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On page 107 showing 2121 ~ 2140 out of 185,176 results
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  • RRID:CVCL_CY27

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_CY27

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

Proper citation: Coriell Cat# GM03313, RRID:CVCL_CY27 Copy   


  • RRID:CVCL_CY27

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_CY27

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

Proper citation: RRID:CVCL_CY27 Copy   


  • RRID:CVCL_J655

https://web.expasy.org/cellosaurus/CVCL_J655

Organism: Homo sapiens (Human)
Disease: Bloom syndrome
Category: Finite cell line
Comments: Donor information: From Bloom Syndrome Registry patient 9(EmSh) (BSR9)., Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_J655 Copy   


  • RRID:CVCL_GT48

https://web.expasy.org/cellosaurus/CVCL_GT48

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

Proper citation: RRID:CVCL_GT48 Copy   


  • RRID:CVCL_V470

https://web.expasy.org/cellosaurus/CVCL_V470

Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XX,der(14;21)(14qter->14q10::21q10->21qter),+21 [34]; 45,XX,der(14;21)(14qter->14q10::21q10->21qter) [16] (Coriell=GM03417)., Population: Caucasian.

Proper citation: RRID:CVCL_V470 Copy   


  • RRID:CVCL_J998

https://web.expasy.org/cellosaurus/CVCL_J998

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

Proper citation: RRID:CVCL_J998 Copy   


  • RRID:CVCL_5M82

https://web.expasy.org/cellosaurus/CVCL_5M82

Organism: Homo sapiens (Human)
Disease: Duchenne muscular dystrophy
Category: Finite cell line
Comments: From: Montreal Children's Hospital cell repository; Montreal; Canada.

Proper citation: RRID:CVCL_5M82 Copy   


  • RRID:CVCL_X285

https://web.expasy.org/cellosaurus/CVCL_X285

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

Proper citation: RRID:CVCL_X285 Copy   


  • RRID:CVCL_7385

https://web.expasy.org/cellosaurus/CVCL_7385

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

Proper citation: RRID:CVCL_7385 Copy   


  • RRID:CVCL_DS12

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_DS12

Organism: Homo sapiens (Human)
Disease: 46,XY sex reversal 1
Category: Finite cell line
Comments: Population: African American.

Proper citation: RRID:CVCL_DS12 Copy   


  • RRID:CVCL_X285

https://web.expasy.org/cellosaurus/CVCL_X285

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

Proper citation: Coriell Cat# GM03369, RRID:CVCL_X285 Copy   


  • RRID:CVCL_1F14

https://web.expasy.org/cellosaurus/CVCL_1F14

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

Proper citation: Coriell Cat# GM03390, RRID:CVCL_1F14 Copy   


  • RRID:CVCL_1F14

https://web.expasy.org/cellosaurus/CVCL_1F14

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

Proper citation: RRID:CVCL_1F14 Copy   


  • RRID:CVCL_W032

https://web.expasy.org/cellosaurus/CVCL_W032

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

Proper citation: RRID:CVCL_W032 Copy   


  • RRID:CVCL_9Z61

https://web.expasy.org/cellosaurus/CVCL_9Z61

Organism: Homo sapiens (Human)
Disease: Neurofibromatosis type 1
Category: Transformed cell line

Proper citation: RRID:CVCL_9Z61 Copy   


  • RRID:CVCL_9Z62

https://web.expasy.org/cellosaurus/CVCL_9Z62

Organism: Homo sapiens (Human)
Disease: Neurofibromatosis type 1
Category: Transformed cell line

Proper citation: Coriell Cat# GM03421, RRID:CVCL_9Z62 Copy   


  • RRID:CVCL_X106

https://web.expasy.org/cellosaurus/CVCL_X106

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 47,XX,inv(9)(pter->p11::q13->p11::q13->qter)pat,+der(22)(22pter->22q11::11q23->11qter)mat (Coriell=GM03371)., Population: African American.

Proper citation: Coriell Cat# GM03371, RRID:CVCL_X106 Copy   


  • RRID:CVCL_0M20

https://web.expasy.org/cellosaurus/CVCL_0M20

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

Proper citation: RRID:CVCL_0M20 Copy   


  • RRID:CVCL_GT49

https://web.expasy.org/cellosaurus/CVCL_GT49

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

Proper citation: RRID:CVCL_GT49 Copy   


  • RRID:CVCL_X105

https://web.expasy.org/cellosaurus/CVCL_X105

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

Proper citation: RRID:CVCL_X105 Copy   



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