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On page 355 showing 7081 ~ 7100 out of 95,747 results
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  • RRID:CVCL_C115

https://web.expasy.org/cellosaurus/CVCL_C115

Organism: Homo sapiens (Human)
Category: Embryonic stem cell
Comments: From: University of Washington; Seattle; USA.

Proper citation: RRID:CVCL_C115 Copy   


  • RRID:CVCL_2032

https://web.expasy.org/cellosaurus/CVCL_2032

Organism: Mus musculus (Mouse)
Disease: Mouse erythroid leukemia
Category: Cancer cell line

Proper citation: DSMZ Cat# ACC-44, RRID:CVCL_2032 Copy   


  • RRID:CVCL_2032

https://web.expasy.org/cellosaurus/CVCL_2032

Organism: Mus musculus (Mouse)
Disease: Mouse erythroid leukemia
Category: Cancer cell line

Proper citation: RRID:CVCL_2032 Copy   


  • RRID:CVCL_1196

https://web.expasy.org/cellosaurus/CVCL_1196

Organism: Homo sapiens (Human)
Disease: Childhood chronic myelogenous leukemia, BCR-ABL1 positive
Category: Cancer cell line
Comments: Population: Caucasian., Part of: LL-100 blood cancer cell line panel., Part of: COSMIC cell lines project., Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).

Proper citation: RRID:CVCL_1196 Copy   


  • RRID:CVCL_LC24

https://web.expasy.org/cellosaurus/CVCL_LC24

Organism: Homo sapiens (Human)
Category: Embryonic stem cell
Comments: From: University of Washington; Seattle; USA.

Proper citation: RRID:CVCL_LC24 Copy   


  • RRID:CVCL_A6UI

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_A6UI

Organism: Mus musculus musculus x Mus musculus castaneus (Hybrid house mouse)
Category: Embryonic stem cell
Comments: Karyotypic information: 40,XX, one chromosome X from M.m.musculus and the other from M.m.castaneus (PubMed=10520993).

Proper citation: RRID:CVCL_A6UI Copy   


  • RRID:CVCL_2033

https://web.expasy.org/cellosaurus/CVCL_2033

Organism: Homo sapiens (Human)
Disease: Childhood chronic myelogenous leukemia, BCR-ABL1 positive
Category: Cancer cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_2033 Copy   


  • RRID:CVCL_VR49

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_VR49

Organism: Homo sapiens (Human)
Category: Embryonic stem cell
Comments: Characteristics: Using TALEN two constructs SA-2A-PuroR-Cas9-TRE and SA-2A-Neo-M2rtTA were introduced in the AAVS1 safe harbor locus, one in each allele., Characteristics: Cell line with robust Dox-inducible expression of Cas9. Can be used for rapid and highly efficient generation of biallelic knockout hPSCs for loss-of-function studies.

Proper citation: RRID:CVCL_VR49 Copy   


  • RRID:CVCL_4618

https://web.expasy.org/cellosaurus/CVCL_4618

Organism: Rattus norvegicus (Rat)
Disease: Rat leiomyoma
Category: Cancer cell line

Proper citation: RRID:CVCL_4618 Copy   


  • RRID:CVCL_4620

https://web.expasy.org/cellosaurus/CVCL_4620

Organism: Rattus norvegicus (Rat)
Disease: Rat leiomyoma
Category: Cancer cell line

Proper citation: RRID:CVCL_4620 Copy   


  • RRID:CVCL_4616

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_4616

Organism: Rattus norvegicus (Rat)
Disease: Rat leiomyoma
Category: Cancer cell line

Proper citation: RRID:CVCL_4616 Copy   


  • RRID:CVCL_4W29

https://web.expasy.org/cellosaurus/CVCL_4W29

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

Proper citation: RRID:CVCL_4W29 Copy   


  • RRID:CVCL_EJ61

https://web.expasy.org/cellosaurus/CVCL_EJ61

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

Proper citation: Coriell Cat# GM10078, RRID:CVCL_EJ61 Copy   


  • RRID:CVCL_AM13

https://web.expasy.org/cellosaurus/CVCL_AM13

Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.

Proper citation: RRID:CVCL_AM13 Copy   


  • RRID:CVCL_9X14

https://web.expasy.org/cellosaurus/CVCL_9X14

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

Proper citation: Coriell Cat# GM10082, RRID:CVCL_9X14 Copy   


  • RRID:CVCL_5P10

https://web.expasy.org/cellosaurus/CVCL_5P10

Organism: Homo sapiens (Human)
Disease: Holoprosencephaly
Category: Finite cell line
Comments: Karyotypic information: 46,XX,der(7)(7pter->7q34::13q12.3->13qter)pat (Coriell=GM10064)., Population: Caucasian.

Proper citation: RRID:CVCL_5P10 Copy   


  • RRID:CVCL_AM18

https://web.expasy.org/cellosaurus/CVCL_AM18

Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.

Proper citation: RRID:CVCL_AM18 Copy   


  • RRID:CVCL_AM33

https://web.expasy.org/cellosaurus/CVCL_AM33

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.

Proper citation: RRID:CVCL_AM33 Copy   


  • RRID:CVCL_AJ11

https://web.expasy.org/cellosaurus/CVCL_AJ11

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

Proper citation: RRID:CVCL_AJ11 Copy   


  • RRID:CVCL_AM29

https://web.expasy.org/cellosaurus/CVCL_AM29

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.

Proper citation: RRID:CVCL_AM29 Copy   



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