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On page 431 showing 8601 ~ 8620 out of 256,031 results
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  • RRID:CVCL_U401

https://web.expasy.org/cellosaurus/CVCL_U401

Organism: Homo sapiens (Human)
Disease: Tay-Sachs disease
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_U401 Copy   


  • RRID:CVCL_9Y21

https://web.expasy.org/cellosaurus/CVCL_9Y21

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Amish., Part of: CEPH/Amish pedigree cell line collection.

Proper citation: Coriell Cat# GM13118, RRID:CVCL_9Y21 Copy   


  • RRID:CVCL_DB84

https://web.expasy.org/cellosaurus/CVCL_DB84

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

Proper citation: Coriell Cat# GM13147, RRID:CVCL_DB84 Copy   


  • RRID:CVCL_9Y33

https://web.expasy.org/cellosaurus/CVCL_9Y33

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

Proper citation: RRID:CVCL_9Y33 Copy   


  • RRID:CVCL_4Z71

https://web.expasy.org/cellosaurus/CVCL_4Z71

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

Proper citation: Coriell Cat# GM13287, RRID:CVCL_4Z71 Copy   


  • RRID:CVCL_2U25

https://web.expasy.org/cellosaurus/CVCL_2U25

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

Proper citation: RRID:CVCL_2U25 Copy   


  • RRID:CVCL_9R32

https://web.expasy.org/cellosaurus/CVCL_9R32

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

Proper citation: RRID:CVCL_9R32 Copy   


  • RRID:CVCL_V395

https://web.expasy.org/cellosaurus/CVCL_V395

Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type Ia
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_V395 Copy   


  • RRID:CVCL_V143

https://web.expasy.org/cellosaurus/CVCL_V143

Organism: Homo sapiens (Human)
Disease: Von Hippel-Lindau syndrome
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_V143 Copy   


  • RRID:CVCL_1S67

https://web.expasy.org/cellosaurus/CVCL_1S67

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

Proper citation: RRID:CVCL_1S67 Copy   


  • RRID:CVCL_4F71

https://web.expasy.org/cellosaurus/CVCL_4F71

Organism: Homo sapiens (Human)
Disease: Medium-chain acyl-CoA dehydrogenase deficiency
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_4F71 Copy   


  • RRID:CVCL_4Z70

https://web.expasy.org/cellosaurus/CVCL_4Z70

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

Proper citation: RRID:CVCL_4Z70 Copy   


  • RRID:CVCL_GZ46

https://web.expasy.org/cellosaurus/CVCL_GZ46

Organism: Homo sapiens (Human)
Disease: Congenital bilateral aplasia of the vas deferens
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_GZ46 Copy   


  • RRID:CVCL_4F07

https://web.expasy.org/cellosaurus/CVCL_4F07

Organism: Homo sapiens (Human)
Disease: Ellis-Van Creveld syndrome
Category: Transformed cell line
Comments: Population: Caucasian; Amish.

Proper citation: RRID:CVCL_4F07 Copy   


  • RRID:CVCL_V394

https://web.expasy.org/cellosaurus/CVCL_V394

Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type Ia
Category: Transformed cell line
Comments:

Proper citation: Coriell Cat# GM13243, RRID:CVCL_V394 Copy   


  • RRID:CVCL_IJ39

https://web.expasy.org/cellosaurus/CVCL_IJ39

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

Proper citation: Coriell Cat# GM13206, RRID:CVCL_IJ39 Copy   


  • RRID:CVCL_4F69

https://web.expasy.org/cellosaurus/CVCL_4F69

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

Proper citation: Coriell Cat# GM13272, RRID:CVCL_4F69 Copy   


  • RRID:CVCL_2U24

https://web.expasy.org/cellosaurus/CVCL_2U24

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(1;13)(1pter->1q25::13q22->13qter;13pter->13q22::1q25->1qter) (Coriell=GM13238).

Proper citation: Coriell Cat# GM13238, RRID:CVCL_2U24 Copy   


  • RRID:CVCL_IJ39

https://web.expasy.org/cellosaurus/CVCL_IJ39

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

Proper citation: RRID:CVCL_IJ39 Copy   


  • RRID:CVCL_V144

https://web.expasy.org/cellosaurus/CVCL_V144

Organism: Homo sapiens (Human)
Disease: Von Hippel-Lindau syndrome
Category: Transformed cell line
Comments:

Proper citation: Coriell Cat# GM13256, RRID:CVCL_V144 Copy   



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