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On page 247 showing 4921 ~ 4940 out of 256,031 results
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  • RRID:CVCL_AA16

https://web.expasy.org/cellosaurus/CVCL_AA16

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

Proper citation: RRID:CVCL_AA16 Copy   


  • RRID:CVCL_AA16

https://web.expasy.org/cellosaurus/CVCL_AA16

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

Proper citation: Coriell Cat# GM01466, RRID:CVCL_AA16 Copy   


  • RRID:CVCL_JD87

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JD87

Organism: Homo sapiens (Human)
Disease: 46,XY gonadal dysgenesis
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_JD87 Copy   


  • RRID:CVCL_X249

https://web.expasy.org/cellosaurus/CVCL_X249

Organism: Homo sapiens (Human)
Disease: Developmental delay
Category: Finite cell line
Comments: Karyotypic information: 46,XY,der(5)(5pter->5q33::6q15->6q25::5q33->5qter)mat (Coriell=GM01524)., Population: African American.

Proper citation: Coriell Cat# GM01524, RRID:CVCL_X249 Copy   


  • RRID:CVCL_1F07

https://web.expasy.org/cellosaurus/CVCL_1F07

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

Proper citation: Coriell Cat# GM01509, RRID:CVCL_1F07 Copy   


  • RRID:CVCL_V213

https://web.expasy.org/cellosaurus/CVCL_V213

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

Proper citation: RRID:CVCL_V213 Copy   


  • RRID:CVCL_GY17

https://web.expasy.org/cellosaurus/CVCL_GY17

Organism: Homo sapiens (Human)
Disease: Cystathioninuria
Category: Transformed cell line
Comments: Karyotypic information: 47,XX,+12 [66%]; 46,XX,-10,+12 [30%]; 45,XX,-10 [4%] (Coriell=GM01566)., Population: Caucasian.

Proper citation: RRID:CVCL_GY17 Copy   


  • RRID:CVCL_H973

https://web.expasy.org/cellosaurus/CVCL_H973

Organism: Homo sapiens (Human)
Disease: Maturity-onset diabetes of the young
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM01486, RRID:CVCL_H973 Copy   


  • RRID:CVCL_1K52

https://web.expasy.org/cellosaurus/CVCL_1K52

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

Proper citation: RRID:CVCL_1K52 Copy   


  • RRID:CVCL_EJ28

https://web.expasy.org/cellosaurus/CVCL_EJ28

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

Proper citation: RRID:CVCL_EJ28 Copy   


  • RRID:CVCL_2Z62

https://web.expasy.org/cellosaurus/CVCL_2Z62

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

Proper citation: Coriell Cat# GM01553, RRID:CVCL_2Z62 Copy   


  • RRID:CVCL_2H20

https://web.expasy.org/cellosaurus/CVCL_2H20

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

Proper citation: Coriell Cat# GM01529, RRID:CVCL_2H20 Copy   


  • RRID:CVCL_9Q88

https://web.expasy.org/cellosaurus/CVCL_9Q88

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

Proper citation: RRID:CVCL_9Q88 Copy   


  • RRID:CVCL_4J36

https://web.expasy.org/cellosaurus/CVCL_4J36

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

Proper citation: RRID:CVCL_4J36 Copy   


  • RRID:CVCL_0P97

https://web.expasy.org/cellosaurus/CVCL_0P97

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(10;21)(10pter->10q26::21q21->21qter;21pter->21q21::10q26->10qter) (Coriell=GM01580)., Population: African American.

Proper citation: RRID:CVCL_0P97 Copy   


  • RRID:CVCL_9Z54

https://web.expasy.org/cellosaurus/CVCL_9Z54

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

Proper citation: RRID:CVCL_9Z54 Copy   


  • RRID:CVCL_AK19

https://web.expasy.org/cellosaurus/CVCL_AK19

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

Proper citation: RRID:CVCL_AK19 Copy   


  • RRID:CVCL_5L41

https://web.expasy.org/cellosaurus/CVCL_5L41

Organism: Homo sapiens (Human)
Disease: Tuberous sclerosis 1
Category: Finite cell line
Comments: Population: African American.

Proper citation: Coriell Cat# GM01637, RRID:CVCL_5L41 Copy   


  • RRID:CVCL_1D24

https://web.expasy.org/cellosaurus/CVCL_1D24

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

Proper citation: Coriell Cat# GM01611, RRID:CVCL_1D24 Copy   


  • RRID:CVCL_5L43

https://web.expasy.org/cellosaurus/CVCL_5L43

Organism: Homo sapiens (Human)
Disease: Tuberous sclerosis 1
Category: Finite cell line
Comments: Population: African American.

Proper citation: RRID:CVCL_5L43 Copy   



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