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On page 252 showing 5021 ~ 5040 out of 20,547 results
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  • RRID:CVCL_A5NY

https://web.expasy.org/cellosaurus/CVCL_A5NY

Organism: Homo sapiens (Human)
Disease: Rett syndrome
Category: Finite cell line

Proper citation: RRID:CVCL_A5NY Copy   


  • RRID:CVCL_JF39

https://web.expasy.org/cellosaurus/CVCL_JF39

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

Proper citation: RRID:CVCL_JF39 Copy   


  • RRID:CVCL_EH30

https://web.expasy.org/cellosaurus/CVCL_EH30

Organism: Homo sapiens (Human)
Disease: Congenital disorder of deglycosylation
Category: Finite cell line

Proper citation: RRID:CVCL_EH30 Copy   


  • RRID:CVCL_VJ23

https://web.expasy.org/cellosaurus/CVCL_VJ23

Organism: Homo sapiens (Human)
Disease: Intellectual developmental disorder, autosomal recessive 34
Category: Finite cell line
Comments: Population: Caucasian; Mennonite.

Proper citation: RRID:CVCL_VJ23 Copy   


  • RRID:CVCL_A5NW

https://web.expasy.org/cellosaurus/CVCL_A5NW

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

Proper citation: RRID:CVCL_A5NW Copy   


  • RRID:CVCL_VJ22

https://web.expasy.org/cellosaurus/CVCL_VJ22

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

Proper citation: RRID:CVCL_VJ22 Copy   


  • RRID:CVCL_HK83

https://web.expasy.org/cellosaurus/CVCL_HK83

Organism: Homo sapiens (Human)
Disease: Centronuclear myopathy 1
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_HK83 Copy   


  • RRID:CVCL_VP81

https://web.expasy.org/cellosaurus/CVCL_VP81

Organism: Homo sapiens (Human)
Disease: Lethal neonatal rigidity and multifocal seizure syndrome
Category: Finite cell line
Comments: Population: Caucasian; Amish.

Proper citation: RRID:CVCL_VP81 Copy   


  • RRID:CVCL_HQ53

https://web.expasy.org/cellosaurus/CVCL_HQ53

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

Proper citation: RRID:CVCL_HQ53 Copy   


  • RRID:CVCL_HL69

https://web.expasy.org/cellosaurus/CVCL_HL69

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

Proper citation: RRID:CVCL_HL69 Copy   


  • RRID:CVCL_LH27

https://web.expasy.org/cellosaurus/CVCL_LH27

Organism: Homo sapiens (Human)
Disease: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_LH27 Copy   


  • RRID:CVCL_A2VE

https://web.expasy.org/cellosaurus/CVCL_A2VE

Organism: Homo sapiens (Human)
Disease: Multiple congenital anomalies-hypotonia-seizures syndrome 1
Category: Finite cell line
Comments: Population: Indian.

Proper citation: RRID:CVCL_A2VE Copy   


  • RRID:CVCL_VP82

https://web.expasy.org/cellosaurus/CVCL_VP82

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

Proper citation: RRID:CVCL_VP82 Copy   


  • RRID:CVCL_A2VA

https://web.expasy.org/cellosaurus/CVCL_A2VA

Organism: Homo sapiens (Human)
Disease: Pitt-Hopkins syndrome
Category: Finite cell line
Comments: Population: Caucasian; English.

Proper citation: RRID:CVCL_A2VA Copy   


  • RRID:CVCL_A2VB

https://web.expasy.org/cellosaurus/CVCL_A2VB

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

Proper citation: Coriell Cat# GM26091, RRID:CVCL_A2VB Copy   


  • RRID:CVCL_IU32

https://web.expasy.org/cellosaurus/CVCL_IU32

Organism: Homo sapiens (Human)
Disease: Nemaline myopathy 2
Category: Finite cell line
Comments: Population: Chinese and Jewish; Ashkenazi.

Proper citation: RRID:CVCL_IU32 Copy   


  • RRID:CVCL_LH25

https://web.expasy.org/cellosaurus/CVCL_LH25

Organism: Homo sapiens (Human)
Disease: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_LH25 Copy   


  • RRID:CVCL_YP73

https://web.expasy.org/cellosaurus/CVCL_YP73

Organism: Homo sapiens (Human)
Disease: Nemaline myopathy 2
Category: Finite cell line

Proper citation: RRID:CVCL_YP73 Copy   


  • RRID:CVCL_RT67

https://web.expasy.org/cellosaurus/CVCL_RT67

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

Proper citation: RRID:CVCL_RT67 Copy   


  • RRID:CVCL_VH43

https://web.expasy.org/cellosaurus/CVCL_VH43

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

Proper citation: Coriell Cat# GM27160, RRID:CVCL_VH43 Copy   



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