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On page 7 showing 121 ~ 140 out of 40,100 results
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  • RRID:CVCL_J995

Discontinued

https://web.expasy.org/cellosaurus/CVCL_J995

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

Proper citation: Coriell Cat# GM00303, RRID:CVCL_J995 Copy   


  • RRID:CVCL_L941

Discontinued

https://web.expasy.org/cellosaurus/CVCL_L941

Organism: Homo sapiens (Human)
Disease: Methylmalonic aciduria, cblA type
Category: Finite cell line

Proper citation: Coriell Cat# GM00051, RRID:CVCL_L941 Copy   


  • RRID:CVCL_W056

https://web.expasy.org/cellosaurus/CVCL_W056

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

Proper citation: Coriell Cat# GM00368, RRID:CVCL_W056 Copy   


  • RRID:CVCL_7278

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_7278

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Senescence: Senesces at 22 PDL (PubMed=6492896)., Population: Caucasian.

Proper citation: Coriell Cat# GM00316, RRID:CVCL_7278 Copy   


  • RRID:CVCL_X229

https://web.expasy.org/cellosaurus/CVCL_X229

Organism: Homo sapiens (Human)
Disease: Isodicentric chromosome
Category: Finite cell line
Comments: Karyotypic information: 45,X [60%]; 46,X,i(X)(p11) [40%] (PubMed=10377420)., Population: Caucasian.

Proper citation: Coriell Cat# GM00339, RRID:CVCL_X229 Copy   


  • RRID:CVCL_7280

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7280

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

Proper citation: Coriell Cat# GM00323, RRID:CVCL_7280 Copy   


  • RRID:CVCL_V766

https://web.expasy.org/cellosaurus/CVCL_V766

Organism: Homo sapiens (Human)
Disease: Wolf-Hirschhorn syndrome
Category: Finite cell line

Proper citation: Coriell Cat# GM00343, RRID:CVCL_V766 Copy   


  • RRID:CVCL_L958

Discontinued

https://web.expasy.org/cellosaurus/CVCL_L958

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

Proper citation: Coriell Cat# GM00318, RRID:CVCL_L958 Copy   


  • RRID:CVCL_0L91

https://web.expasy.org/cellosaurus/CVCL_0L91

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

Proper citation: Coriell Cat# GM00312, RRID:CVCL_0L91 Copy   


  • RRID:CVCL_W057

https://web.expasy.org/cellosaurus/CVCL_W057

Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group A
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM00369, RRID:CVCL_W057 Copy   


  • RRID:CVCL_7277

    This resource has 1+ mentions.

Discontinued

https://web.expasy.org/cellosaurus/CVCL_7277

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

Proper citation: Coriell Cat# GM00075, RRID:CVCL_7277 Copy   


  • RRID:CVCL_1Y42

https://web.expasy.org/cellosaurus/CVCL_1Y42

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

Proper citation: Coriell Cat# GM00294, RRID:CVCL_1Y42 Copy   


  • RRID:CVCL_2N25

https://web.expasy.org/cellosaurus/CVCL_2N25

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

Proper citation: Coriell Cat# GM00403, RRID:CVCL_2N25 Copy   


  • RRID:CVCL_4D77

https://web.expasy.org/cellosaurus/CVCL_4D77

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XY,inv(4)(pter->p14::q2?->p14::q2?->qter)mat (Coriell=GM00413).

Proper citation: Coriell Cat# GM00413, RRID:CVCL_4D77 Copy   


  • RRID:CVCL_H130

https://web.expasy.org/cellosaurus/CVCL_H130

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

Proper citation: Coriell Cat# GM00474, RRID:CVCL_H130 Copy   


  • RRID:CVCL_JD74

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JD74

Organism: Homo sapiens (Human)
Disease: Fanconi anemia
Category: Finite cell line

Proper citation: Coriell Cat# GM00391, RRID:CVCL_JD74 Copy   


  • RRID:CVCL_7287

https://web.expasy.org/cellosaurus/CVCL_7287

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

Proper citation: Coriell Cat# GM00473, RRID:CVCL_7287 Copy   


  • RRID:CVCL_V768

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_V768

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(4;11)(4pter->4q23::11q11->11qter;11pter->11q11::4q23->4qter) (Coriell=GM00380)., Population: Caucasian.

Proper citation: Coriell Cat# GM00380, RRID:CVCL_V768 Copy   


  • RRID:CVCL_V529

https://web.expasy.org/cellosaurus/CVCL_V529

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

Proper citation: Coriell Cat# GM00415, RRID:CVCL_V529 Copy   


  • RRID:CVCL_V769

https://web.expasy.org/cellosaurus/CVCL_V769

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 45,XX,der(13;22)(13qter->13q10::22q10->22qter) (Coriell=GM00392)., Population: Caucasian.

Proper citation: Coriell Cat# GM00392, RRID:CVCL_V769 Copy   



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