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On page 26 showing 501 ~ 520 out of 20,547 results
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  • RRID:CVCL_0R42

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_0R42

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

Proper citation: RRID:CVCL_0R42 Copy   


  • RRID:CVCL_1L23

https://web.expasy.org/cellosaurus/CVCL_1L23

Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type II
Category: Finite cell line
Comments: Population: Bangladeshi.

Proper citation: RRID:CVCL_1L23 Copy   


  • RRID:CVCL_U304

https://web.expasy.org/cellosaurus/CVCL_U304

Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line

Proper citation: RRID:CVCL_U304 Copy   


  • RRID:CVCL_U300

https://web.expasy.org/cellosaurus/CVCL_U300

Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line

Proper citation: RRID:CVCL_U300 Copy   


  • RRID:CVCL_U305

https://web.expasy.org/cellosaurus/CVCL_U305

Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line

Proper citation: RRID:CVCL_U305 Copy   


  • RRID:CVCL_U301

https://web.expasy.org/cellosaurus/CVCL_U301

Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line

Proper citation: RRID:CVCL_U301 Copy   


  • RRID:CVCL_U302

https://web.expasy.org/cellosaurus/CVCL_U302

Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line

Proper citation: RRID:CVCL_U302 Copy   


  • RRID:CVCL_U303

https://web.expasy.org/cellosaurus/CVCL_U303

Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line

Proper citation: RRID:CVCL_U303 Copy   


  • RRID:CVCL_DA99

https://web.expasy.org/cellosaurus/CVCL_DA99

Organism: Homo sapiens (Human)
Disease: Neuronal ceroid lipofuscinosis type 1
Category: Finite cell line

Proper citation: RRID:CVCL_DA99 Copy   


  • RRID:CVCL_GY30

https://web.expasy.org/cellosaurus/CVCL_GY30

Organism: Homo sapiens (Human)
Disease: Molybdenum cofactor deficiency
Category: Finite cell line

Proper citation: Coriell Cat# GM20415, RRID:CVCL_GY30 Copy   


  • RRID:CVCL_GY30

https://web.expasy.org/cellosaurus/CVCL_GY30

Organism: Homo sapiens (Human)
Disease: Molybdenum cofactor deficiency
Category: Finite cell line

Proper citation: RRID:CVCL_GY30 Copy   


  • RRID:CVCL_IM22

https://web.expasy.org/cellosaurus/CVCL_IM22

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: Chimera 46,XX/46,XY., Population: Chinese; Taiwan.

Proper citation: RRID:CVCL_IM22 Copy   


  • RRID:CVCL_IM22

https://web.expasy.org/cellosaurus/CVCL_IM22

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: Chimera 46,XX/46,XY., Population: Chinese; Taiwan.

Proper citation: Coriell Cat# GM20486, RRID:CVCL_IM22 Copy   


  • RRID:CVCL_DS98

https://web.expasy.org/cellosaurus/CVCL_DS98

Organism: Homo sapiens (Human)
Disease: Nephrotic syndrome - NPHS1 associated
Category: Finite cell line

Proper citation: RRID:CVCL_DS98 Copy   


  • RRID:CVCL_AM94

https://web.expasy.org/cellosaurus/CVCL_AM94

Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type III
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi.

Proper citation: Coriell Cat# GM19485, RRID:CVCL_AM94 Copy   


  • RRID:CVCL_AM92

https://web.expasy.org/cellosaurus/CVCL_AM92

Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type III
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_AM92 Copy   


  • RRID:CVCL_AM94

https://web.expasy.org/cellosaurus/CVCL_AM94

Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type III
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_AM94 Copy   


  • RRID:CVCL_1N16

https://web.expasy.org/cellosaurus/CVCL_1N16

Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type IX
Category: Finite cell line

Proper citation: RRID:CVCL_1N16 Copy   


  • RRID:CVCL_1N16

https://web.expasy.org/cellosaurus/CVCL_1N16

Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type IX
Category: Finite cell line

Proper citation: Coriell Cat# GM19647, RRID:CVCL_1N16 Copy   


  • RRID:CVCL_1N18

https://web.expasy.org/cellosaurus/CVCL_1N18

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

Proper citation: Coriell Cat# GM19688, RRID:CVCL_1N18 Copy   



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