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On page 64 showing 1261 ~ 1280 out of 20,547 results
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  • RRID:CVCL_2Z51

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

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

Proper citation: RRID:CVCL_2Z51 Copy   


  • RRID:CVCL_0L60

Possibly Discontinued

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

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

Proper citation: RRID:CVCL_0L60 Copy   


  • RRID:CVCL_X307

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

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

Proper citation: RRID:CVCL_X307 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)
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)
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

Proper citation: RRID:CVCL_9R20 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_2T06

https://web.expasy.org/cellosaurus/CVCL_2T06

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;22)(q12;p11) (PubMed=10377420)., Population: Caucasian; Swiss.

Proper citation: Coriell Cat# GM04628, RRID:CVCL_2T06 Copy   


  • RRID:CVCL_7415

https://web.expasy.org/cellosaurus/CVCL_7415

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

Proper citation: RRID:CVCL_7415 Copy   


  • RRID:CVCL_X311

https://web.expasy.org/cellosaurus/CVCL_X311

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

Proper citation: RRID:CVCL_X311 Copy   


  • RRID:CVCL_Y871

https://web.expasy.org/cellosaurus/CVCL_Y871

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

Proper citation: Coriell Cat# GM04723, RRID:CVCL_Y871 Copy   


  • RRID:CVCL_X309

https://web.expasy.org/cellosaurus/CVCL_X309

Organism: Homo sapiens (Human)
Disease: Trisomy 8
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+8 [75]; 46,XX,+8,dic(14;21)(14qter->14p13::21p13->21qter) [25] (Coriell=GM04610).

Proper citation: Coriell Cat# GM04610, RRID:CVCL_X309 Copy   


  • RRID:CVCL_Y797

https://web.expasy.org/cellosaurus/CVCL_Y797

Organism: Homo sapiens (Human)
Disease: Dystrophia myotonica 1
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM04608, RRID:CVCL_Y797 Copy   


  • RRID:CVCL_V474

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_V474

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

Proper citation: RRID:CVCL_V474 Copy   


  • RRID:CVCL_AT05

https://web.expasy.org/cellosaurus/CVCL_AT05

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

Proper citation: Coriell Cat# GM04681, RRID:CVCL_AT05 Copy   


  • RRID:CVCL_Y863

https://web.expasy.org/cellosaurus/CVCL_Y863

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

Proper citation: Coriell Cat# GM04709, RRID:CVCL_Y863 Copy   


  • RRID:CVCL_Y865

https://web.expasy.org/cellosaurus/CVCL_Y865

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

Proper citation: Coriell Cat# GM04715, RRID:CVCL_Y865 Copy   



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