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On page 150 showing 2981 ~ 3000 out of 40,100 results
Snippet view Table view Download Top 1000 Results
Click the to add this resource to an Authentication Report or Collection
  • RRID:CVCL_X137

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

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

Proper citation: Coriell Cat# GM02820, RRID:CVCL_X137 Copy   


  • RRID:CVCL_X273

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

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

Proper citation: Coriell Cat# GM02836, RRID:CVCL_X273 Copy   


  • RRID:CVCL_CY25

https://web.expasy.org/cellosaurus/CVCL_CY25

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

Proper citation: Coriell Cat# GM02866, RRID:CVCL_CY25 Copy   


  • RRID:CVCL_L490

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

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

Proper citation: Coriell Cat# GM02852, RRID:CVCL_L490 Copy   


  • RRID:CVCL_1V25

https://web.expasy.org/cellosaurus/CVCL_1V25

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

Proper citation: Coriell Cat# GM02845, RRID:CVCL_1V25 Copy   


  • RRID:CVCL_7364

https://web.expasy.org/cellosaurus/CVCL_7364

Organism: Homo sapiens (Human)
Disease: Ataxia telangiectasia syndrome
Category: Transformed cell line
Comments: Population: Iranian.

Proper citation: Coriell Cat# GM02783, RRID:CVCL_7364 Copy   


  • RRID:CVCL_7363

https://web.expasy.org/cellosaurus/CVCL_7363

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Iranian., Part of: Human variation panel.

Proper citation: Coriell Cat# GM17335, RRID:CVCL_7363 Copy   


  • RRID:CVCL_7367

https://web.expasy.org/cellosaurus/CVCL_7367

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

Proper citation: Coriell Cat# GM02912, RRID:CVCL_7367 Copy   


  • RRID:CVCL_7369

https://web.expasy.org/cellosaurus/CVCL_7369

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

Proper citation: Coriell Cat# GM02937, RRID:CVCL_7369 Copy   


  • RRID:CVCL_9R75

https://web.expasy.org/cellosaurus/CVCL_9R75

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

Proper citation: Coriell Cat# GM02921, RRID:CVCL_9R75 Copy   


  • RRID:CVCL_X274

https://web.expasy.org/cellosaurus/CVCL_X274

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM02944, RRID:CVCL_X274 Copy   


  • RRID:CVCL_IN48

https://web.expasy.org/cellosaurus/CVCL_IN48

Organism: Homo sapiens (Human)
Disease: Neuropathy, hereditary sensory and autonomic, type IV
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM02958, RRID:CVCL_IN48 Copy   


  • RRID:CVCL_4Z93

https://web.expasy.org/cellosaurus/CVCL_4Z93

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

Proper citation: Coriell Cat# GM03010, RRID:CVCL_4Z93 Copy   


  • RRID:CVCL_AK25

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

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

Proper citation: Coriell Cat# GM02975, RRID:CVCL_AK25 Copy   


  • RRID:CVCL_X098

https://web.expasy.org/cellosaurus/CVCL_X098

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,inv(6)(pter->p23::q21->p23::q21->qter) (Coriell=GM02957)., Population: Caucasian.

Proper citation: Coriell Cat# GM02957, RRID:CVCL_X098 Copy   


  • RRID:CVCL_F128

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_F128

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

Proper citation: Coriell Cat# AG03022, RRID:CVCL_F128 Copy   


  • RRID:CVCL_L756

https://web.expasy.org/cellosaurus/CVCL_L756

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

Proper citation: Coriell Cat# GM02965, RRID:CVCL_L756 Copy   


  • RRID:CVCL_1N61

https://web.expasy.org/cellosaurus/CVCL_1N61

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(11;16)(11pter->11q13::16p11->16pter;16qter->16p11::11q13->11qter) (Coriell=GM03005)., Population: Caucasian.

Proper citation: Coriell Cat# GM03005, RRID:CVCL_1N61 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: Coriell Cat# GM02972, RRID:CVCL_DA22 Copy   


  • RRID:CVCL_GS17

https://web.expasy.org/cellosaurus/CVCL_GS17

Organism: Homo sapiens (Human)
Disease: Type 1 diabetes mellitus
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM02956, RRID:CVCL_GS17 Copy   



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