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On page 36 showing 701 ~ 720 out of 10,163 results
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  • RRID:CVCL_7482

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7482

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

Proper citation: Coriell Cat# GM08399, RRID:CVCL_7482 Copy   


  • RRID:CVCL_7481

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7481

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

Proper citation: RRID:CVCL_7481 Copy   


  • RRID:CVCL_7485

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7485

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

Proper citation: RRID:CVCL_7485 Copy   


  • RRID:CVCL_5C55

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_5C55

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: CEPH/Utah pedigree cell line collection.

Proper citation: Coriell Cat# GM11997, RRID:CVCL_5C55 Copy   


  • RRID:CVCL_5C55

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_5C55

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: CEPH/Utah pedigree cell line collection.

Proper citation: RRID:CVCL_5C55 Copy   


  • RRID:CVCL_AY35

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_AY35

Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(1;3)(3pter->3p22::1p32->1qter;1pter->1p32::3p22->3qter) [3]; 46,XY,t(3;12)(3pter->3q12::12q24.1->12qter;12pter->12q24.1:;3q12->3qter) [3]; 46,XY [13] (Coriell=GM09497)., Population: Caucasian.

Proper citation: RRID:CVCL_AY35 Copy   


  • RRID:CVCL_AY35

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_AY35

Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(1;3)(3pter->3p22::1p32->1qter;1pter->1p32::3p22->3qter) [3]; 46,XY,t(3;12)(3pter->3q12::12q24.1->12qter;12pter->12q24.1:;3q12->3qter) [3]; 46,XY [13] (Coriell=GM09497)., Population: Caucasian.

Proper citation: Coriell Cat# GM09497, RRID:CVCL_AY35 Copy   


  • RRID:CVCL_1H73

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_1H73

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

Proper citation: Coriell Cat# GM03868, RRID:CVCL_1H73 Copy   


  • RRID:CVCL_T820

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_T820

Organism: Homo sapiens (Human)
Disease: Friedreich ataxia
Category: Finite cell line
Comments: Caution: Indicated by Coriell to have 420 and 541 GAA repeats., Population: Caucasian.

Proper citation: RRID:CVCL_T820 Copy   


  • RRID:CVCL_V473

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_V473

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

Proper citation: RRID:CVCL_V473 Copy   


  • RRID:CVCL_7413

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7413

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Donor information: Established from monozygotic twin of GM04505 (Cellosaurus=CVCL_7412)., Population: Caucasian.

Proper citation: RRID:CVCL_7413 Copy   


  • RRID:CVCL_7413

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7413

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Donor information: Established from monozygotic twin of GM04505 (Cellosaurus=CVCL_7412)., Population: Caucasian.

Proper citation: Coriell Cat# GM04506, RRID:CVCL_7413 Copy   


  • RRID:CVCL_V475

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_V475

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

Proper citation: Coriell Cat# GM04616, RRID:CVCL_V475 Copy   


  • RRID:CVCL_X310

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_X310

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

Proper citation: Coriell Cat# GM04626, RRID:CVCL_X310 Copy   


  • RRID:CVCL_X310

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_X310

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

Proper citation: RRID:CVCL_X310 Copy   


  • RRID:CVCL_V475

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_V475

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

Proper citation: RRID:CVCL_V475 Copy   


  • RRID:CVCL_AX78

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_AX78

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

Proper citation: RRID:CVCL_AX78 Copy   


  • RRID:CVCL_AX78

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_AX78

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

Proper citation: Coriell Cat# GM05131, RRID:CVCL_AX78 Copy   


  • RRID:CVCL_7432

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7432

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Latino or Hispanic.

Proper citation: RRID:CVCL_7432 Copy   


  • RRID:CVCL_7434

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7434

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

Proper citation: RRID:CVCL_7434 Copy   



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