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On page 104 showing 2061 ~ 2080 out of 95,747 results
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  • RRID:CVCL_1H97

https://web.expasy.org/cellosaurus/CVCL_1H97

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 low risk for disease., Population: Caucasian.

Proper citation: Coriell Cat# GM04203, RRID:CVCL_1H97 Copy   


  • RRID:CVCL_2T02

https://web.expasy.org/cellosaurus/CVCL_2T02

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(4;6)(4pter->4q25::6p25->6pter;6qter->6p25::4q25->4qter) (Coriell=GM04240)., Population: Caucasian.

Proper citation: Coriell Cat# GM04240, RRID:CVCL_2T02 Copy   


  • RRID:CVCL_1H83

https://web.expasy.org/cellosaurus/CVCL_1H83

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(6;19)(6pter->6q13::19p13.3->19pter;19qter->19p13.3::6q13->6qter) [8]; 46,XX,t(7;22)(7qter->7p15::22q13->22qter;22pter->22q13::7p15>-7pter),del(qter->12)(p13) [4]; 46,XX [38] (Coriell=GM04188)., Population: Caucasian.

Proper citation: Coriell Cat# GM04188, RRID:CVCL_1H83 Copy   


  • RRID:CVCL_7407

https://web.expasy.org/cellosaurus/CVCL_7407

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

Proper citation: Coriell Cat# GM04390, RRID:CVCL_7407 Copy   


  • RRID:CVCL_7407

https://web.expasy.org/cellosaurus/CVCL_7407

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

Proper citation: RRID:CVCL_7407 Copy   


  • RRID:CVCL_0M29

https://web.expasy.org/cellosaurus/CVCL_0M29

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

Proper citation: Coriell Cat# GM04338, RRID:CVCL_0M29 Copy   


  • RRID:CVCL_F113

https://web.expasy.org/cellosaurus/CVCL_F113

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_F113 Copy   


  • RRID:CVCL_AY61

https://web.expasy.org/cellosaurus/CVCL_AY61

Organism: Homo sapiens (Human)
Disease: Carbamoyl-phosphate synthetase I deficiency
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_AY61 Copy   


  • RRID:CVCL_GT50

https://web.expasy.org/cellosaurus/CVCL_GT50

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

Proper citation: Coriell Cat# GM04263, RRID:CVCL_GT50 Copy   


  • RRID:CVCL_N016

https://web.expasy.org/cellosaurus/CVCL_N016

Organism: Homo sapiens (Human)
Disease: Intellectual developmental disorder
Category: Finite cell line
Comments: Population: Indian., Part of: Human variation panel.

Proper citation: Coriell Cat# GM04300, RRID:CVCL_N016 Copy   


  • RRID:CVCL_N016

https://web.expasy.org/cellosaurus/CVCL_N016

Organism: Homo sapiens (Human)
Disease: Intellectual developmental disorder
Category: Finite cell line
Comments: Population: Indian., Part of: Human variation panel.

Proper citation: RRID:CVCL_N016 Copy   


  • RRID:CVCL_X304

https://web.expasy.org/cellosaurus/CVCL_X304

Organism: Homo sapiens (Human)
Disease: Intellectual developmental disorder
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+der(22)(22pter->22q11::11q23->11qter)mat (Coriell=GM04370)., Population: Caucasian.

Proper citation: Coriell Cat# GM04370, RRID:CVCL_X304 Copy   


  • RRID:CVCL_N017

https://web.expasy.org/cellosaurus/CVCL_N017

Organism: Homo sapiens (Human)
Disease: Zellweger syndrome
Category: Finite cell line
Comments: Population: Caucasian; Iberian., Part of: Human variation panel.

Proper citation: Coriell Cat# GM04340, RRID:CVCL_N017 Copy   


  • RRID:CVCL_US61

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_US61

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

Proper citation: RRID:CVCL_US61 Copy   


  • RRID:CVCL_5M94

https://web.expasy.org/cellosaurus/CVCL_5M94

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

Proper citation: RRID:CVCL_5M94 Copy   


  • RRID:CVCL_9Y77

https://web.expasy.org/cellosaurus/CVCL_9Y77

Organism: Homo sapiens (Human)
Disease: Albright's hereditary osteodystrophy
Category: Transformed cell line
Comments:

Proper citation: Coriell Cat# GM04411, RRID:CVCL_9Y77 Copy   


  • RRID:CVCL_0M25

https://web.expasy.org/cellosaurus/CVCL_0M25

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

Proper citation: RRID:CVCL_0M25 Copy   


  • RRID:CVCL_0M29

https://web.expasy.org/cellosaurus/CVCL_0M29

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

Proper citation: RRID:CVCL_0M29 Copy   


  • RRID:CVCL_AY61

https://web.expasy.org/cellosaurus/CVCL_AY61

Organism: Homo sapiens (Human)
Disease: Carbamoyl-phosphate synthetase I deficiency
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM04311, RRID:CVCL_AY61 Copy   


  • RRID:CVCL_CZ83

https://web.expasy.org/cellosaurus/CVCL_CZ83

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

Proper citation: Coriell Cat# GM04307, RRID:CVCL_CZ83 Copy   



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