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On page 410 showing 8181 ~ 8200 out of 256,031 results
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  • RRID:CVCL_1S24

https://web.expasy.org/cellosaurus/CVCL_1S24

Organism: Cricetulus griseus (Chinese hamster)
Disease:
Category: Hybrid cell line
Comments: Characteristics: Hybrid for chromosome 15 mapping. Contains a complete copy of chromosome 15., Group: Human/rodent somatic cell hybrid.

Proper citation: RRID:CVCL_1S24 Copy   


  • RRID:CVCL_U534

https://web.expasy.org/cellosaurus/CVCL_U534

Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_U534 Copy   


  • RRID:CVCL_N177

https://web.expasy.org/cellosaurus/CVCL_N177

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

Proper citation: Coriell Cat# GM17088, RRID:CVCL_N177 Copy   


  • RRID:CVCL_N183

https://web.expasy.org/cellosaurus/CVCL_N183

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 49,XYYYY (Coriell=GM11420)., Population: Indian (from Guyana).

Proper citation: Coriell Cat# GM11420, RRID:CVCL_N183 Copy   


  • RRID:CVCL_AV56

https://web.expasy.org/cellosaurus/CVCL_AV56

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; English/German.

Proper citation: Coriell Cat# GM11503, RRID:CVCL_AV56 Copy   


  • RRID:CVCL_Y575

https://web.expasy.org/cellosaurus/CVCL_Y575

Organism: Homo sapiens (Human)
Disease: Infantile neuroaxonal dystrophy
Category: Finite cell line
Comments: Population: Hispanic.

Proper citation: Coriell Cat# GM11529, RRID:CVCL_Y575 Copy   


  • RRID:CVCL_DE46

https://web.expasy.org/cellosaurus/CVCL_DE46

Organism: Homo sapiens (Human)
Disease:
Category: Hybrid cell line
Comments: Group: Human/rodent somatic cell hybrid.

Proper citation: RRID:CVCL_DE46 Copy   


  • RRID:CVCL_4I72

https://web.expasy.org/cellosaurus/CVCL_4I72

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection.

Proper citation: RRID:CVCL_4I72 Copy   


  • RRID:CVCL_JF46

https://web.expasy.org/cellosaurus/CVCL_JF46

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

Proper citation: RRID:CVCL_JF46 Copy   


  • RRID:CVCL_AJ56

https://web.expasy.org/cellosaurus/CVCL_AJ56

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.

Proper citation: RRID:CVCL_AJ56 Copy   


  • RRID:CVCL_AV61

https://web.expasy.org/cellosaurus/CVCL_AV61

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; English.

Proper citation: Coriell Cat# GM11505, RRID:CVCL_AV61 Copy   


  • RRID:CVCL_EG42

https://web.expasy.org/cellosaurus/CVCL_EG42

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Jewish.

Proper citation: Coriell Cat# GM11538, RRID:CVCL_EG42 Copy   


  • RRID:CVCL_0N13

https://web.expasy.org/cellosaurus/CVCL_0N13

Organism: Homo sapiens (Human)
Disease: Cystic fibrosis
Category: Transformed cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_0N13 Copy   


  • RRID:CVCL_AJ56

https://web.expasy.org/cellosaurus/CVCL_AJ56

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.

Proper citation: Coriell Cat# GM11457, RRID:CVCL_AJ56 Copy   


  • RRID:CVCL_1S25

https://web.expasy.org/cellosaurus/CVCL_1S25

Organism: Cricetulus griseus (Chinese hamster)
Disease:
Category: Hybrid cell line
Comments: Group: Human/rodent somatic cell hybrid.

Proper citation: Coriell Cat# GM11543, RRID:CVCL_1S25 Copy   


  • RRID:CVCL_EG41

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_EG41

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

Proper citation: Coriell Cat# GM11537, RRID:CVCL_EG41 Copy   


  • RRID:CVCL_N184

https://web.expasy.org/cellosaurus/CVCL_N184

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

Proper citation: Coriell Cat# GM11532, RRID:CVCL_N184 Copy   


  • RRID:CVCL_4E07

https://web.expasy.org/cellosaurus/CVCL_4E07

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

Proper citation: RRID:CVCL_4E07 Copy   


  • RRID:CVCL_4E08

https://web.expasy.org/cellosaurus/CVCL_4E08

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

Proper citation: RRID:CVCL_4E08 Copy   


  • RRID:CVCL_EG44

https://web.expasy.org/cellosaurus/CVCL_EG44

Organism: Homo sapiens (Human)
Disease: Cockayne syndrome type A
Category: Transformed cell line
Comments: Population: Jewish.

Proper citation: Coriell Cat# GM11540, RRID:CVCL_EG44 Copy   



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