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On page 413 showing 8241 ~ 8260 out of 20,547 results
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  • RRID:CVCL_C7WF

https://web.expasy.org/cellosaurus/CVCL_C7WF

Organism: Equus asinus (Donkey)
Category: Finite cell line
Comments: Miscellaneous: As no cell line name was provided in the paper, we assigned the name based on the abbreviation of the cell line description.

Proper citation: RRID:CVCL_C7WF Copy   


  • RRID:CVCL_C9IC

https://web.expasy.org/cellosaurus/CVCL_C9IC

Organism: Homo sapiens (Human)
Disease: Parkinson disease 6, early onset
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_C9IC Copy   


  • RRID:CVCL_C8FD

https://web.expasy.org/cellosaurus/CVCL_C8FD

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

Proper citation: RRID:CVCL_C8FD Copy   


  • RRID:CVCL_D3AC

https://web.expasy.org/cellosaurus/CVCL_D3AC

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

Proper citation: RRID:CVCL_D3AC Copy   


  • RRID:CVCL_D2ZC

https://web.expasy.org/cellosaurus/CVCL_D2ZC

Organism: Homo sapiens (Human)
Disease: Multiple mitochondrial dysfunctions syndrome type 3
Category: Finite cell line
Comments: Population: Mexican.

Proper citation: RRID:CVCL_D2ZC Copy   


  • RRID:CVCL_D3AG

https://web.expasy.org/cellosaurus/CVCL_D3AG

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

Proper citation: RRID:CVCL_D3AG Copy   


  • RRID:CVCL_D3AL

https://web.expasy.org/cellosaurus/CVCL_D3AL

Organism: Homo sapiens (Human)
Disease: Developmental and epileptic encephalopathy 85 with or without midline brain defects
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_D3AL Copy   


  • RRID:CVCL_D2ZY

https://web.expasy.org/cellosaurus/CVCL_D2ZY

Organism: Homo sapiens (Human)
Disease: Spastic paraplegia 4
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_D2ZY Copy   


  • RRID:CVCL_D2ZU

https://web.expasy.org/cellosaurus/CVCL_D2ZU

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Southeast Asian; Vietnamese.

Proper citation: RRID:CVCL_D2ZU Copy   


  • RRID:CVCL_D2ZQ

https://web.expasy.org/cellosaurus/CVCL_D2ZQ

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

Proper citation: RRID:CVCL_D2ZQ Copy   


  • RRID:CVCL_D3AK

https://web.expasy.org/cellosaurus/CVCL_D3AK

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

Proper citation: RRID:CVCL_D3AK Copy   


  • RRID:CVCL_C8CQ

https://web.expasy.org/cellosaurus/CVCL_C8CQ

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Characteristics: CD105low/CD26high fibroblasts (Ximbio=153784).

Proper citation: RRID:CVCL_C8CQ Copy   


  • RRID:CVCL_C0LY

https://web.expasy.org/cellosaurus/CVCL_C0LY

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

Proper citation: Coriell Cat# GM28388, RRID:CVCL_C0LY Copy   


  • RRID:CVCL_C0LM

https://web.expasy.org/cellosaurus/CVCL_C0LM

Organism: Homo sapiens (Human)
Disease: Neurodegeneration with brain iron accumulation 5
Category: Finite cell line
Comments: Population: Caucasian; Finnish/German.

Proper citation: RRID:CVCL_C0LM Copy   


  • RRID:CVCL_C0NX

https://web.expasy.org/cellosaurus/CVCL_C0NX

Organism: Homo sapiens (Human)
Disease: GM1 gangliosidosis
Category: Finite cell line
Comments: Population: Japanese.

Proper citation: RRID:CVCL_C0NX Copy   


  • RRID:CVCL_C0LU

https://web.expasy.org/cellosaurus/CVCL_C0LU

Organism: Homo sapiens (Human)
Disease: Ataxia-pancytopenia syndrome
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_C0LU Copy   


  • RRID:CVCL_C0M0

https://web.expasy.org/cellosaurus/CVCL_C0M0

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

Proper citation: Coriell Cat# GM28390, RRID:CVCL_C0M0 Copy   


  • RRID:CVCL_C0LQ

https://web.expasy.org/cellosaurus/CVCL_C0LQ

Organism: Homo sapiens (Human)
Disease: Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy
Category: Finite cell line
Comments: Population: Latino or Hispanic.

Proper citation: RRID:CVCL_C0LQ Copy   


  • RRID:CVCL_C0LY

https://web.expasy.org/cellosaurus/CVCL_C0LY

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

Proper citation: RRID:CVCL_C0LY Copy   


  • RRID:CVCL_C0LH

https://web.expasy.org/cellosaurus/CVCL_C0LH

Organism: Homo sapiens (Human)
Disease: Neurodegeneration with brain iron accumulation 5
Category: Finite cell line
Comments: Population: Caucasian; German/Irish.

Proper citation: RRID:CVCL_C0LH Copy   



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