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On page 54 showing 1061 ~ 1080 out of 95,747 results
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  • RRID:CVCL_HQ51

https://web.expasy.org/cellosaurus/CVCL_HQ51

Organism: Homo sapiens (Human)
Disease: Pitt-Hopkins syndrome
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_HQ51 Copy   


  • RRID:CVCL_EH30

https://web.expasy.org/cellosaurus/CVCL_EH30

Organism: Homo sapiens (Human)
Disease: Congenital disorder of deglycosylation
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_EH30 Copy   


  • RRID:CVCL_JF36

https://web.expasy.org/cellosaurus/CVCL_JF36

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

Proper citation: RRID:CVCL_JF36 Copy   


  • RRID:CVCL_JF35

https://web.expasy.org/cellosaurus/CVCL_JF35

Organism: Homo sapiens (Human)
Disease: Potocki-Lupski syndrome
Category: Transformed cell line
Comments:

Proper citation: Coriell Cat# GM25586, RRID:CVCL_JF35 Copy   


  • RRID:CVCL_A5PA

https://web.expasy.org/cellosaurus/CVCL_A5PA

Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_A5PA Copy   


  • RRID:CVCL_A5NP

https://web.expasy.org/cellosaurus/CVCL_A5NP

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

Proper citation: Coriell Cat# GM25858, RRID:CVCL_A5NP Copy   


  • RRID:CVCL_JF41

https://web.expasy.org/cellosaurus/CVCL_JF41

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

Proper citation: RRID:CVCL_JF41 Copy   


  • RRID:CVCL_A5NR

https://web.expasy.org/cellosaurus/CVCL_A5NR

Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_A5NR Copy   


  • RRID:CVCL_A5NU

https://web.expasy.org/cellosaurus/CVCL_A5NU

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; English/German.

Proper citation: Coriell Cat# GM25886, RRID:CVCL_A5NU Copy   


  • RRID:CVCL_A5NW

https://web.expasy.org/cellosaurus/CVCL_A5NW

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

Proper citation: RRID:CVCL_A5NW Copy   


  • RRID:CVCL_VJ19

https://web.expasy.org/cellosaurus/CVCL_VJ19

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

Proper citation: RRID:CVCL_VJ19 Copy   


  • RRID:CVCL_A2VV

https://web.expasy.org/cellosaurus/CVCL_A2VV

Organism: Homo sapiens (Human)
Disease: Central core disease
Category: Transformed cell line
Comments: Population: Caucasian; German.

Proper citation: RRID:CVCL_A2VV Copy   


  • RRID:CVCL_A2VR

https://web.expasy.org/cellosaurus/CVCL_A2VR

Organism: Homo sapiens (Human)
Disease: Central core disease
Category: Transformed cell line
Comments: Population: Caucasian; Dutch/German.

Proper citation: RRID:CVCL_A2VR Copy   


  • RRID:CVCL_A2WC

https://web.expasy.org/cellosaurus/CVCL_A2WC

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

Proper citation: Coriell Cat# GM26182, RRID:CVCL_A2WC Copy   


  • RRID:CVCL_LP09

https://web.expasy.org/cellosaurus/CVCL_LP09

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_LP09 Copy   


  • RRID:CVCL_LH26

https://web.expasy.org/cellosaurus/CVCL_LH26

Organism: Homo sapiens (Human)
Disease: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
Category: Transformed cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_LH26 Copy   


  • RRID:CVCL_RU00

https://web.expasy.org/cellosaurus/CVCL_RU00

Organism: Homo sapiens (Human)
Disease: Central core disease
Category: Transformed cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_RU00 Copy   


  • RRID:CVCL_A2VW

https://web.expasy.org/cellosaurus/CVCL_A2VW

Organism: Homo sapiens (Human)
Disease: Central core disease
Category: Transformed cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM26156, RRID:CVCL_A2VW Copy   


  • RRID:CVCL_A2VM

https://web.expasy.org/cellosaurus/CVCL_A2VM

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

Proper citation: Coriell Cat# GM26131, RRID:CVCL_A2VM Copy   


  • RRID:CVCL_A2WH

https://web.expasy.org/cellosaurus/CVCL_A2WH

Organism: Homo sapiens (Human)
Disease: Pitt-Hopkins syndrome
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_A2WH Copy   



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