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On page 180 showing 3581 ~ 3600 out of 117,735 results
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  • RRID:CVCL_1Y30

https://web.expasy.org/cellosaurus/CVCL_1Y30

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

Proper citation: RRID:CVCL_1Y30 Copy   


  • RRID:CVCL_4I20

https://web.expasy.org/cellosaurus/CVCL_4I20

Organism: Homo sapiens (Human)
Disease: Depression
Category: Transformed cell line
Comments: Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection.

Proper citation: RRID:CVCL_4I20 Copy   


  • RRID:CVCL_AJ39

https://web.expasy.org/cellosaurus/CVCL_AJ39

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.

Proper citation: Coriell Cat# GM10406, RRID:CVCL_AJ39 Copy   


  • RRID:CVCL_N144

https://web.expasy.org/cellosaurus/CVCL_N144

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection., Part of: Human variation panel.

Proper citation: Coriell Cat# GM10450, RRID:CVCL_N144 Copy   


  • RRID:CVCL_N144

https://web.expasy.org/cellosaurus/CVCL_N144

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection., Part of: Human variation panel.

Proper citation: RRID:CVCL_N144 Copy   


  • RRID:CVCL_EG71

https://web.expasy.org/cellosaurus/CVCL_EG71

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

Proper citation: RRID:CVCL_EG71 Copy   


  • RRID:CVCL_X450

https://web.expasy.org/cellosaurus/CVCL_X450

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

Proper citation: RRID:CVCL_X450 Copy   


  • RRID:CVCL_N356

https://web.expasy.org/cellosaurus/CVCL_N356

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: African; Biaka pygmies., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository.

Proper citation: Coriell Cat# GM10470, RRID:CVCL_N356 Copy   


  • RRID:CVCL_EH06

https://web.expasy.org/cellosaurus/CVCL_EH06

Organism: Homo sapiens (Human)
Disease: Congenital adrenal gland hypoplasia
Category: Transformed cell line
Comments: Population: African American.

Proper citation: Coriell Cat# GM10489, RRID:CVCL_EH06 Copy   


  • RRID:CVCL_4I24

https://web.expasy.org/cellosaurus/CVCL_4I24

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection.

Proper citation: Coriell Cat# GM10513, RRID:CVCL_4I24 Copy   


  • RRID:CVCL_HQ04

https://web.expasy.org/cellosaurus/CVCL_HQ04

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

Proper citation: RRID:CVCL_HQ04 Copy   


  • RRID:CVCL_2T88

https://web.expasy.org/cellosaurus/CVCL_2T88

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(15;19)(15pter->15q13::19q13.3->19qter;19pter->19q13.3::15q13->15qter) (Coriell=GM10635)., Population: Caucasian.

Proper citation: RRID:CVCL_2T88 Copy   


  • RRID:CVCL_AM45

https://web.expasy.org/cellosaurus/CVCL_AM45

Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.

Proper citation: RRID:CVCL_AM45 Copy   


  • RRID:CVCL_DD85

https://web.expasy.org/cellosaurus/CVCL_DD85

Organism: Homo sapiens (Human)
Disease: Hereditary optic atrophy
Category: Finite cell line
Comments: Population: Jewish.

Proper citation: RRID:CVCL_DD85 Copy   


  • RRID:CVCL_5P22

https://web.expasy.org/cellosaurus/CVCL_5P22

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

Proper citation: Coriell Cat# GM10608, RRID:CVCL_5P22 Copy   


  • RRID:CVCL_AM42

https://web.expasy.org/cellosaurus/CVCL_AM42

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.

Proper citation: RRID:CVCL_AM42 Copy   


  • RRID:CVCL_DD84

https://web.expasy.org/cellosaurus/CVCL_DD84

Organism: Homo sapiens (Human)
Disease: Hereditary optic atrophy
Category: Transformed cell line
Comments: Population: Jewish.

Proper citation: RRID:CVCL_DD84 Copy   


  • RRID:CVCL_AM43

https://web.expasy.org/cellosaurus/CVCL_AM43

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.

Proper citation: Coriell Cat# GM10527, RRID:CVCL_AM43 Copy   


  • RRID:CVCL_2T86

https://web.expasy.org/cellosaurus/CVCL_2T86

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

Proper citation: RRID:CVCL_2T86 Copy   


  • RRID:CVCL_4I25

https://web.expasy.org/cellosaurus/CVCL_4I25

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection.

Proper citation: Coriell Cat# GM10514, RRID:CVCL_4I25 Copy   



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