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On page 18 showing 341 ~ 360 out of 40,100 results
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  • RRID:CVCL_1V13

https://web.expasy.org/cellosaurus/CVCL_1V13

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

Proper citation: Coriell Cat# GM01391, RRID:CVCL_1V13 Copy   


  • RRID:CVCL_4N12

https://web.expasy.org/cellosaurus/CVCL_4N12

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

Proper citation: Coriell Cat# GM01386, RRID:CVCL_4N12 Copy   


  • RRID:CVCL_AV86

https://web.expasy.org/cellosaurus/CVCL_AV86

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

Proper citation: Coriell Cat# GM01406, RRID:CVCL_AV86 Copy   


  • RRID:CVCL_0M09

https://web.expasy.org/cellosaurus/CVCL_0M09

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

Proper citation: Coriell Cat# GM01442, RRID:CVCL_0M09 Copy   


  • RRID:CVCL_7318

https://web.expasy.org/cellosaurus/CVCL_7318

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

Proper citation: Coriell Cat# GM01380, RRID:CVCL_7318 Copy   


  • RRID:CVCL_4N08

https://web.expasy.org/cellosaurus/CVCL_4N08

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

Proper citation: Coriell Cat# GM01354, RRID:CVCL_4N08 Copy   


  • RRID:CVCL_X248

https://web.expasy.org/cellosaurus/CVCL_X248

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

Proper citation: Coriell Cat# GM01441, RRID:CVCL_X248 Copy   


  • RRID:CVCL_DD67

https://web.expasy.org/cellosaurus/CVCL_DD67

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

Proper citation: Coriell Cat# GM01436, RRID:CVCL_DD67 Copy   


  • RRID:CVCL_4N10

https://web.expasy.org/cellosaurus/CVCL_4N10

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

Proper citation: Coriell Cat# GM01377, RRID:CVCL_4N10 Copy   


  • RRID:CVCL_F657

https://web.expasy.org/cellosaurus/CVCL_F657

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

Proper citation: Coriell Cat# GM01416, RRID:CVCL_F657 Copy   


  • RRID:CVCL_X246

https://web.expasy.org/cellosaurus/CVCL_X246

Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,X,der(9)t(X;9)(q34;q12) (PubMed=10377420)., Population: African American.

Proper citation: Coriell Cat# GM01414, RRID:CVCL_X246 Copy   


  • RRID:CVCL_JB82

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JB82

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

Proper citation: Coriell Cat# GM01358, RRID:CVCL_JB82 Copy   


  • RRID:CVCL_H974

https://web.expasy.org/cellosaurus/CVCL_H974

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

Proper citation: Coriell Cat# GM01482, RRID:CVCL_H974 Copy   


  • RRID:CVCL_JD84

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JD84

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

Proper citation: Coriell Cat# GM01534, RRID:CVCL_JD84 Copy   


  • RRID:CVCL_X250

https://web.expasy.org/cellosaurus/CVCL_X250

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

Proper citation: Coriell Cat# GM01535, RRID:CVCL_X250 Copy   


  • RRID:CVCL_X081

https://web.expasy.org/cellosaurus/CVCL_X081

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

Proper citation: Coriell Cat# GM01549, RRID:CVCL_X081 Copy   


  • RRID:CVCL_2H22

https://web.expasy.org/cellosaurus/CVCL_2H22

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

Proper citation: Coriell Cat# GM01558, RRID:CVCL_2H22 Copy   


  • RRID:CVCL_4N17

https://web.expasy.org/cellosaurus/CVCL_4N17

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,rec(3)(qter->p25::q21->qter) [46]; 46,XY,rec(3)(qter->p25::q21->qter),+8 [4] (Coriell=GM01506).

Proper citation: Coriell Cat# GM01506, RRID:CVCL_4N17 Copy   


  • RRID:CVCL_AA15

https://web.expasy.org/cellosaurus/CVCL_AA15

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

Proper citation: Coriell Cat# GM01465, RRID:CVCL_AA15 Copy   


  • RRID:CVCL_V808

https://web.expasy.org/cellosaurus/CVCL_V808

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,t(4;11)(4pter->4q23::11q11->11qter;11pter->11q11::4q23->4qter) [8]; 45,X,t(4;11)(4pter->4q23::11q11->11qter;11pter->11q11::4q23->4qter),add(19)(?::p13.3->qter) [2] (Coriell=GM01561)., Population: Caucasian.

Proper citation: Coriell Cat# GM01561, RRID:CVCL_V808 Copy   



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