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On page 87 showing 1721 ~ 1740 out of 95,747 results
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  • RRID:CVCL_0P92

https://web.expasy.org/cellosaurus/CVCL_0P92

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;21)(q11;p11) (PubMed=10377420)., Population: African American.

Proper citation: RRID:CVCL_0P92 Copy   


  • RRID:CVCL_F657

https://web.expasy.org/cellosaurus/CVCL_F657

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

Proper citation: Coriell Cat# GM01416, RRID:CVCL_F657 Copy   


  • RRID:CVCL_AV86

https://web.expasy.org/cellosaurus/CVCL_AV86

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

Proper citation: RRID:CVCL_AV86 Copy   


  • RRID:CVCL_J115

https://web.expasy.org/cellosaurus/CVCL_J115

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_J115 Copy   


  • RRID:CVCL_D872

https://web.expasy.org/cellosaurus/CVCL_D872

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

Proper citation: RRID:CVCL_D872 Copy   


  • RRID:CVCL_0M10

https://web.expasy.org/cellosaurus/CVCL_0M10

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

Proper citation: RRID:CVCL_0M10 Copy   


  • RRID:CVCL_X246

https://web.expasy.org/cellosaurus/CVCL_X246

Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,X,der(9)t(X;9)(q34;q12) (PubMed=10377420)., Population: African American.

Proper citation: Coriell Cat# GM01414, RRID:CVCL_X246 Copy   


  • RRID:CVCL_1Y25

https://web.expasy.org/cellosaurus/CVCL_1Y25

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

Proper citation: RRID:CVCL_1Y25 Copy   


  • RRID:CVCL_V830

https://web.expasy.org/cellosaurus/CVCL_V830

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(1;7)(1qter->1p34::7p13->7pter;7qter->7p13::1p34->1pter) (Coriell=GM01356)., Population: Caucasian.

Proper citation: RRID:CVCL_V830 Copy   


  • RRID:CVCL_2H13

https://web.expasy.org/cellosaurus/CVCL_2H13

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

Proper citation: RRID:CVCL_2H13 Copy   


  • RRID:CVCL_X251

https://web.expasy.org/cellosaurus/CVCL_X251

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

Proper citation: RRID:CVCL_X251 Copy   


  • RRID:CVCL_JD84

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JD84

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

Proper citation: Coriell Cat# GM01534, RRID:CVCL_JD84 Copy   


  • RRID:CVCL_M986

https://web.expasy.org/cellosaurus/CVCL_M986

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(5;12)(5pter->5q33::12q24->12qter;12pter->12q24::5q33->5qter) (Coriell=GM01536)., Population: African American., Part of: Human variation panel.

Proper citation: RRID:CVCL_M986 Copy   


  • RRID:CVCL_X250

https://web.expasy.org/cellosaurus/CVCL_X250

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

Proper citation: Coriell Cat# GM01535, RRID:CVCL_X250 Copy   


  • RRID:CVCL_2H22

https://web.expasy.org/cellosaurus/CVCL_2H22

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

Proper citation: Coriell Cat# GM01558, RRID:CVCL_2H22 Copy   


  • RRID:CVCL_EJ27

https://web.expasy.org/cellosaurus/CVCL_EJ27

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

Proper citation: RRID:CVCL_EJ27 Copy   


  • RRID:CVCL_AA15

https://web.expasy.org/cellosaurus/CVCL_AA15

Organism: Homo sapiens (Human)
Disease: Familial dysautonomia
Category: Transformed cell line
Comments:

Proper citation: Coriell Cat# GM01465, RRID:CVCL_AA15 Copy   


  • RRID:CVCL_V808

https://web.expasy.org/cellosaurus/CVCL_V808

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,t(4;11)(4pter->4q23::11q11->11qter;11pter->11q11::4q23->4qter) [8]; 45,X,t(4;11)(4pter->4q23::11q11->11qter;11pter->11q11::4q23->4qter),add(19)(?::p13.3->qter) [2] (Coriell=GM01561)., Population: Caucasian.

Proper citation: Coriell Cat# GM01561, RRID:CVCL_V808 Copy   


  • RRID:CVCL_4N14

https://web.expasy.org/cellosaurus/CVCL_4N14

Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type IIa
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_4N14 Copy   


  • RRID:CVCL_AI29

https://web.expasy.org/cellosaurus/CVCL_AI29

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

Proper citation: RRID:CVCL_AI29 Copy   



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