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On page 107 showing 2121 ~ 2140 out of 20,547 results
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  • RRID:CVCL_HQ63

https://web.expasy.org/cellosaurus/CVCL_HQ63

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

Proper citation: RRID:CVCL_HQ63 Copy   


  • RRID:CVCL_X281

https://web.expasy.org/cellosaurus/CVCL_X281

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

Proper citation: Coriell Cat# GM03241, RRID:CVCL_X281 Copy   


  • RRID:CVCL_L465

https://web.expasy.org/cellosaurus/CVCL_L465

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

Proper citation: Coriell Cat# GM03177, RRID:CVCL_L465 Copy   


  • RRID:CVCL_4J53

https://web.expasy.org/cellosaurus/CVCL_4J53

Organism: Homo sapiens (Human)
Disease: Glucose-6-phosphate dehydrogenase deficiency
Category: Finite cell line
Comments: Population: Caucasian; Greek.

Proper citation: RRID:CVCL_4J53 Copy   


  • RRID:CVCL_HQ55

https://web.expasy.org/cellosaurus/CVCL_HQ55

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

Proper citation: RRID:CVCL_HQ55 Copy   


  • RRID:CVCL_N004

https://web.expasy.org/cellosaurus/CVCL_N004

Organism: Homo sapiens (Human)
Disease: Glucose-6-phosphate dehydrogenase deficiency
Category: Finite cell line
Comments: Population: Caucasian; Greek., Part of: Human variation panel.

Proper citation: RRID:CVCL_N004 Copy   


  • RRID:CVCL_1U25

https://web.expasy.org/cellosaurus/CVCL_1U25

Organism: Homo sapiens (Human)
Disease: Autosomal dominant torsion dystonia 1
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM03221, RRID:CVCL_1U25 Copy   


  • RRID:CVCL_HQ62

https://web.expasy.org/cellosaurus/CVCL_HQ62

Organism: Homo sapiens (Human)
Disease: Idiopathic torsion dystonia
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_HQ62 Copy   


  • RRID:CVCL_HQ57

https://web.expasy.org/cellosaurus/CVCL_HQ57

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

Proper citation: Coriell Cat# GM03213, RRID:CVCL_HQ57 Copy   


  • RRID:CVCL_1U24

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_1U24

Organism: Homo sapiens (Human)
Disease: Autosomal dominant torsion dystonia 1
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_1U24 Copy   


  • RRID:CVCL_GS60

https://web.expasy.org/cellosaurus/CVCL_GS60

Organism: Homo sapiens (Human)
Disease: Adenosine deaminase deficiency
Category: Finite cell line
Comments: Population: Jewish; Sephardic.

Proper citation: RRID:CVCL_GS60 Copy   


  • RRID:CVCL_HQ60

https://web.expasy.org/cellosaurus/CVCL_HQ60

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

Proper citation: Coriell Cat# GM03216, RRID:CVCL_HQ60 Copy   


  • RRID:CVCL_4D83

https://web.expasy.org/cellosaurus/CVCL_4D83

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

Proper citation: RRID:CVCL_4D83 Copy   


  • RRID:CVCL_V819

https://web.expasy.org/cellosaurus/CVCL_V819

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,inv(5)(pter->p13::q13->p13::q13->qter),t(17;22)(17qter->17p13::22q11->22qter;22pter->22q11::17p13->17pter) (Coriell=GM03196)., Population: Caucasian.

Proper citation: RRID:CVCL_V819 Copy   


  • RRID:CVCL_HQ58

https://web.expasy.org/cellosaurus/CVCL_HQ58

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

Proper citation: RRID:CVCL_HQ58 Copy   


  • RRID:CVCL_V819

https://web.expasy.org/cellosaurus/CVCL_V819

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,inv(5)(pter->p13::q13->p13::q13->qter),t(17;22)(17qter->17p13::22q11->22qter;22pter->22q11::17p13->17pter) (Coriell=GM03196)., Population: Caucasian.

Proper citation: Coriell Cat# GM03196, RRID:CVCL_V819 Copy   


  • RRID:CVCL_9Q84

https://web.expasy.org/cellosaurus/CVCL_9Q84

Organism: Homo sapiens (Human)
Disease: Oculocerebrorenal syndrome
Category: Finite cell line
Comments: Donor information: At sampling donor was not affected with oculocerebrorenal syndrome but has a 50% risk., Population: Caucasian.

Proper citation: RRID:CVCL_9Q84 Copy   


  • RRID:CVCL_N006

https://web.expasy.org/cellosaurus/CVCL_N006

Organism: Homo sapiens (Human)
Disease: Wolman disease
Category: Finite cell line
Comments: Population: Mexican., Part of: Human variation panel.

Proper citation: Coriell Cat# GM03347, RRID:CVCL_N006 Copy   


  • RRID:CVCL_L948

https://web.expasy.org/cellosaurus/CVCL_L948

Organism: Homo sapiens (Human)
Disease: Familial adenomatous polyposis
Category: Finite cell line
Comments: Population: Caucasian; British.

Proper citation: RRID:CVCL_L948 Copy   


  • RRID:CVCL_X282

https://web.expasy.org/cellosaurus/CVCL_X282

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

Proper citation: Coriell Cat# GM03255, RRID:CVCL_X282 Copy   



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