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On page 114 showing 2261 ~ 2280 out of 19,458 results
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  • RRID:CVCL_1A88

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_1A88

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines.

Proper citation: RRID:CVCL_1A88 Copy   


  • RRID:CVCL_F637

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_F637

Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type II
Category: Transformed cell line
Comments: Population: African American.

Proper citation: RRID:CVCL_F637 Copy   


  • RRID:CVCL_1B05

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_1B05

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines.

Proper citation: Coriell Cat# GM20312, RRID:CVCL_1B05 Copy   


  • RRID:CVCL_1A96

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_1A96

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines.

Proper citation: Coriell Cat# GM20285, RRID:CVCL_1A96 Copy   


  • RRID:CVCL_7660

Discontinued

https://web.expasy.org/cellosaurus/CVCL_7660

Organism: Homo sapiens (Human)
Disease: Roberts-SC phocomelia syndrome
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_7660 Copy   


  • RRID:CVCL_1B26

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_1B26

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines.

Proper citation: Coriell Cat# GM20413, RRID:CVCL_1B26 Copy   


  • RRID:CVCL_5S34

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_5S34

Organism: Homo sapiens (Human)
Disease: 1p36 deletion syndrome
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_5S34 Copy   


  • RRID:CVCL_F184

Possibly Discontinued

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

Organism: Homo sapiens (Human)
Disease:
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)
Disease:
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)
Disease:
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)
Disease:
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
Comments:

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
Comments:

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
Comments:

Proper citation: RRID:CVCL_4T59 Copy   


  • RRID:CVCL_0Q31

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_0Q31

Organism: Homo sapiens (Human)
Disease: Nijmegen breakage syndrome
Category: Finite cell line
Comments: Population: Caucasian; Czechoslovakian.

Proper citation: RRID:CVCL_0Q31 Copy   


  • RRID:CVCL_1S97

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_1S97

Organism: Cricetulus griseus (Chinese hamster)
Disease:
Category: Hybrid cell line
Comments: Group: Human/rodent somatic cell hybrid.

Proper citation: Coriell Cat# GM15776, RRID:CVCL_1S97 Copy   


  • RRID:CVCL_5Q62

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_5Q62

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

Proper citation: RRID:CVCL_5Q62 Copy   


  • RRID:CVCL_A5WN

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_A5WN

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

Proper citation: RRID:CVCL_A5WN Copy   


  • RRID:CVCL_A5WI

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_A5WI

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

Proper citation: RRID:CVCL_A5WI Copy   


  • RRID:CVCL_A5WF

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_A5WF

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

Proper citation: RRID:CVCL_A5WF Copy   



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