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On page 245 showing 4881 ~ 4900 out of 256,031 results
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  • RRID:CVCL_1V15

https://web.expasy.org/cellosaurus/CVCL_1V15

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

Proper citation: RRID:CVCL_1V15 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_1Y25

https://web.expasy.org/cellosaurus/CVCL_1Y25

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

Proper citation: RRID:CVCL_1Y25 Copy   


  • RRID:CVCL_V830

https://web.expasy.org/cellosaurus/CVCL_V830

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(1;7)(1qter->1p34::7p13->7pter;7qter->7p13::1p34->1pter) (Coriell=GM01356)., Population: Caucasian.

Proper citation: RRID:CVCL_V830 Copy   


  • RRID:CVCL_X080

https://web.expasy.org/cellosaurus/CVCL_X080

Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments: Karyotypic information: 47,XY,+18.arr(18)x3 (Coriell=GM01359)., Population: Caucasian.

Proper citation: RRID:CVCL_X080 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_2H13

https://web.expasy.org/cellosaurus/CVCL_2H13

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

Proper citation: RRID:CVCL_2H13 Copy   


  • RRID:CVCL_X251

https://web.expasy.org/cellosaurus/CVCL_X251

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

Proper citation: RRID:CVCL_X251 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_M986

https://web.expasy.org/cellosaurus/CVCL_M986

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(5;12)(5pter->5q33::12q24->12qter;12pter->12q24::5q33->5qter) (Coriell=GM01536)., Population: African American., Part of: Human variation panel.

Proper citation: RRID:CVCL_M986 Copy   


  • RRID:CVCL_V214

https://web.expasy.org/cellosaurus/CVCL_V214

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

Proper citation: RRID:CVCL_V214 Copy   


  • RRID:CVCL_2H21

https://web.expasy.org/cellosaurus/CVCL_2H21

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

Proper citation: RRID:CVCL_2H21 Copy   


  • RRID:CVCL_V809

https://web.expasy.org/cellosaurus/CVCL_V809

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 6,XY,rec(13)(pter->q22::p11->pter)pat (Coriell=GM01570).

Proper citation: RRID:CVCL_V809 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_EJ27

https://web.expasy.org/cellosaurus/CVCL_EJ27

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

Proper citation: RRID:CVCL_EJ27 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_X249

https://web.expasy.org/cellosaurus/CVCL_X249

Organism: Homo sapiens (Human)
Disease: Developmental delay
Category: Finite cell line
Comments: Karyotypic information: 46,XY,der(5)(5pter->5q33::6q15->6q25::5q33->5qter)mat (Coriell=GM01524)., Population: African American.

Proper citation: RRID:CVCL_X249 Copy   



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