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On page 161 showing 3201 ~ 3220 out of 256,031 results
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  • RRID:CVCL_N152

https://web.expasy.org/cellosaurus/CVCL_N152

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: Coriell Cat# GM10647, RRID:CVCL_N152 Copy   


  • RRID:CVCL_1R97

https://web.expasy.org/cellosaurus/CVCL_1R97

Organism: Homo sapiens (Human)
Disease:
Category: Hybrid cell line
Comments: Characteristics: Hybrid for chromosome 17 mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid.

Proper citation: RRID:CVCL_1R97 Copy   


  • RRID:CVCL_UR80

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_UR80

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

Proper citation: Coriell Cat# GM10649, RRID:CVCL_UR80 Copy   


  • RRID:CVCL_DB76

https://web.expasy.org/cellosaurus/CVCL_DB76

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

Proper citation: RRID:CVCL_DB76 Copy   


  • RRID:CVCL_AD73

https://web.expasy.org/cellosaurus/CVCL_AD73

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

Proper citation: Coriell Cat# GM10710, RRID:CVCL_AD73 Copy   


  • RRID:CVCL_V053

https://web.expasy.org/cellosaurus/CVCL_V053

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

Proper citation: RRID:CVCL_V053 Copy   


  • RRID:CVCL_1Y45

https://web.expasy.org/cellosaurus/CVCL_1Y45

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

Proper citation: Coriell Cat# GM10718, RRID:CVCL_1Y45 Copy   


  • RRID:CVCL_0J44

https://web.expasy.org/cellosaurus/CVCL_0J44

Organism: Homo sapiens (Human)
Disease: Primary carnitine deficiency
Category: Finite cell line
Comments: Population: Indian.

Proper citation: RRID:CVCL_0J44 Copy   


  • RRID:CVCL_AJ43

https://web.expasy.org/cellosaurus/CVCL_AJ43

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.

Proper citation: RRID:CVCL_AJ43 Copy   


  • RRID:CVCL_4I28

https://web.expasy.org/cellosaurus/CVCL_4I28

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection.

Proper citation: RRID:CVCL_4I28 Copy   


  • RRID:CVCL_0Q20

https://web.expasy.org/cellosaurus/CVCL_0Q20

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

Proper citation: Coriell Cat# GM10694, RRID:CVCL_0Q20 Copy   


  • RRID:CVCL_4I33

https://web.expasy.org/cellosaurus/CVCL_4I33

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection.

Proper citation: Coriell Cat# GM10708, RRID:CVCL_4I33 Copy   


  • RRID:CVCL_UT33

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_UT33

Organism: Homo sapiens (Human)
Disease: Bloom syndrome
Category: Transformed cell line
Comments: Donor information: From Bloom Syndrome Registry patient 86(NoKi) (BSR86)., Population: Japanese.

Proper citation: RRID:CVCL_UT33 Copy   


  • RRID:CVCL_N153

https://web.expasy.org/cellosaurus/CVCL_N153

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Indian., Part of: Human variation panel.

Proper citation: RRID:CVCL_N153 Copy   


  • RRID:CVCL_2T90

https://web.expasy.org/cellosaurus/CVCL_2T90

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

Proper citation: RRID:CVCL_2T90 Copy   


  • RRID:CVCL_4I27

https://web.expasy.org/cellosaurus/CVCL_4I27

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection.

Proper citation: Coriell Cat# GM10700, RRID:CVCL_4I27 Copy   


  • RRID:CVCL_5P24

https://web.expasy.org/cellosaurus/CVCL_5P24

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

Proper citation: Coriell Cat# GM10709, RRID:CVCL_5P24 Copy   


  • RRID:CVCL_0Q20

https://web.expasy.org/cellosaurus/CVCL_0Q20

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

Proper citation: RRID:CVCL_0Q20 Copy   


  • RRID:CVCL_DB77

https://web.expasy.org/cellosaurus/CVCL_DB77

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

Proper citation: RRID:CVCL_DB77 Copy   


  • RRID:CVCL_AD72

https://web.expasy.org/cellosaurus/CVCL_AD72

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

Proper citation: Coriell Cat# GM10681, RRID:CVCL_AD72 Copy   



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