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On page 283 showing 5641 ~ 5660 out of 256,031 results
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  • RRID:CVCL_AW69

https://web.expasy.org/cellosaurus/CVCL_AW69

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

Proper citation: RRID:CVCL_AW69 Copy   


  • RRID:CVCL_X120

https://web.expasy.org/cellosaurus/CVCL_X120

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

Proper citation: RRID:CVCL_X120 Copy   


  • RRID:CVCL_AW69

https://web.expasy.org/cellosaurus/CVCL_AW69

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

Proper citation: Coriell Cat# GM04515, RRID:CVCL_AW69 Copy   


  • RRID:CVCL_AW53

https://web.expasy.org/cellosaurus/CVCL_AW53

Organism: Homo sapiens (Human)
Disease: Dystrophia myotonica 1
Category: Transformed cell line
Comments: Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_AW53 Copy   


  • RRID:CVCL_1I19

https://web.expasy.org/cellosaurus/CVCL_1I19

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection.

Proper citation: RRID:CVCL_1I19 Copy   


  • RRID:CVCL_N019

https://web.expasy.org/cellosaurus/CVCL_N019

Organism: Homo sapiens (Human)
Disease: Phosphoglycerate kinase 1 deficiency
Category: Transformed cell line
Comments: Population: Japanese., Part of: Human variation panel.

Proper citation: Coriell Cat# GM04535, RRID:CVCL_N019 Copy   


  • RRID:CVCL_V567

https://web.expasy.org/cellosaurus/CVCL_V567

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection.

Proper citation: Coriell Cat# GM04479, RRID:CVCL_V567 Copy   


  • RRID:CVCL_2T05

https://web.expasy.org/cellosaurus/CVCL_2T05

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(1;3)(1qter->1p36::3q13.3->3qter;3pter->3q13.3::1p36->1pter) (Coriell=GM04500)., Population: Caucasian.

Proper citation: RRID:CVCL_2T05 Copy   


  • RRID:CVCL_5L51

https://web.expasy.org/cellosaurus/CVCL_5L51

Organism: Homo sapiens (Human)
Disease: Tuberous sclerosis 2
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_5L51 Copy   


  • RRID:CVCL_2Z51

https://web.expasy.org/cellosaurus/CVCL_2Z51

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

Proper citation: RRID:CVCL_2Z51 Copy   


  • RRID:CVCL_0L60

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_0L60

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

Proper citation: RRID:CVCL_0L60 Copy   


  • RRID:CVCL_AA22

https://web.expasy.org/cellosaurus/CVCL_AA22

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

Proper citation: RRID:CVCL_AA22 Copy   


  • RRID:CVCL_X307

https://web.expasy.org/cellosaurus/CVCL_X307

Organism: Homo sapiens (Human)
Disease: Trisomy 16
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_X307 Copy   


  • RRID:CVCL_1I21

https://web.expasy.org/cellosaurus/CVCL_1I21

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease.

Proper citation: RRID:CVCL_1I21 Copy   


  • RRID:CVCL_0M33

https://web.expasy.org/cellosaurus/CVCL_0M33

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

Proper citation: RRID:CVCL_0M33 Copy   


  • RRID:CVCL_V566

https://web.expasy.org/cellosaurus/CVCL_V566

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection.

Proper citation: RRID:CVCL_V566 Copy   


  • RRID:CVCL_0M37

https://web.expasy.org/cellosaurus/CVCL_0M37

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

Proper citation: RRID:CVCL_0M37 Copy   


  • RRID:CVCL_CV41

https://web.expasy.org/cellosaurus/CVCL_CV41

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

Proper citation: Coriell Cat# GM04465, RRID:CVCL_CV41 Copy   


  • RRID:CVCL_F135

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_F135

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Donor information: Established from monozygotic twin of GM04501 (Cellosaurus=CVCL_7409).

Proper citation: Coriell Cat# GM04502, RRID:CVCL_F135 Copy   


  • RRID:CVCL_9R20

https://web.expasy.org/cellosaurus/CVCL_9R20

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

Proper citation: RRID:CVCL_9R20 Copy   



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