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On page 172 showing 3421 ~ 3440 out of 236,573 results
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  • RRID:CVCL_AA49

https://web.expasy.org/cellosaurus/CVCL_AA49

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

Proper citation: RRID:CVCL_AA49 Copy   


  • RRID:CVCL_5N00

https://web.expasy.org/cellosaurus/CVCL_5N00

Organism: Homo sapiens (Human)
Disease: Dyggve-Melchior-Clausen syndrome
Category: Finite cell line
Comments: Population: Lebanese.

Proper citation: Coriell Cat# GM04997, RRID:CVCL_5N00 Copy   


  • RRID:CVCL_IJ36

https://web.expasy.org/cellosaurus/CVCL_IJ36

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

Proper citation: Coriell Cat# GM05076, RRID:CVCL_IJ36 Copy   


  • RRID:CVCL_AB35

https://web.expasy.org/cellosaurus/CVCL_AB35

Organism: Homo sapiens (Human)
Disease: Triploidy syndrome
Category: Finite cell line
Comments: Karyotypic information: 69,XXX (Coriell=GM04939)., Population: Caucasian.

Proper citation: Coriell Cat# GM04939, RRID:CVCL_AB35 Copy   


  • RRID:CVCL_V479

https://web.expasy.org/cellosaurus/CVCL_V479

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

Proper citation: RRID:CVCL_V479 Copy   


  • RRID:CVCL_AL00

https://web.expasy.org/cellosaurus/CVCL_AL00

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

Proper citation: RRID:CVCL_AL00 Copy   


  • RRID:CVCL_5N29

https://web.expasy.org/cellosaurus/CVCL_5N29

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

Proper citation: Coriell Cat# GM05173, RRID:CVCL_5N29 Copy   


  • RRID:CVCL_1K27

https://web.expasy.org/cellosaurus/CVCL_1K27

Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth disease type 1A
Category: Transformed cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM05166, RRID:CVCL_1K27 Copy   


  • RRID:CVCL_AW59

https://web.expasy.org/cellosaurus/CVCL_AW59

Organism: Homo sapiens (Human)
Disease: Dystrophia myotonica 1
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_AW59 Copy   


  • RRID:CVCL_DS13

https://web.expasy.org/cellosaurus/CVCL_DS13

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

Proper citation: Coriell Cat# GM05091, RRID:CVCL_DS13 Copy   


  • RRID:CVCL_5N16

https://web.expasy.org/cellosaurus/CVCL_5N16

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

Proper citation: RRID:CVCL_5N16 Copy   


  • RRID:CVCL_AW57

https://web.expasy.org/cellosaurus/CVCL_AW57

Organism: Homo sapiens (Human)
Disease: Dystrophia myotonica 1
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM05142, RRID:CVCL_AW57 Copy   


  • RRID:CVCL_1K23

https://web.expasy.org/cellosaurus/CVCL_1K23

Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth disease type 1A
Category: Transformed cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_1K23 Copy   


  • RRID:CVCL_AA56

https://web.expasy.org/cellosaurus/CVCL_AA56

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

Proper citation: RRID:CVCL_AA56 Copy   


  • RRID:CVCL_5N08

https://web.expasy.org/cellosaurus/CVCL_5N08

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

Proper citation: RRID:CVCL_5N08 Copy   


  • RRID:CVCL_1Q25

https://web.expasy.org/cellosaurus/CVCL_1Q25

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,t(6;7)(6pter->6q21::7q21.2->7qter;7pter->7q21.2::6q21->6qter) (Coriell=GM05184)., Population: Caucasian; Italian.

Proper citation: RRID:CVCL_1Q25 Copy   


  • RRID:CVCL_AX80

https://web.expasy.org/cellosaurus/CVCL_AX80

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

Proper citation: RRID:CVCL_AX80 Copy   


  • RRID:CVCL_5N15

https://web.expasy.org/cellosaurus/CVCL_5N15

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

Proper citation: Coriell Cat# GM05119, RRID:CVCL_5N15 Copy   


  • RRID:CVCL_DD78

https://web.expasy.org/cellosaurus/CVCL_DD78

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

Proper citation: Coriell Cat# GM05181, RRID:CVCL_DD78 Copy   


  • RRID:CVCL_DS13

https://web.expasy.org/cellosaurus/CVCL_DS13

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

Proper citation: RRID:CVCL_DS13 Copy   



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