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On page 408 showing 8141 ~ 8160 out of 236,573 results
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  • RRID:CVCL_L490

https://web.expasy.org/cellosaurus/CVCL_L490

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

Proper citation: RRID:CVCL_L490 Copy   


  • RRID:CVCL_CY26

https://web.expasy.org/cellosaurus/CVCL_CY26

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

Proper citation: RRID:CVCL_CY26 Copy   


  • RRID:CVCL_FA32

https://web.expasy.org/cellosaurus/CVCL_FA32

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

Proper citation: Coriell Cat# GM02814, RRID:CVCL_FA32 Copy   


  • RRID:CVCL_1V26

https://web.expasy.org/cellosaurus/CVCL_1V26

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

Proper citation: Coriell Cat# GM02846, RRID:CVCL_1V26 Copy   


  • RRID:CVCL_M930

https://web.expasy.org/cellosaurus/CVCL_M930

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(9;12)(9qter->9p13::12q24->12qter;12pter->12q24::9p13->9pter) (Coriell=GM02821)., Population: African American.

Proper citation: Coriell Cat# GM02821, RRID:CVCL_M930 Copy   


  • RRID:CVCL_4N32

https://web.expasy.org/cellosaurus/CVCL_4N32

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

Proper citation: RRID:CVCL_4N32 Copy   


  • RRID:CVCL_9W91

https://web.expasy.org/cellosaurus/CVCL_9W91

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

Proper citation: RRID:CVCL_9W91 Copy   


  • RRID:CVCL_9R73

https://web.expasy.org/cellosaurus/CVCL_9R73

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

Proper citation: RRID:CVCL_9R73 Copy   


  • RRID:CVCL_4Z90

https://web.expasy.org/cellosaurus/CVCL_4Z90

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

Proper citation: Coriell Cat# GM02830, RRID:CVCL_4Z90 Copy   


  • RRID:CVCL_0Q52

https://web.expasy.org/cellosaurus/CVCL_0Q52

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

Proper citation: RRID:CVCL_0Q52 Copy   


  • RRID:CVCL_L470

https://web.expasy.org/cellosaurus/CVCL_L470

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

Proper citation: RRID:CVCL_L470 Copy   


  • RRID:CVCL_M932

https://web.expasy.org/cellosaurus/CVCL_M932

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;11)(q11.1;p13) (PubMed=10377420)., Population: South American (Brazil, Guyana, Venezuela)., Part of: Human variation panel.

Proper citation: RRID:CVCL_M932 Copy   


  • RRID:CVCL_X137

https://web.expasy.org/cellosaurus/CVCL_X137

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

Proper citation: RRID:CVCL_X137 Copy   


  • RRID:CVCL_1N31

https://web.expasy.org/cellosaurus/CVCL_1N31

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(3;16)(3pter->3q13.2::16q13->16qter;16pter->16q13::3q13.2->3qter) (Coriell=GM02860)., Population: Caucasian.

Proper citation: Coriell Cat# GM02860, RRID:CVCL_1N31 Copy   


  • RRID:CVCL_X273

https://web.expasy.org/cellosaurus/CVCL_X273

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

Proper citation: RRID:CVCL_X273 Copy   


  • RRID:CVCL_CW71

https://web.expasy.org/cellosaurus/CVCL_CW71

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

Proper citation: Coriell Cat# GM02870, RRID:CVCL_CW71 Copy   


  • RRID:CVCL_4D82

https://web.expasy.org/cellosaurus/CVCL_4D82

Organism: Homo sapiens (Human)
Disease: Ring chromosome 14 syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XY,r(14) (Coriell=GM03003)., Population: Caucasian.

Proper citation: Coriell Cat# GM03003, RRID:CVCL_4D82 Copy   


  • RRID:CVCL_7370

https://web.expasy.org/cellosaurus/CVCL_7370

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XY [43]; 46,XY,t(7;9)(7pter->7q36::9q12->9qter;9pter->9q12::7q36->qter) [7] (Coriell=GM02987)., Population: Caucasian.

Proper citation: Coriell Cat# GM02987, RRID:CVCL_7370 Copy   


  • RRID:CVCL_AX19

https://web.expasy.org/cellosaurus/CVCL_AX19

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

Proper citation: RRID:CVCL_AX19 Copy   


  • RRID:CVCL_X099

https://web.expasy.org/cellosaurus/CVCL_X099

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XY,del(18)(pter>q21) (Coriell=GM02980)., Population: Caucasian.

Proper citation: Coriell Cat# GM02980, RRID:CVCL_X099 Copy   



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