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On page 103 showing 2041 ~ 2060 out of 20,547 results
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  • RRID:CVCL_5M81

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_5M81

Organism: Homo sapiens (Human)
Disease: Sporadic retinoblastoma
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;13)(p22jq12) (PubMed=10377420)., Population: Caucasian.

Proper citation: Coriell Cat# GM02971, RRID:CVCL_5M81 Copy   


  • RRID:CVCL_AX00

https://web.expasy.org/cellosaurus/CVCL_AX00

Organism: Homo sapiens (Human)
Disease: Leri-Weill dyschondrosteosis
Category: Finite cell line
Comments: Population: Caucasian; French.

Proper citation: Coriell Cat# GM02885, RRID:CVCL_AX00 Copy   


  • RRID:CVCL_DA22

https://web.expasy.org/cellosaurus/CVCL_DA22

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

Proper citation: RRID:CVCL_DA22 Copy   


  • RRID:CVCL_X099

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

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

Proper citation: RRID:CVCL_X099 Copy   


  • RRID:CVCL_DD73

https://web.expasy.org/cellosaurus/CVCL_DD73

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

Proper citation: Coriell Cat# GM02962, RRID:CVCL_DD73 Copy   


  • RRID:CVCL_AX21

https://web.expasy.org/cellosaurus/CVCL_AX21

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

Proper citation: RRID:CVCL_AX21 Copy   


  • RRID:CVCL_U507

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_U507

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

Proper citation: RRID:CVCL_U507 Copy   


  • RRID:CVCL_GT47

https://web.expasy.org/cellosaurus/CVCL_GT47

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

Proper citation: RRID:CVCL_GT47 Copy   


  • RRID:CVCL_H962

https://web.expasy.org/cellosaurus/CVCL_H962

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;3)(Xpter->Xq28::3q21->3qter;3pter->3q21::Xq28->Xqter) (Coriell=GM02899)., Population: Caucasian; Finnish.

Proper citation: Coriell Cat# GM02899, RRID:CVCL_H962 Copy   


  • RRID:CVCL_GT47

https://web.expasy.org/cellosaurus/CVCL_GT47

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

Proper citation: Coriell Cat# GM03015, RRID:CVCL_GT47 Copy   


  • RRID:CVCL_JX70

https://web.expasy.org/cellosaurus/CVCL_JX70

Organism: Homo sapiens (Human)
Disease: 5 alpha steroid reductase 2 deficiency
Category: Finite cell line
Comments: Population: Arab.

Proper citation: Coriell Cat# GM02935, RRID:CVCL_JX70 Copy   


  • RRID:CVCL_X097

https://web.expasy.org/cellosaurus/CVCL_X097

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,rec(1)dup(q)ins(1)(pter->p22::q32->q31::p22->qter)pat (Coriell=GM02946)., Population: Caucasian.

Proper citation: Coriell Cat# GM02946, RRID:CVCL_X097 Copy   


  • RRID:CVCL_V818

https://web.expasy.org/cellosaurus/CVCL_V818

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Senescence: Senesces at 24 PDL (PubMed=6492896)., Population: Caucasian.

Proper citation: Coriell Cat# GM02881, RRID:CVCL_V818 Copy   


  • RRID:CVCL_9R76

https://web.expasy.org/cellosaurus/CVCL_9R76

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

Proper citation: Coriell Cat# GM02922, RRID:CVCL_9R76 Copy   


  • RRID:CVCL_5M81

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_5M81

Organism: Homo sapiens (Human)
Disease: Sporadic retinoblastoma
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;13)(p22jq12) (PubMed=10377420)., Population: Caucasian.

Proper citation: Coriell Cat# AG02971, RRID:CVCL_5M81 Copy   


  • RRID:CVCL_AK25

https://web.expasy.org/cellosaurus/CVCL_AK25

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

Proper citation: RRID:CVCL_AK25 Copy   


  • RRID:CVCL_7370

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

Organism: Homo sapiens (Human)
Disease:
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: RRID:CVCL_7370 Copy   


  • RRID:CVCL_X276

https://web.expasy.org/cellosaurus/CVCL_X276

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,rec(3)(qter->p25::q21->qter)pat (Coriell=GM03039)., Population: Caucasian.

Proper citation: Coriell Cat# GM03039, RRID:CVCL_X276 Copy   


  • RRID:CVCL_X278

https://web.expasy.org/cellosaurus/CVCL_X278

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,rec(3)(qter->p25::q21->qter)pat (Coriell=GM03085)., Population: Caucasian; French Canadian.

Proper citation: RRID:CVCL_X278 Copy   


  • RRID:CVCL_7374

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7374

Organism: Homo sapiens (Human)
Disease: Niemann-Pick disease, type C1
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_7374 Copy   



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