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On page 390 showing 7781 ~ 7800 out of 256,031 results
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  • RRID:CVCL_2T24

https://web.expasy.org/cellosaurus/CVCL_2T24

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,t(8;15)(8qter->8p23::15q25->15qter;15pter->15q25::8p23->8pter) (Coriell=GM06832)., Population: Caucasian.

Proper citation: RRID:CVCL_2T24 Copy   


  • RRID:CVCL_FA33

https://web.expasy.org/cellosaurus/CVCL_FA33

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

Proper citation: Coriell Cat# GM06830, RRID:CVCL_FA33 Copy   


  • RRID:CVCL_5N52

https://web.expasy.org/cellosaurus/CVCL_5N52

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

Proper citation: Coriell Cat# GM06938, RRID:CVCL_5N52 Copy   


  • RRID:CVCL_UT46

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_UT46

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

Proper citation: RRID:CVCL_UT46 Copy   


  • RRID:CVCL_2Z55

https://web.expasy.org/cellosaurus/CVCL_2Z55

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

Proper citation: RRID:CVCL_2Z55 Copy   


  • RRID:CVCL_AA60

https://web.expasy.org/cellosaurus/CVCL_AA60

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,i(13)(qter->q10::q10->qter) (Coriell=GM06873)., Population: Caucasian.

Proper citation: RRID:CVCL_AA60 Copy   


  • RRID:CVCL_N056

https://web.expasy.org/cellosaurus/CVCL_N056

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: African American., Part of: Human variation panel.

Proper citation: RRID:CVCL_N056 Copy   


  • RRID:CVCL_X458

https://web.expasy.org/cellosaurus/CVCL_X458

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

Proper citation: RRID:CVCL_X458 Copy   


  • RRID:CVCL_UT46

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_UT46

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

Proper citation: Coriell Cat# GM06856, RRID:CVCL_UT46 Copy   


  • RRID:CVCL_AX98

https://web.expasy.org/cellosaurus/CVCL_AX98

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

Proper citation: RRID:CVCL_AX98 Copy   


  • RRID:CVCL_JX32

https://web.expasy.org/cellosaurus/CVCL_JX32

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Donor information: Established from a donor suffering from mental retardation, microcephaly, short stature, hypogonadism, photosensitivity, abnormal neurologic exam and typical skin findings. No defects in DNA repair or replication observed in fibroblasts., Population: Caucasian.

Proper citation: Coriell Cat# GM06934, RRID:CVCL_JX32 Copy   


  • RRID:CVCL_5N52

https://web.expasy.org/cellosaurus/CVCL_5N52

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

Proper citation: RRID:CVCL_5N52 Copy   


  • RRID:CVCL_5N48

https://web.expasy.org/cellosaurus/CVCL_5N48

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+i(18)(pter->p10::p10->pter) (Coriell=GM06871).

Proper citation: Coriell Cat# GM06871, RRID:CVCL_5N48 Copy   


  • RRID:CVCL_UR72

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_UR72

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

Proper citation: RRID:CVCL_UR72 Copy   


  • RRID:CVCL_0F79

https://web.expasy.org/cellosaurus/CVCL_0F79

Organism: Homo sapiens (Human)
Disease:
Category: Hybrid cell line
Comments: Group: Human/rodent somatic cell hybrid.

Proper citation: RRID:CVCL_0F79 Copy   


  • RRID:CVCL_9R48

https://web.expasy.org/cellosaurus/CVCL_9R48

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

Proper citation: RRID:CVCL_9R48 Copy   


  • RRID:CVCL_R578

https://web.expasy.org/cellosaurus/CVCL_R578

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Genome Sample Resource (1000 genomes project) cell lines., Part of: CEPH/Utah pedigree cell line collection.

Proper citation: Coriell Cat# GM06986, RRID:CVCL_R578 Copy   


  • RRID:CVCL_CY46

https://web.expasy.org/cellosaurus/CVCL_CY46

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

Proper citation: RRID:CVCL_CY46 Copy   


  • RRID:CVCL_R581

https://web.expasy.org/cellosaurus/CVCL_R581

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Genome Sample Resource (1000 genomes project) cell lines., Part of: CEPH/Utah pedigree cell line collection.

Proper citation: RRID:CVCL_R581 Copy   


  • RRID:CVCL_5B19

https://web.expasy.org/cellosaurus/CVCL_5B19

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection.

Proper citation: Coriell Cat# GM06988, RRID:CVCL_5B19 Copy   



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