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On page 80 showing 1581 ~ 1600 out of 185,176 results
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  • RRID:CVCL_2T04

https://web.expasy.org/cellosaurus/CVCL_2T04

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(2;14)(2qter->2p23::14q32->14qter;14pter->14q32::2p23->2pter) (Coriell=GM04410)., Population: Caucasian.

Proper citation: RRID:CVCL_2T04 Copy   


  • RRID:CVCL_GS65

https://web.expasy.org/cellosaurus/CVCL_GS65

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

Proper citation: RRID:CVCL_GS65 Copy   


  • RRID:CVCL_0M23

https://web.expasy.org/cellosaurus/CVCL_0M23

Organism: Homo sapiens (Human)
Disease: Cystic fibrosis
Category: Finite cell line
Comments: Caution: Was originally thought to be homozygous for CFTR p.Phe508del and is still described as such in Coriell., Population: Caucasian.

Proper citation: RRID:CVCL_0M23 Copy   


  • RRID:CVCL_AB34

https://web.expasy.org/cellosaurus/CVCL_AB34

Organism: Homo sapiens (Human)
Disease: Triploidy syndrome
Category: Finite cell line
Comments: Karyotypic information: 69,XXX (Coriell=GM04376)., Population: Caucasian.

Proper citation: RRID:CVCL_AB34 Copy   


  • RRID:CVCL_N017

https://web.expasy.org/cellosaurus/CVCL_N017

Organism: Homo sapiens (Human)
Disease: Zellweger syndrome
Category: Finite cell line
Comments: Population: Caucasian; Iberian., Part of: Human variation panel.

Proper citation: RRID:CVCL_N017 Copy   


  • RRID:CVCL_7406

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_7406

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

Proper citation: Coriell Cat# AG04260, RRID:CVCL_7406 Copy   


  • RRID:CVCL_CZ10

https://web.expasy.org/cellosaurus/CVCL_CZ10

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

Proper citation: RRID:CVCL_CZ10 Copy   


  • RRID:CVCL_V565

https://web.expasy.org/cellosaurus/CVCL_V565

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection.

Proper citation: RRID:CVCL_V565 Copy   


  • RRID:CVCL_X304

https://web.expasy.org/cellosaurus/CVCL_X304

Organism: Homo sapiens (Human)
Disease: Intellectual developmental disorder
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+der(22)(22pter->22q11::11q23->11qter)mat (Coriell=GM04370)., Population: Caucasian.

Proper citation: RRID:CVCL_X304 Copy   


  • RRID:CVCL_2Z44

https://web.expasy.org/cellosaurus/CVCL_2Z44

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

Proper citation: Coriell Cat# GM04329, RRID:CVCL_2Z44 Copy   


  • RRID:CVCL_5M93

https://web.expasy.org/cellosaurus/CVCL_5M93

Organism: Homo sapiens (Human)
Disease: Duchenne muscular dystrophy
Category: Finite cell line
Comments: Population: Caucasian; Sardinian., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_5M93 Copy   


  • RRID:CVCL_AI34

https://web.expasy.org/cellosaurus/CVCL_AI34

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

Proper citation: Coriell Cat# GM04422, RRID:CVCL_AI34 Copy   


  • RRID:CVCL_2T03

https://web.expasy.org/cellosaurus/CVCL_2T03

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(11;22)(11pter->11q23::22q11->22qter;22pter->22q11::11q23->11qter) (Coriell=GM04403)., Population: Caucasian.

Proper citation: Coriell Cat# GM04403, RRID:CVCL_2T03 Copy   


  • RRID:CVCL_2T03

https://web.expasy.org/cellosaurus/CVCL_2T03

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(11;22)(11pter->11q23::22q11->22qter;22pter->22q11::11q23->11qter) (Coriell=GM04403)., Population: Caucasian.

Proper citation: RRID:CVCL_2T03 Copy   


  • RRID:CVCL_0M24

https://web.expasy.org/cellosaurus/CVCL_0M24

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

Proper citation: RRID:CVCL_0M24 Copy   


  • RRID:CVCL_5M91

https://web.expasy.org/cellosaurus/CVCL_5M91

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

Proper citation: Coriell Cat# GM04297, RRID:CVCL_5M91 Copy   


  • RRID:CVCL_AI33

https://web.expasy.org/cellosaurus/CVCL_AI33

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

Proper citation: Coriell Cat# GM04421, RRID:CVCL_AI33 Copy   


  • RRID:CVCL_GS62

https://web.expasy.org/cellosaurus/CVCL_GS62

Organism: Homo sapiens (Human)
Disease: Adenosine deaminase deficiency
Category: Transformed cell line

Proper citation: RRID:CVCL_GS62 Copy   


  • RRID:CVCL_0M31

https://web.expasy.org/cellosaurus/CVCL_0M31

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

Proper citation: RRID:CVCL_0M31 Copy   


  • RRID:CVCL_7406

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_7406

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

Proper citation: RRID:CVCL_7406 Copy   



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