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On page 146 showing 2901 ~ 2920 out of 256,031 results
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  • RRID:CVCL_JB67

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JB67

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

Proper citation: RRID:CVCL_JB67 Copy   


  • RRID:CVCL_4N21

https://web.expasy.org/cellosaurus/CVCL_4N21

Organism: Homo sapiens (Human)
Disease: Autosomal recessive torsion dystonia 2
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_4N21 Copy   


  • RRID:CVCL_1U20

https://web.expasy.org/cellosaurus/CVCL_1U20

Organism: Homo sapiens (Human)
Disease: Autosomal dominant torsion dystonia 1
Category: Transformed cell line
Comments:

Proper citation: Coriell Cat# GM02264, RRID:CVCL_1U20 Copy   


  • RRID:CVCL_9Q90

https://web.expasy.org/cellosaurus/CVCL_9Q90

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

Proper citation: RRID:CVCL_9Q90 Copy   


  • RRID:CVCL_U949

https://web.expasy.org/cellosaurus/CVCL_U949

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

Proper citation: Coriell Cat# GM02228, RRID:CVCL_U949 Copy   


  • RRID:CVCL_2S82

https://web.expasy.org/cellosaurus/CVCL_2S82

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(5;6)(5qter->5p15::6p21->6pter;6qter->6p21::5p15->5pter) (Coriell=GM02426)., Population: Caucasian.

Proper citation: RRID:CVCL_2S82 Copy   


  • RRID:CVCL_H181

https://web.expasy.org/cellosaurus/CVCL_H181

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

Proper citation: RRID:CVCL_H181 Copy   


  • RRID:CVCL_1R62

https://web.expasy.org/cellosaurus/CVCL_1R62

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

Proper citation: RRID:CVCL_1R62 Copy   


  • RRID:CVCL_H183

https://web.expasy.org/cellosaurus/CVCL_H183

Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments:

Proper citation: Coriell Cat# GM02422, RRID:CVCL_H183 Copy   


  • RRID:CVCL_4J51

https://web.expasy.org/cellosaurus/CVCL_4J51

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

Proper citation: RRID:CVCL_4J51 Copy   


  • RRID:CVCL_UY61

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_UY61

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

Proper citation: Coriell Cat# GM02419, RRID:CVCL_UY61 Copy   


  • RRID:CVCL_VE85

https://web.expasy.org/cellosaurus/CVCL_VE85

Organism: Homo sapiens (Human)
Disease: GM1 gangliosidosis
Category: Induced pluripotent stem cell
Comments: Population: Turkish.

Proper citation: RRID:CVCL_VE85 Copy   


  • RRID:CVCL_L749

https://web.expasy.org/cellosaurus/CVCL_L749

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

Proper citation: RRID:CVCL_L749 Copy   


  • RRID:CVCL_L975

Discontinued

https://web.expasy.org/cellosaurus/CVCL_L975

Organism: Homo sapiens (Human)
Disease: Chediak-Higashi syndrome
Category: Transformed cell line
Comments:

Proper citation: Coriell Cat# GM02378, RRID:CVCL_L975 Copy   


  • RRID:CVCL_F267

https://web.expasy.org/cellosaurus/CVCL_F267

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

Proper citation: Coriell Cat# GM02408, RRID:CVCL_F267 Copy   


  • RRID:CVCL_CZ05

https://web.expasy.org/cellosaurus/CVCL_CZ05

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

Proper citation: Coriell Cat# GM02435, RRID:CVCL_CZ05 Copy   


  • RRID:CVCL_GR97

https://web.expasy.org/cellosaurus/CVCL_GR97

Organism: Homo sapiens (Human)
Disease: Type 1 diabetes mellitus
Category: Finite cell line
Comments: Population: Native Central American; Pima.

Proper citation: Coriell Cat# GM02440, RRID:CVCL_GR97 Copy   


  • RRID:CVCL_AA20

https://web.expasy.org/cellosaurus/CVCL_AA20

Organism: Homo sapiens (Human)
Disease: Familial dysautonomia
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_AA20 Copy   


  • RRID:CVCL_IJ35

https://web.expasy.org/cellosaurus/CVCL_IJ35

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

Proper citation: RRID:CVCL_IJ35 Copy   


  • RRID:CVCL_X090

https://web.expasy.org/cellosaurus/CVCL_X090

Organism: Homo sapiens (Human)
Disease: Cri du chat syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XX,del(5)(qter->p14) (Coriell=GM02337)., Population: Caucasian.

Proper citation: RRID:CVCL_X090 Copy   



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