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On page 175 showing 3481 ~ 3500 out of 95,747 results
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  • RRID:CVCL_W618

https://web.expasy.org/cellosaurus/CVCL_W618

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

Proper citation: Coriell Cat# GM13193, RRID:CVCL_W618 Copy   


  • RRID:CVCL_W616

https://web.expasy.org/cellosaurus/CVCL_W616

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

Proper citation: RRID:CVCL_W616 Copy   


  • RRID:CVCL_5F62

https://web.expasy.org/cellosaurus/CVCL_5F62

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

Proper citation: RRID:CVCL_5F62 Copy   


  • RRID:CVCL_U401

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

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

Proper citation: RRID:CVCL_U401 Copy   


  • RRID:CVCL_9Y21

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

Organism: Homo sapiens (Human)
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)
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_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_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

Proper citation: Coriell Cat# GM13243, RRID:CVCL_V394 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)
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_5P73

https://web.expasy.org/cellosaurus/CVCL_5P73

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

Proper citation: Coriell Cat# GM13277, RRID:CVCL_5P73 Copy   


  • RRID:CVCL_4F06

https://web.expasy.org/cellosaurus/CVCL_4F06

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

Proper citation: Coriell Cat# GM13310, RRID:CVCL_4F06 Copy   


  • RRID:CVCL_4F05

https://web.expasy.org/cellosaurus/CVCL_4F05

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

Proper citation: Coriell Cat# GM13309, RRID:CVCL_4F05 Copy   


  • RRID:CVCL_4F09

https://web.expasy.org/cellosaurus/CVCL_4F09

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

Proper citation: RRID:CVCL_4F09 Copy   


  • RRID:CVCL_AX25

https://web.expasy.org/cellosaurus/CVCL_AX25

Organism: Homo sapiens (Human)
Disease: Niemann-Pick disease, type A
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_AX25 Copy   


  • RRID:CVCL_BW64

https://web.expasy.org/cellosaurus/CVCL_BW64

Organism: Homo sapiens (Human)
Disease: D-bifunctional protein deficiency
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_BW64 Copy   


  • RRID:CVCL_1K71

https://web.expasy.org/cellosaurus/CVCL_1K71

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

Proper citation: Coriell Cat# GM13305, RRID:CVCL_1K71 Copy   


  • RRID:CVCL_4F10

https://web.expasy.org/cellosaurus/CVCL_4F10

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

Proper citation: RRID:CVCL_4F10 Copy   



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