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On page 265 showing 5281 ~ 5300 out of 256,031 results
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  • RRID:CVCL_7392

https://web.expasy.org/cellosaurus/CVCL_7392

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

Proper citation: RRID:CVCL_7392 Copy   


  • RRID:CVCL_JE06

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JE06

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

Proper citation: Coriell Cat# GM03485, RRID:CVCL_JE06 Copy   


  • RRID:CVCL_2Y96

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_2Y96

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_2Y96 Copy   


  • RRID:CVCL_UT35

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_UT35

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

Proper citation: Coriell Cat# GM03540, RRID:CVCL_UT35 Copy   


  • RRID:CVCL_1N77

https://web.expasy.org/cellosaurus/CVCL_1N77

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

Proper citation: RRID:CVCL_1N77 Copy   


  • RRID:CVCL_J658

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_J658

Organism: Homo sapiens (Human)
Disease: Bloom syndrome
Category: Finite cell line
Comments: Donor information: From Bloom Syndrome Registry patient 47(ArSmi) (BSR47).

Proper citation: RRID:CVCL_J658 Copy   


  • RRID:CVCL_X717

https://web.expasy.org/cellosaurus/CVCL_X717

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

Proper citation: RRID:CVCL_X717 Copy   


  • RRID:CVCL_UR75

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_UR75

Organism: Homo sapiens (Human)
Disease: Niemann-Pick disease
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_UR75 Copy   


  • RRID:CVCL_A2PH

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_A2PH

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

Proper citation: RRID:CVCL_A2PH Copy   


  • RRID:CVCL_AD98

https://web.expasy.org/cellosaurus/CVCL_AD98

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

Proper citation: Coriell Cat# GM03521, RRID:CVCL_AD98 Copy   


  • RRID:CVCL_2N31

https://web.expasy.org/cellosaurus/CVCL_2N31

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

Proper citation: RRID:CVCL_2N31 Copy   


  • RRID:CVCL_8B10

https://web.expasy.org/cellosaurus/CVCL_8B10

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

Proper citation: RRID:CVCL_8B10 Copy   


  • RRID:CVCL_N009

https://web.expasy.org/cellosaurus/CVCL_N009

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;11)(q26;q23) (PubMed=10377420)., Population: Southeast Asian; Vietnamese., Part of: Human variation panel.

Proper citation: RRID:CVCL_N009 Copy   


  • RRID:CVCL_F090

https://web.expasy.org/cellosaurus/CVCL_F090

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

Proper citation: RRID:CVCL_F090 Copy   


  • RRID:CVCL_X294

https://web.expasy.org/cellosaurus/CVCL_X294

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Finite cell line
Comments: Karyotypic information: 45,XY,der(3)(3pter->3q29::22q11->22qter),-22 (Coriell=GM03577)., Population: Caucasian.

Proper citation: Coriell Cat# GM03577, RRID:CVCL_X294 Copy   


  • RRID:CVCL_A2PH

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_A2PH

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

Proper citation: Coriell Cat# GM03526, RRID:CVCL_A2PH Copy   


  • RRID:CVCL_X290

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_X290

Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+18 (Coriell=GM03538)., Population: Caucasian.

Proper citation: RRID:CVCL_X290 Copy   


  • RRID:CVCL_7391

https://web.expasy.org/cellosaurus/CVCL_7391

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY [35]; 46,XY,t(3;11)(3pter->3q24::11p15->11pter;11qter->11p15::3q24->3qter) [15] (Coriell=GM03523)., Population: Caucasian.

Proper citation: RRID:CVCL_7391 Copy   


  • RRID:CVCL_AB32

https://web.expasy.org/cellosaurus/CVCL_AB32

Organism: Homo sapiens (Human)
Disease: Triploidy syndrome
Category: Finite cell line
Comments: Karyotypic information: 69,XXY (Coriell=GM03591)., Population: Caucasian.

Proper citation: RRID:CVCL_AB32 Copy   


  • RRID:CVCL_1V20

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_1V20

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

Proper citation: Coriell Cat# GM03495, RRID:CVCL_1V20 Copy   



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