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On page 81 showing 1601 ~ 1620 out of 236,573 results
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  • RRID:CVCL_A9ZH

https://web.expasy.org/cellosaurus/CVCL_A9ZH

Organism: Homo sapiens (Human)
Disease: Neurodegeneration with brain iron accumulation 5
Category: Induced pluripotent stem cell
Comments:

Proper citation: RRID:CVCL_A9ZH Copy   


  • RRID:CVCL_A2YR

https://web.expasy.org/cellosaurus/CVCL_A2YR

Organism: Homo sapiens (Human)
Disease: Leigh disease
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_A2YR Copy   


  • RRID:CVCL_ZW47

https://web.expasy.org/cellosaurus/CVCL_ZW47

Organism: Homo sapiens (Human)
Disease: Cerebral creatine deficiency syndrome 1
Category: Transformed cell line
Comments: Population: Caucasian; British.

Proper citation: RRID:CVCL_ZW47 Copy   


  • RRID:CVCL_A2YV

https://web.expasy.org/cellosaurus/CVCL_A2YV

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

Proper citation: RRID:CVCL_A2YV Copy   


  • RRID:CVCL_ZH99

https://web.expasy.org/cellosaurus/CVCL_ZH99

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

Proper citation: Coriell Cat# GM27864, RRID:CVCL_ZH99 Copy   


  • RRID:CVCL_ZW55

https://web.expasy.org/cellosaurus/CVCL_ZW55

Organism: Homo sapiens (Human)
Disease: Cerebral creatine deficiency syndrome 1
Category: Finite cell line
Comments:

Proper citation: Coriell Cat# GM27889, RRID:CVCL_ZW55 Copy   


  • RRID:CVCL_B0IR

https://web.expasy.org/cellosaurus/CVCL_B0IR

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

Proper citation: RRID:CVCL_B0IR Copy   


  • RRID:CVCL_A5MF

https://web.expasy.org/cellosaurus/CVCL_A5MF

Organism: Homo sapiens (Human)
Disease: Multicentric carpotarsal osteolysis syndrome
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_A5MF Copy   


  • RRID:CVCL_A5MJ

https://web.expasy.org/cellosaurus/CVCL_A5MJ

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

Proper citation: RRID:CVCL_A5MJ Copy   


  • RRID:CVCL_A2TV

https://web.expasy.org/cellosaurus/CVCL_A2TV

Organism: Homo sapiens (Human)
Disease: SLC6A1-associated myoclonic-atonic epilepsy
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_A2TV Copy   


  • RRID:CVCL_A2TR

https://web.expasy.org/cellosaurus/CVCL_A2TR

Organism: Homo sapiens (Human)
Disease: Intellectual developmental disorder, autosomal dominant 9
Category: Induced pluripotent stem cell
Comments:

Proper citation: RRID:CVCL_A2TR Copy   


  • RRID:CVCL_A2YS

https://web.expasy.org/cellosaurus/CVCL_A2YS

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

Proper citation: RRID:CVCL_A2YS Copy   


  • RRID:CVCL_ZW46

https://web.expasy.org/cellosaurus/CVCL_ZW46

Organism: Homo sapiens (Human)
Disease: Cerebral creatine deficiency syndrome 1
Category: Finite cell line
Comments: Population: Caucasian; German.

Proper citation: RRID:CVCL_ZW46 Copy   


  • RRID:CVCL_A2YN

https://web.expasy.org/cellosaurus/CVCL_A2YN

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

Proper citation: Coriell Cat# GM28009, RRID:CVCL_A2YN Copy   


  • RRID:CVCL_A2SS

https://web.expasy.org/cellosaurus/CVCL_A2SS

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

Proper citation: Coriell Cat# GM27873, RRID:CVCL_A2SS Copy   


  • RRID:CVCL_B0I4

https://web.expasy.org/cellosaurus/CVCL_B0I4

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

Proper citation: Coriell Cat# GM28035, RRID:CVCL_B0I4 Copy   


  • RRID:CVCL_A2TF

https://web.expasy.org/cellosaurus/CVCL_A2TF

Organism: Homo sapiens (Human)
Disease: Nemaline myopathy 3
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_A2TF Copy   


  • RRID:CVCL_A2TB

https://web.expasy.org/cellosaurus/CVCL_A2TB

Organism: Homo sapiens (Human)
Disease: Rett syndrome, congenital variant
Category: Induced pluripotent stem cell
Comments:

Proper citation: RRID:CVCL_A2TB Copy   


  • RRID:CVCL_ZW54

https://web.expasy.org/cellosaurus/CVCL_ZW54

Organism: Homo sapiens (Human)
Disease: Cerebral creatine deficiency syndrome 1
Category: Finite cell line
Comments:

Proper citation: Coriell Cat# GM27888, RRID:CVCL_ZW54 Copy   


  • RRID:CVCL_B3SE

https://web.expasy.org/cellosaurus/CVCL_B3SE

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

Proper citation: RRID:CVCL_B3SE Copy   



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