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On page 9 showing 161 ~ 180 out of 205 results
Snippet view Table view Download 205 Result(s)
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  • RRID:CVCL_JD89

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JD89

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

Proper citation: RRID:CVCL_JD89 Copy   


  • RRID:CVCL_DE31

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_DE31

Organism: Homo sapiens (Human)
Disease: Cockayne syndrome
Category: Finite cell line

Proper citation: RRID:CVCL_DE31 Copy   


  • RRID:CVCL_DE31

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_DE31

Organism: Homo sapiens (Human)
Disease: Cockayne syndrome
Category: Finite cell line

Proper citation: Coriell Cat# GM01865, RRID:CVCL_DE31 Copy   


  • RRID:CVCL_2U27

https://web.expasy.org/cellosaurus/CVCL_2U27

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

Proper citation: RRID:CVCL_2U27 Copy   


  • RRID:CVCL_LC40

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_LC40

Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line

Proper citation: JCRB Cat# JCRB3045, RRID:CVCL_LC40 Copy   


  • RRID:CVCL_B3MD

https://web.expasy.org/cellosaurus/CVCL_B3MD

Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line

Proper citation: JCRB Cat# JCRB3069, RRID:CVCL_B3MD Copy   


  • RRID:CVCL_B3MD

https://web.expasy.org/cellosaurus/CVCL_B3MD

Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line

Proper citation: RRID:CVCL_B3MD Copy   


  • RRID:CVCL_B3ME

https://web.expasy.org/cellosaurus/CVCL_B3ME

Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line

Proper citation: RRID:CVCL_B3ME Copy   


  • RRID:CVCL_8Y18

https://web.expasy.org/cellosaurus/CVCL_8Y18

Organism: Homo sapiens (Human)
Disease: Russell-Silver syndrome
Category: Transformed cell line
Comments: Population: Caucasian., Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_8Y18 Copy   


  • RRID:CVCL_8Y18

https://web.expasy.org/cellosaurus/CVCL_8Y18

Organism: Homo sapiens (Human)
Disease: Russell-Silver syndrome
Category: Transformed cell line
Comments: Population: Caucasian., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 00102801, RRID:CVCL_8Y18 Copy   


  • RRID:CVCL_5R23

https://web.expasy.org/cellosaurus/CVCL_5R23

Organism: Homo sapiens (Human)
Disease: Isodicentric chromosome
Category: Transformed cell line

Proper citation: Coriell Cat# GM20548, RRID:CVCL_5R23 Copy   


  • RRID:CVCL_5R23

https://web.expasy.org/cellosaurus/CVCL_5R23

Organism: Homo sapiens (Human)
Disease: Isodicentric chromosome
Category: Transformed cell line

Proper citation: RRID:CVCL_5R23 Copy   


  • RRID:CVCL_8W84

https://web.expasy.org/cellosaurus/CVCL_8W84

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_8W84 Copy   


  • RRID:CVCL_8W84

https://web.expasy.org/cellosaurus/CVCL_8W84

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 89030291, RRID:CVCL_8W84 Copy   


  • RRID:CVCL_8X30

https://web.expasy.org/cellosaurus/CVCL_8X30

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Asian., Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_8X30 Copy   


  • RRID:CVCL_8X31

https://web.expasy.org/cellosaurus/CVCL_8X31

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian., Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_8X31 Copy   


  • RRID:CVCL_HL17

https://web.expasy.org/cellosaurus/CVCL_HL17

Organism: Homo sapiens (Human)
Disease: Campomelic dysplasia
Category: Finite cell line

Proper citation: RRID:CVCL_HL17 Copy   


  • RRID:CVCL_RZ81

https://web.expasy.org/cellosaurus/CVCL_RZ81

Organism: Homo sapiens (Human)
Disease: 46,XY gonadal dysgenesis
Category: Transformed cell line

Proper citation: RRID:CVCL_RZ81 Copy   


  • RRID:CVCL_RZ85

https://web.expasy.org/cellosaurus/CVCL_RZ85

Organism: Homo sapiens (Human)
Disease: 46,XY gonadal dysgenesis
Category: Transformed cell line

Proper citation: RRID:CVCL_RZ85 Copy   


  • RRID:CVCL_RZ79

https://web.expasy.org/cellosaurus/CVCL_RZ79

Organism: Homo sapiens (Human)
Disease: 46,XY gonadal dysgenesis
Category: Transformed cell line

Proper citation: JCRB Cat# JCRB1743, RRID:CVCL_RZ79 Copy   



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