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On page 230 showing 4581 ~ 4600 out of 256,031 results
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  • RRID:CVCL_XC51

https://web.expasy.org/cellosaurus/CVCL_XC51

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

Proper citation: RRID:CVCL_XC51 Copy   


  • RRID:CVCL_VV58

https://web.expasy.org/cellosaurus/CVCL_VV58

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; French and Chinese.

Proper citation: RRID:CVCL_VV58 Copy   


  • RRID:CVCL_YN35

https://web.expasy.org/cellosaurus/CVCL_YN35

Organism: Homo sapiens (Human)
Disease: Congenital disorder of glycosylation type Ia
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_YN35 Copy   


  • RRID:CVCL_A2QG

https://web.expasy.org/cellosaurus/CVCL_A2QG

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

Proper citation: Coriell Cat# GM27265, RRID:CVCL_A2QG Copy   


  • RRID:CVCL_A1UL

https://web.expasy.org/cellosaurus/CVCL_A1UL

Organism: Homo sapiens (Human)
Disease: Rett syndrome, congenital variant
Category: Transformed cell line
Comments: Population: Caucasian; German.

Proper citation: Coriell Cat# GM27318, RRID:CVCL_A1UL Copy   


  • RRID:CVCL_A1UW

https://web.expasy.org/cellosaurus/CVCL_A1UW

Organism: Homo sapiens (Human)
Disease: Rett syndrome, congenital variant
Category: Transformed cell line
Comments: Population: Caucasian; Dutch.

Proper citation: RRID:CVCL_A1UW Copy   


  • RRID:CVCL_VV62

https://web.expasy.org/cellosaurus/CVCL_VV62

Organism: Homo sapiens (Human)
Disease: Vici syndrome
Category: Induced pluripotent stem cell
Comments: Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_VV62 Copy   


  • RRID:CVCL_YN41

https://web.expasy.org/cellosaurus/CVCL_YN41

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

Proper citation: Coriell Cat# GM27326, RRID:CVCL_YN41 Copy   


  • RRID:CVCL_YN32

https://web.expasy.org/cellosaurus/CVCL_YN32

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

Proper citation: RRID:CVCL_YN32 Copy   


  • RRID:CVCL_VV57

https://web.expasy.org/cellosaurus/CVCL_VV57

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

Proper citation: RRID:CVCL_VV57 Copy   


  • RRID:CVCL_XC50

https://web.expasy.org/cellosaurus/CVCL_XC50

Organism: Homo sapiens (Human)
Disease: Congenital disorder of deglycosylation
Category: Induced pluripotent stem cell
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_XC50 Copy   


  • RRID:CVCL_YN37

https://web.expasy.org/cellosaurus/CVCL_YN37

Organism: Homo sapiens (Human)
Disease: Developmental and epileptic encephalopathy 25
Category: Transformed cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_YN37 Copy   


  • RRID:CVCL_A1UR

https://web.expasy.org/cellosaurus/CVCL_A1UR

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

Proper citation: RRID:CVCL_A1UR Copy   


  • RRID:CVCL_A1UV

https://web.expasy.org/cellosaurus/CVCL_A1UV

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

Proper citation: RRID:CVCL_A1UV Copy   


  • RRID:CVCL_VV61

https://web.expasy.org/cellosaurus/CVCL_VV61

Organism: Homo sapiens (Human)
Disease: Rett syndrome, congenital variant
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_VV61 Copy   


  • RRID:CVCL_A1UJ

https://web.expasy.org/cellosaurus/CVCL_A1UJ

Organism: Homo sapiens (Human)
Disease: Rett syndrome, congenital variant
Category: Transformed cell line
Comments: Population: Southeast Asian; Thai and Chinese.

Proper citation: RRID:CVCL_A1UJ Copy   


  • RRID:CVCL_VV64

https://web.expasy.org/cellosaurus/CVCL_VV64

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

Proper citation: Coriell Cat# GM27337, RRID:CVCL_VV64 Copy   


  • RRID:CVCL_VV69

https://web.expasy.org/cellosaurus/CVCL_VV69

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

Proper citation: RRID:CVCL_VV69 Copy   


  • RRID:CVCL_A2QC

https://web.expasy.org/cellosaurus/CVCL_A2QC

Organism: Homo sapiens (Human)
Disease: Rett syndrome, congenital variant
Category: Transformed cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM27260, RRID:CVCL_A2QC Copy   


  • RRID:CVCL_UT83

https://web.expasy.org/cellosaurus/CVCL_UT83

Organism: Homo sapiens (Human)
Disease: Rett syndrome, congenital variant
Category: Transformed cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_UT83 Copy   



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