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On page 392 showing 7821 ~ 7840 out of 19,458 results
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  • RRID:CVCL_0H58

Possibly Discontinued

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

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

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)
Disease:
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)
Disease:
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)
Disease:
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
Comments:

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)
Disease:
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
Comments:

Proper citation: RRID:CVCL_F206 Copy   


  • RRID:CVCL_4D72

Possibly Discontinued

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

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

Proper citation: RRID:CVCL_4D72 Copy   


  • RRID:CVCL_DA57

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_DA57

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

Proper citation: RRID:CVCL_DA57 Copy   


  • RRID:CVCL_3718

Discontinued

https://web.expasy.org/cellosaurus/CVCL_3718

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Senescence: Capable of at least ~30 PDL (ATCC=CRL-2607)., Part of: Wistar Institute Special Collection vascular cell lines.

Proper citation: RRID:CVCL_3718 Copy   


  • RRID:CVCL_8224

Misidentified

https://web.expasy.org/cellosaurus/CVCL_8224

Organism: Sus scrofa (Pig)
Disease:
Category: Undefined cell line type
Comments: Problematic cell line: Misidentified. Originally thought to be of human origin and originate from a 27 year old female patient with papillary carcinoma but found to be from pig (PubMed=10508494; PubMed=20143388)..

Proper citation: RRID:CVCL_8224 Copy   


  • RRID:CVCL_3A55

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_3A55

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

Proper citation: Coriell Cat# HQ00056, RRID:CVCL_3A55 Copy   


  • RRID:CVCL_3A54

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_3A54

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

Proper citation: RRID:CVCL_3A54 Copy   


  • RRID:CVCL_2Y33

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_2Y33

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

Proper citation: RRID:CVCL_2Y33 Copy   


  • RRID:CVCL_AE98

Discontinued

https://web.expasy.org/cellosaurus/CVCL_AE98

Organism: Homo sapiens (Human)
Disease:
Category: Induced pluripotent stem cell
Comments: From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom., From: Cambridge BioResource; Cambridge; United Kingdom.

Proper citation: EBiSC Cat# WTSIi054-B, RRID:CVCL_AE98 Copy   


  • RRID:CVCL_AE98

Discontinued

https://web.expasy.org/cellosaurus/CVCL_AE98

Organism: Homo sapiens (Human)
Disease:
Category: Induced pluripotent stem cell
Comments: From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom., From: Cambridge BioResource; Cambridge; United Kingdom.

Proper citation: RRID:CVCL_AE98 Copy   


  • RRID:CVCL_E687

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_E687

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel.

Proper citation: ECACC Cat# 94082249, RRID:CVCL_E687 Copy   


  • RRID:CVCL_0F62

    This resource has 1+ mentions.

Misidentified Discontinued Discontinued

https://web.expasy.org/cellosaurus/CVCL_0F62

Organism: Mus musculus (Mouse)
Disease:
Category: Undefined cell line type
Comments: Problematic cell line: Misidentified. Originally thought to be a microgial cell of rat origin (3 day old Wistar rat) but found to be from mouse (Millipore)..

Proper citation: RRID:CVCL_0F62 Copy   


  • RRID:CVCL_0F62

    This resource has 1+ mentions.

Misidentified Discontinued Discontinued

https://web.expasy.org/cellosaurus/CVCL_0F62

Organism: Mus musculus (Mouse)
Disease:
Category: Undefined cell line type
Comments: Problematic cell line: Misidentified. Originally thought to be a microgial cell of rat origin (3 day old Wistar rat) but found to be from mouse (Millipore)..

Proper citation: Millipore Cat# SCC103, RRID:CVCL_0F62 Copy   



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