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On page 103 showing 2041 ~ 2060 out of 236,573 results
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  • RRID:CVCL_X247

https://web.expasy.org/cellosaurus/CVCL_X247

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;9)(q13;q34) (PubMed=10377420)., Population: African American.

Proper citation: Coriell Cat# GM01429, RRID:CVCL_X247 Copy   


  • RRID:CVCL_X247

https://web.expasy.org/cellosaurus/CVCL_X247

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;9)(q13;q34) (PubMed=10377420)., Population: African American.

Proper citation: RRID:CVCL_X247 Copy   


  • RRID:CVCL_F028

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_F028

Organism: Homo sapiens (Human)
Disease: Xeroderma pigmentosum, complementation group E
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_F028 Copy   


  • RRID:CVCL_4N09

https://web.expasy.org/cellosaurus/CVCL_4N09

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

Proper citation: Coriell Cat# GM01355, RRID:CVCL_4N09 Copy   


  • RRID:CVCL_4N16

https://web.expasy.org/cellosaurus/CVCL_4N16

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

Proper citation: RRID:CVCL_4N16 Copy   


  • RRID:CVCL_2H18

https://web.expasy.org/cellosaurus/CVCL_2H18

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

Proper citation: RRID:CVCL_2H18 Copy   


  • RRID:CVCL_AI27

https://web.expasy.org/cellosaurus/CVCL_AI27

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_AI27 Copy   


  • RRID:CVCL_7320

https://web.expasy.org/cellosaurus/CVCL_7320

Organism: Homo sapiens (Human)
Disease: Bloom syndrome
Category: Finite cell line
Comments: Donor information: From Bloom Syndrome Registry patient 44(AbRu) (BSR44)., Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_7320 Copy   


  • RRID:CVCL_1F07

https://web.expasy.org/cellosaurus/CVCL_1F07

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

Proper citation: RRID:CVCL_1F07 Copy   


  • RRID:CVCL_T813

https://web.expasy.org/cellosaurus/CVCL_T813

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

Proper citation: RRID:CVCL_T813 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: Coriell Cat# GM17153, RRID:CVCL_M986 Copy   


  • RRID:CVCL_4N15

https://web.expasy.org/cellosaurus/CVCL_4N15

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

Proper citation: Coriell Cat# GM01459, RRID:CVCL_4N15 Copy   


  • RRID:CVCL_9Y81

https://web.expasy.org/cellosaurus/CVCL_9Y81

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

Proper citation: Coriell Cat# GM01501, RRID:CVCL_9Y81 Copy   


  • RRID:CVCL_V807

https://web.expasy.org/cellosaurus/CVCL_V807

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

Proper citation: Coriell Cat# GM01555, RRID:CVCL_V807 Copy   


  • RRID:CVCL_X081

https://web.expasy.org/cellosaurus/CVCL_X081

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

Proper citation: RRID:CVCL_X081 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: Coriell Cat# GM01536, RRID:CVCL_M986 Copy   


  • RRID:CVCL_IZ38

https://web.expasy.org/cellosaurus/CVCL_IZ38

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

Proper citation: Coriell Cat# GM01455, RRID:CVCL_IZ38 Copy   


  • RRID:CVCL_H973

https://web.expasy.org/cellosaurus/CVCL_H973

Organism: Homo sapiens (Human)
Disease: Maturity-onset diabetes of the young
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_H973 Copy   


  • RRID:CVCL_2H19

https://web.expasy.org/cellosaurus/CVCL_2H19

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

Proper citation: RRID:CVCL_2H19 Copy   


  • RRID:CVCL_4N15

https://web.expasy.org/cellosaurus/CVCL_4N15

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

Proper citation: RRID:CVCL_4N15 Copy   



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