cellosaurus/CVCL_F093

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

Proper citation: RRID:CVCL_F093 Copy   


  • RRID:CVCL_F093

https://web.expasy.org/cellosaurus/CVCL_F093

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

Proper citation: Coriell Cat# GM03325, RRID:CVCL_F093 Copy   


  • RRID:CVCL_4Z85

https://web.expasy.org/cellosaurus/CVCL_4Z85

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

Proper citation: RRID:CVCL_4Z85 Copy   


  • RRID:CVCL_H191

https://web.expasy.org/cellosaurus/CVCL_H191

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

Proper citation: Coriell Cat# GM03336, RRID:CVCL_H191 Copy   


  • RRID:CVCL_2S87

https://web.expasy.org/cellosaurus/CVCL_2S87

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

Proper citation: RRID:CVCL_2S87 Copy   


  • RRID:CVCL_N005

https://web.expasy.org/cellosaurus/CVCL_N005

Organism: Homo sapiens (Human)
Disease: Supernumerary circular chromosome
Category: Finite cell line
Comments: Population: Caucasian; Greek., Part of: Human variation panel.

Proper citation: Coriell Cat# GM03321, RRID:CVCL_N005 Copy   


  • RRID:CVCL_1L48

https://web.expasy.org/cellosaurus/CVCL_1L48

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

Proper citation: RRID:CVCL_1L48 Copy   


  • RRID:CVCL_2S91

https://web.expasy.org/cellosaurus/CVCL_2S91

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(6;12)(6pter->6q21::12p13->12pter;12qter->12p13::6q21->6qter) (Coriell=GM03404).

Proper citation: Coriell Cat# GM03404, RRID:CVCL_2S91 Copy   


  • RRID:CVCL_2S90

https://web.expasy.org/cellosaurus/CVCL_2S90

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(11;22)(11pter->11q23::22q11->22qter;22pter->22q11::11q23->11qter) (Coriell=GM03372)., Population: African American.

Proper citation: Coriell Cat# GM03372, RRID:CVCL_2S90 Copy   


  • RRID:CVCL_2S92

https://web.expasy.org/cellosaurus/CVCL_2S92

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(9;14)(9qter->9p22::14q13->14qter;14pter->14q13::9p22->9pter) (Coriell=GM03463)., Population: Caucasian.

Proper citation: Coriell Cat# GM03463, RRID:CVCL_2S92 Copy   


  • RRID:CVCL_DA25

https://web.expasy.org/cellosaurus/CVCL_DA25

Organism: Homo sapiens (Human)
Disease: Niemann-Pick disease, type B
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM03393, RRID:CVCL_DA25 Copy   


  • RRID:CVCL_1L45

https://web.expasy.org/cellosaurus/CVCL_1L45

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

Proper citation: RRID:CVCL_1L45 Copy   


  • RRID:CVCL_H148

https://web.expasy.org/cellosaurus/CVCL_H148

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

Proper citation: Coriell Cat# GM03400, RRID:CVCL_H148 Copy   



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