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On page 122 showing 2421 ~ 2440 out of 256,031 results
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  • RRID:CVCL_L486

https://web.expasy.org/cellosaurus/CVCL_L486

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

Proper citation: Coriell Cat# GM01362, RRID:CVCL_L486 Copy   


  • RRID:CVCL_1V13

https://web.expasy.org/cellosaurus/CVCL_1V13

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

Proper citation: RRID:CVCL_1V13 Copy   


  • RRID:CVCL_2H16

https://web.expasy.org/cellosaurus/CVCL_2H16

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

Proper citation: RRID:CVCL_2H16 Copy   


  • RRID:CVCL_V212

https://web.expasy.org/cellosaurus/CVCL_V212

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

Proper citation: RRID:CVCL_V212 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: Coriell Cat# GM01356, RRID:CVCL_V830 Copy   


  • RRID:CVCL_J114

https://web.expasy.org/cellosaurus/CVCL_J114

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,+der(9)(9pter->9q21.2::13q12.1->13qter)mat,-13 (Coriell=GM01387)., Population: Caucasian.

Proper citation: RRID:CVCL_J114 Copy   


  • RRID:CVCL_AE18

https://web.expasy.org/cellosaurus/CVCL_AE18

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

Proper citation: Coriell Cat# GM01453, RRID:CVCL_AE18 Copy   


  • RRID:CVCL_J113

https://web.expasy.org/cellosaurus/CVCL_J113

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

Proper citation: Coriell Cat# GM01388, RRID:CVCL_J113 Copy   


  • RRID:CVCL_9W81

https://web.expasy.org/cellosaurus/CVCL_9W81

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

Proper citation: RRID:CVCL_9W81 Copy   


  • RRID:CVCL_2H17

https://web.expasy.org/cellosaurus/CVCL_2H17

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

Proper citation: RRID:CVCL_2H17 Copy   


  • RRID:CVCL_V804

https://web.expasy.org/cellosaurus/CVCL_V804

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

Proper citation: RRID:CVCL_V804 Copy   


  • RRID:CVCL_1V14

https://web.expasy.org/cellosaurus/CVCL_1V14

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

Proper citation: Coriell Cat# GM01392, RRID:CVCL_1V14 Copy   


  • RRID:CVCL_7318

https://web.expasy.org/cellosaurus/CVCL_7318

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

Proper citation: RRID:CVCL_7318 Copy   


  • RRID:CVCL_L486

https://web.expasy.org/cellosaurus/CVCL_L486

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

Proper citation: RRID:CVCL_L486 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: 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_JD84

Possibly Discontinued

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

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

Proper citation: RRID:CVCL_JD84 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   



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