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On page 65 showing 1281 ~ 1300 out of 95,747 results
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  • RRID:CVCL_C416

https://web.expasy.org/cellosaurus/CVCL_C416

Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type IIa
Category: Induced pluripotent stem cell
Comments: Population: Iranian., From: Royan Institute; Theran; Iran.

Proper citation: RSCB Cat# RSCB0047, RRID:CVCL_C416 Copy   


  • RRID:CVCL_YY39

https://web.expasy.org/cellosaurus/CVCL_YY39

Organism: Homo sapiens (Human)
Category: Induced pluripotent stem cell
Comments: Population: Caucasian., Part of: Next Generation Genetic Association studies (Next Gen) program cell lines., Part of: Framingham Heart Study (FHS) collection.

Proper citation: RRID:CVCL_YY39 Copy   


  • RRID:CVCL_C417

https://web.expasy.org/cellosaurus/CVCL_C417

Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type IIa
Category: Induced pluripotent stem cell
Comments: Population: Iranian., From: Royan Institute; Theran; Iran.

Proper citation: RRID:CVCL_C417 Copy   


  • RRID:CVCL_A7RM

https://web.expasy.org/cellosaurus/CVCL_A7RM

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: 13th International Histocompatibility Workshop (13IHW) cell line panel.

Proper citation: RRID:CVCL_A7RM Copy   


  • RRID:CVCL_2N25

https://web.expasy.org/cellosaurus/CVCL_2N25

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

Proper citation: Coriell Cat# GM00403, RRID:CVCL_2N25 Copy   


  • RRID:CVCL_M921

https://web.expasy.org/cellosaurus/CVCL_M921

Organism: Homo sapiens (Human)
Disease: Sandhoff disease
Category: Finite cell line
Comments: Population: Mexican., Part of: Human variation panel.

Proper citation: RRID:CVCL_M921 Copy   


  • RRID:CVCL_F125

https://web.expasy.org/cellosaurus/CVCL_F125

Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group C
Category: Finite cell line
Comments: Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_F125 Copy   


  • RRID:CVCL_7288

https://web.expasy.org/cellosaurus/CVCL_7288

Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type IIa
Category: Finite cell line
Comments: Population: Caucasian; French Canadian.

Proper citation: RRID:CVCL_7288 Copy   


  • RRID:CVCL_H131

https://web.expasy.org/cellosaurus/CVCL_H131

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

Proper citation: RRID:CVCL_H131 Copy   


  • RRID:CVCL_V769

https://web.expasy.org/cellosaurus/CVCL_V769

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 45,XX,der(13;22)(13qter->13q10::22q10->22qter) (Coriell=GM00392)., Population: Caucasian.

Proper citation: RRID:CVCL_V769 Copy   


  • RRID:CVCL_J105

https://web.expasy.org/cellosaurus/CVCL_J105

Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Transformed cell line

Proper citation: RRID:CVCL_J105 Copy   


  • RRID:CVCL_2N25

https://web.expasy.org/cellosaurus/CVCL_2N25

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

Proper citation: RRID:CVCL_2N25 Copy   


  • RRID:CVCL_JD74

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JD74

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

Proper citation: Coriell Cat# GM00391, RRID:CVCL_JD74 Copy   


  • RRID:CVCL_V768

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_V768

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(4;11)(4pter->4q23::11q11->11qter;11pter->11q11::4q23->4qter) (Coriell=GM00380)., Population: Caucasian.

Proper citation: Coriell Cat# GM00380, RRID:CVCL_V768 Copy   


  • RRID:CVCL_V769

https://web.expasy.org/cellosaurus/CVCL_V769

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 45,XX,der(13;22)(13qter->13q10::22q10->22qter) (Coriell=GM00392)., Population: Caucasian.

Proper citation: Coriell Cat# GM00392, RRID:CVCL_V769 Copy   


  • RRID:CVCL_Y983

https://web.expasy.org/cellosaurus/CVCL_Y983

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

Proper citation: RRID:CVCL_Y983 Copy   


  • RRID:CVCL_J105

https://web.expasy.org/cellosaurus/CVCL_J105

Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Transformed cell line

Proper citation: Coriell Cat# GM00467, RRID:CVCL_J105 Copy   


  • RRID:CVCL_M921

https://web.expasy.org/cellosaurus/CVCL_M921

Organism: Homo sapiens (Human)
Disease: Sandhoff disease
Category: Finite cell line
Comments: Population: Mexican., Part of: Human variation panel.

Proper citation: Coriell Cat# GM00470, RRID:CVCL_M921 Copy   


  • RRID:CVCL_4N04

https://web.expasy.org/cellosaurus/CVCL_4N04

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

Proper citation: RRID:CVCL_4N04 Copy   


  • RRID:CVCL_1Y19

https://web.expasy.org/cellosaurus/CVCL_1Y19

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

Proper citation: RRID:CVCL_1Y19 Copy   



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