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On page 192 showing 3821 ~ 3840 out of 236,573 results
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  • RRID:CVCL_9R93

https://web.expasy.org/cellosaurus/CVCL_9R93

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

Proper citation: Coriell Cat# GM11407, RRID:CVCL_9R93 Copy   


  • RRID:CVCL_2U07

https://web.expasy.org/cellosaurus/CVCL_2U07

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(8;10)(8qter->8p11.2::10q24->10qter;10pter->10q24::8p11.2->8pter) (Coriell=GM11397).

Proper citation: Coriell Cat# GM11397, RRID:CVCL_2U07 Copy   


  • RRID:CVCL_U533

https://web.expasy.org/cellosaurus/CVCL_U533

Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line

Proper citation: Coriell Cat# GM11388, RRID:CVCL_U533 Copy   


  • RRID:CVCL_9X19

https://web.expasy.org/cellosaurus/CVCL_9X19

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

Proper citation: RRID:CVCL_9X19 Copy   


  • RRID:CVCL_AJ50

https://web.expasy.org/cellosaurus/CVCL_AJ50

Organism: Homo sapiens (Human)
Disease: Hepatocyte nuclear factor 4-alpha associated monogenic diabetes
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.

Proper citation: RRID:CVCL_AJ50 Copy   


  • RRID:CVCL_AJ49

https://web.expasy.org/cellosaurus/CVCL_AJ49

Organism: Homo sapiens (Human)
Disease: Hepatocyte nuclear factor 4-alpha associated monogenic diabetes
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.

Proper citation: RRID:CVCL_AJ49 Copy   


  • RRID:CVCL_9X17

https://web.expasy.org/cellosaurus/CVCL_9X17

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

Proper citation: Coriell Cat# GM11347, RRID:CVCL_9X17 Copy   


  • RRID:CVCL_4F64

https://web.expasy.org/cellosaurus/CVCL_4F64

Organism: Homo sapiens (Human)
Disease: Very long-chain acyl-CoA dehydrogenase deficiency
Category: Finite cell line
Comments: Population: Asian.

Proper citation: RRID:CVCL_4F64 Copy   


  • RRID:CVCL_5P47

https://web.expasy.org/cellosaurus/CVCL_5P47

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

Proper citation: Coriell Cat# GM11389, RRID:CVCL_5P47 Copy   


  • RRID:CVCL_N182

https://web.expasy.org/cellosaurus/CVCL_N182

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Karyotypic information: 49,XYYYY (Coriell=GM11419)., Population: Indian (from Guyana)., Part of: Human variation panel.

Proper citation: RRID:CVCL_N182 Copy   


  • RRID:CVCL_N177

https://web.expasy.org/cellosaurus/CVCL_N177

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Southeast Asian; Khmer Cambodian., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel.

Proper citation: Coriell Cat# GM11377, RRID:CVCL_N177 Copy   


  • RRID:CVCL_9R92

https://web.expasy.org/cellosaurus/CVCL_9R92

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

Proper citation: RRID:CVCL_9R92 Copy   


  • RRID:CVCL_5P48

https://web.expasy.org/cellosaurus/CVCL_5P48

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

Proper citation: Coriell Cat# GM11390, RRID:CVCL_5P48 Copy   


  • RRID:CVCL_N178

https://web.expasy.org/cellosaurus/CVCL_N178

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel.

Proper citation: RRID:CVCL_N178 Copy   


  • RRID:CVCL_U534

https://web.expasy.org/cellosaurus/CVCL_U534

Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line

Proper citation: Coriell Cat# GM11391, RRID:CVCL_U534 Copy   


  • RRID:CVCL_9R92

https://web.expasy.org/cellosaurus/CVCL_9R92

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

Proper citation: Coriell Cat# GM11406, RRID:CVCL_9R92 Copy   


  • RRID:CVCL_AD69

https://web.expasy.org/cellosaurus/CVCL_AD69

Organism: Homo sapiens (Human)
Disease: Maple syrup urine disease
Category: Transformed cell line

Proper citation: Coriell Cat# GM11381, RRID:CVCL_AD69 Copy   


  • RRID:CVCL_1S24

https://web.expasy.org/cellosaurus/CVCL_1S24

Organism: Cricetulus griseus (Chinese hamster)
Category: Hybrid cell line
Comments: Characteristics: Hybrid for chromosome 15 mapping. Contains a complete copy of chromosome 15., Group: Human/rodent somatic cell hybrid.

Proper citation: Coriell Cat# GM11418, RRID:CVCL_1S24 Copy   


  • RRID:CVCL_6E34

https://web.expasy.org/cellosaurus/CVCL_6E34

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

Proper citation: Coriell Cat# GM11431, RRID:CVCL_6E34 Copy   


  • RRID:CVCL_9X18

https://web.expasy.org/cellosaurus/CVCL_9X18

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

Proper citation: RRID:CVCL_9X18 Copy   



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