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On page 344 showing 6861 ~ 6880 out of 256,031 results
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  • RRID:CVCL_0R05

https://web.expasy.org/cellosaurus/CVCL_0R05

Organism: Homo sapiens (Human)
Disease: Greig syndrome
Category: Transformed cell line

Proper citation: RRID:CVCL_0R05 Copy   


  • RRID:CVCL_4J01

https://web.expasy.org/cellosaurus/CVCL_4J01

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# GM10511, RRID:CVCL_4J01 Copy   


  • RRID:CVCL_0Q14

https://web.expasy.org/cellosaurus/CVCL_0Q14

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

Proper citation: Coriell Cat# GM10614, RRID:CVCL_0Q14 Copy   


  • RRID:CVCL_5P23

https://web.expasy.org/cellosaurus/CVCL_5P23

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

Proper citation: RRID:CVCL_5P23 Copy   


  • RRID:CVCL_FA39

https://web.expasy.org/cellosaurus/CVCL_FA39

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

Proper citation: RRID:CVCL_FA39 Copy   


  • RRID:CVCL_5P19

https://web.expasy.org/cellosaurus/CVCL_5P19

Organism: Homo sapiens (Human)
Disease: Hypogonadotropic hypogonadism with anosmia
Category: Transformed cell line

Proper citation: Coriell Cat# GM10565, RRID:CVCL_5P19 Copy   


  • RRID:CVCL_N152

https://web.expasy.org/cellosaurus/CVCL_N152

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_N152 Copy   


  • RRID:CVCL_AM49

https://web.expasy.org/cellosaurus/CVCL_AM49

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

Proper citation: RRID:CVCL_AM49 Copy   


  • RRID:CVCL_AM41

https://web.expasy.org/cellosaurus/CVCL_AM41

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

Proper citation: RRID:CVCL_AM41 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: Coriell Cat# GM10624, RRID:CVCL_DD84 Copy   


  • RRID:CVCL_YP32

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_YP32

Organism: Homo sapiens (Human)
Disease: Xeroderma pigmentosum, complementation group D
Category: Transformed cell line

Proper citation: RRID:CVCL_YP32 Copy   


  • RRID:CVCL_N150

https://web.expasy.org/cellosaurus/CVCL_N150

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Pacific., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel.

Proper citation: Coriell Cat# GM17391, RRID:CVCL_N150 Copy   


  • RRID:CVCL_N148

https://web.expasy.org/cellosaurus/CVCL_N148

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Pacific., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel.

Proper citation: Coriell Cat# GM10541, RRID:CVCL_N148 Copy   


  • RRID:CVCL_V345

https://web.expasy.org/cellosaurus/CVCL_V345

Organism: Homo sapiens (Human)
Disease: Bernard-Soulier syndrome
Category: Transformed cell line

Proper citation: RRID:CVCL_V345 Copy   


  • RRID:CVCL_AM50

https://web.expasy.org/cellosaurus/CVCL_AM50

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

Proper citation: RRID:CVCL_AM50 Copy   


  • RRID:CVCL_0Q12

https://web.expasy.org/cellosaurus/CVCL_0Q12

Organism: Homo sapiens (Human)
Disease: Marfan syndrome
Category: Transformed cell line

Proper citation: RRID:CVCL_0Q12 Copy   


  • RRID:CVCL_5P20

https://web.expasy.org/cellosaurus/CVCL_5P20

Organism: Homo sapiens (Human)
Disease: Dyggve-Melchior-Clausen syndrome
Category: Finite cell line
Comments: Population: Pakistani.

Proper citation: RRID:CVCL_5P20 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: Coriell Cat# GM10635, RRID:CVCL_2T88 Copy   


  • RRID:CVCL_0Q16

https://web.expasy.org/cellosaurus/CVCL_0Q16

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

Proper citation: RRID:CVCL_0Q16 Copy   


  • RRID:CVCL_7502

https://web.expasy.org/cellosaurus/CVCL_7502

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Pacific., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel.

Proper citation: Coriell Cat# GM17388, RRID:CVCL_7502 Copy   



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