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On page 266 showing 5301 ~ 5320 out of 256,031 results
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  • RRID:CVCL_N011

https://web.expasy.org/cellosaurus/CVCL_N011

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

Proper citation: RRID:CVCL_N011 Copy   


  • RRID:CVCL_1N77

https://web.expasy.org/cellosaurus/CVCL_1N77

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

Proper citation: Coriell Cat# GM03501, RRID:CVCL_1N77 Copy   


  • RRID:CVCL_8B11

https://web.expasy.org/cellosaurus/CVCL_8B11

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

Proper citation: RRID:CVCL_8B11 Copy   


  • RRID:CVCL_X288

https://web.expasy.org/cellosaurus/CVCL_X288

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

Proper citation: RRID:CVCL_X288 Copy   


  • RRID:CVCL_UR71

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_UR71

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

Proper citation: Coriell Cat# GM03527, RRID:CVCL_UR71 Copy   


  • RRID:CVCL_7392

https://web.expasy.org/cellosaurus/CVCL_7392

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

Proper citation: Coriell Cat# GM03524, RRID:CVCL_7392 Copy   


  • RRID:CVCL_U393

https://web.expasy.org/cellosaurus/CVCL_U393

Organism: Homo sapiens (Human)
Disease: Tay-Sachs disease
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_U393 Copy   


  • RRID:CVCL_X293

https://web.expasy.org/cellosaurus/CVCL_X293

Organism: Homo sapiens (Human)
Disease: Trisomy 2
Category: Finite cell line
Comments:

Proper citation: Coriell Cat# GM03576, RRID:CVCL_X293 Copy   


  • RRID:CVCL_UR71

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_UR71

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

Proper citation: RRID:CVCL_UR71 Copy   


  • RRID:CVCL_X291

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_X291

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

Proper citation: RRID:CVCL_X291 Copy   


  • RRID:CVCL_7390

https://web.expasy.org/cellosaurus/CVCL_7390

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Mexican., Part of: Human variation panel.

Proper citation: RRID:CVCL_7390 Copy   


  • RRID:CVCL_F606

https://web.expasy.org/cellosaurus/CVCL_F606

Organism: Homo sapiens (Human)
Disease: Aspartylglycosaminuria
Category: Finite cell line
Comments: Population: African American.

Proper citation: RRID:CVCL_F606 Copy   


  • RRID:CVCL_N010

https://web.expasy.org/cellosaurus/CVCL_N010

Organism: Homo sapiens (Human)
Disease: Tay-Sachs disease
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi., Part of: Human variation panel.

Proper citation: RRID:CVCL_N010 Copy   


  • RRID:CVCL_UR79

https://web.expasy.org/cellosaurus/CVCL_UR79

Organism: Homo sapiens (Human)
Disease: 17-beta-hydroxysteroid dehydrogenase 3 deficiency
Category: Finite cell line
Comments: Population: Arab.

Proper citation: Coriell Cat# GM03547, RRID:CVCL_UR79 Copy   


  • RRID:CVCL_7394

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7394

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

Proper citation: Coriell Cat# GM03529, RRID:CVCL_7394 Copy   


  • RRID:CVCL_X289

https://web.expasy.org/cellosaurus/CVCL_X289

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

Proper citation: RRID:CVCL_X289 Copy   


  • RRID:CVCL_F092

https://web.expasy.org/cellosaurus/CVCL_F092

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

Proper citation: RRID:CVCL_F092 Copy   


  • RRID:CVCL_UT35

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_UT35

Organism: Homo sapiens (Human)
Disease: Gyrate atrophy
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_UT35 Copy   


  • RRID:CVCL_N009

https://web.expasy.org/cellosaurus/CVCL_N009

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;11)(q26;q23) (PubMed=10377420)., Population: Southeast Asian; Vietnamese., Part of: Human variation panel.

Proper citation: Coriell Cat# GM17083, RRID:CVCL_N009 Copy   


  • RRID:CVCL_F088

https://web.expasy.org/cellosaurus/CVCL_F088

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

Proper citation: Coriell Cat# GM03492, RRID:CVCL_F088 Copy   



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