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On page 245 showing 4881 ~ 4900 out of 19,458 results
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  • RRID:CVCL_F184

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_F184

Organism: Homo sapiens (Human)
Category: Induced pluripotent stem cell
Comments: Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection.

Proper citation: RRID:CVCL_F184 Copy   


  • RRID:CVCL_F179

    This resource has 1+ mentions.

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_F179

Organism: Homo sapiens (Human)
Category: Induced pluripotent stem cell
Comments: Caution: May be identical to one of the many iPSC cell lines produced from HDF1388 by the Center for iPS Cell Research and Application (CiRA)., Population: Caucasian.

Proper citation: Coriell Cat# GM23280, RRID:CVCL_F179 Copy   


  • RRID:CVCL_F166

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_F166

Organism: Homo sapiens (Human)
Category: Induced pluripotent stem cell
Comments: Population: African American.

Proper citation: RRID:CVCL_F166 Copy   


  • RRID:CVCL_F166

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_F166

Organism: Homo sapiens (Human)
Category: Induced pluripotent stem cell
Comments: Population: African American.

Proper citation: Coriell Cat# GM23394, RRID:CVCL_F166 Copy   


  • RRID:CVCL_4T52

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_4T52

Organism: Homo sapiens (Human)
Disease: Ullrich congenital muscular dystrophy
Category: Finite cell line

Proper citation: RRID:CVCL_4T52 Copy   


  • RRID:CVCL_5T33

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_5T33

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

Proper citation: RRID:CVCL_5T33 Copy   


  • RRID:CVCL_4T59

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_4T59

Organism: Homo sapiens (Human)
Disease: Ullrich congenital muscular dystrophy
Category: Finite cell line

Proper citation: RRID:CVCL_4T59 Copy   


  • RRID:CVCL_1N90

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_1N90

Organism: Homo sapiens (Human)
Category: Induced pluripotent stem cell
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM24581, RRID:CVCL_1N90 Copy   


  • RRID:CVCL_A5WM

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_A5WM

Organism: Homo sapiens (Human)
Disease: Facioscapulohumeral muscular dystrophy 1
Category: Transformed cell line

Proper citation: RRID:CVCL_A5WM Copy   


  • RRID:CVCL_A5WR

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_A5WR

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

Proper citation: Coriell Cat# GM16330, RRID:CVCL_A5WR Copy   


  • RRID:CVCL_0H58

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_0H58

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

Proper citation: RRID:CVCL_0H58 Copy   


  • RRID:CVCL_0H57

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_0H57

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

Proper citation: Coriell Cat# GM16434, RRID:CVCL_0H57 Copy   


  • RRID:CVCL_0H58

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_0H58

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

Proper citation: Coriell Cat# GM16436, RRID:CVCL_0H58 Copy   


  • RRID:CVCL_YP91

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_YP91

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

Proper citation: RRID:CVCL_YP91 Copy   


  • RRID:CVCL_YP91

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_YP91

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

Proper citation: Coriell Cat# GM16733, RRID:CVCL_YP91 Copy   


  • RRID:CVCL_YP92

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_YP92

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

Proper citation: Coriell Cat# GM16735, RRID:CVCL_YP92 Copy   


  • RRID:CVCL_9Z53

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_9Z53

Organism: Homo sapiens (Human)
Disease: Peroxisome biogenesis disorder 7B
Category: Finite cell line

Proper citation: RRID:CVCL_9Z53 Copy   


  • RRID:CVCL_H530

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_H530

Organism: Homo sapiens (Human)
Disease: Facioscapulohumeral muscular dystrophy 1
Category: Finite cell line
Comments: Senescence: Capable of at least 32 PDL (Coriell=GM17731).

Proper citation: RRID:CVCL_H530 Copy   


  • RRID:CVCL_4D72

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_4D72

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

Proper citation: Coriell Cat# GM17957, RRID:CVCL_4D72 Copy   


  • RRID:CVCL_F206

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_F206

Organism: Homo sapiens (Human)
Disease: Facioscapulohumeral muscular dystrophy 1
Category: Finite cell line

Proper citation: RRID:CVCL_F206 Copy   



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