Difference between revisions of "Model organisms"
From SDMRC
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== Mouse models == | == Mouse models == | ||
| − | Table of mouse models | + | '''''Table of mouse models''''' |
{| class="wikitable sortable" | {| class="wikitable sortable" | ||
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! mouse model !! description !! contact | ! mouse model !! description !! contact | ||
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| − | | Mdx mutation || MDX mutant mice do not express dystrophin and are used as a model system for Duchenne Muscular Dystrophy. || Alessandra Sacco mailto:asacco@sanfordburnham.org | + | | [[Model organisms#Mdx|Mdx mutation]] || MDX mutant mice do not express dystrophin and are used as a model system for Duchenne Muscular Dystrophy. || Alessandra Sacco mailto:asacco@sanfordburnham.org |
|- | |- | ||
| mdx/mTR || MDX mice lacking the RNA component of telomerase (mdx/mTR) have shortened telomeres in muscle cells and severe muscular dystrophy that progressively worsens with age. || Alessandra Sacco mailto:asacco@sanfordburnham.org | | mdx/mTR || MDX mice lacking the RNA component of telomerase (mdx/mTR) have shortened telomeres in muscle cells and severe muscular dystrophy that progressively worsens with age. || Alessandra Sacco mailto:asacco@sanfordburnham.org | ||
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| − | === Mdx mutation === | + | <a name="Mdx">=== Mdx mutation ===</a> |
MDX mutant mice do not express dystrophin and are used as a model system for Duchenne Muscular Dystrophy. <br /> | MDX mutant mice do not express dystrophin and are used as a model system for Duchenne Muscular Dystrophy. <br /> | ||
* More information: [http://jaxmice.jax.org/strain/001801.html More information on the mouse model (JAX lab)]<br /> | * More information: [http://jaxmice.jax.org/strain/001801.html More information on the mouse model (JAX lab)]<br /> | ||
Revision as of 21:56, 10 November 2014
This site contains a list of model organisms to study human myopathies. Please feel free to edit/amend the list.
Mouse models
Table of mouse models
| mouse model | description | contact |
|---|---|---|
| Mdx mutation | MDX mutant mice do not express dystrophin and are used as a model system for Duchenne Muscular Dystrophy. | Alessandra Sacco mailto:asacco@sanfordburnham.org |
| mdx/mTR | MDX mice lacking the RNA component of telomerase (mdx/mTR) have shortened telomeres in muscle cells and severe muscular dystrophy that progressively worsens with age. | Alessandra Sacco mailto:asacco@sanfordburnham.org |
| Obscurin knockout | The obscurin mouse develops a mild skeletal muscle myopathy, characterised by an age-dependent increase in centralised nuclei. | Stephan Lange mailto:slange@ucsd.edu |
<a name="Mdx">=== Mdx mutation ===</a>
MDX mutant mice do not express dystrophin and are used as a model system for Duchenne Muscular Dystrophy.
- More information: More information on the mouse model (JAX lab)
- Human disease: Duchenne Muscular Dystrophy
- Contact: Alessandra Sacco mailto:asacco@sanfordburnham.org
mdx/mTR
MDX mice lacking the RNA component of telomerase (mdx/mTR) have shortened telomeres in muscle cells and severe muscular dystrophy that progressively worsens with age.
- Read the publication here.
- Human disease: Duchenne Muscular Dystrophy
- Contact: Alessandra Sacco mailto:asacco@sanfordburnham.org
Obscurin knockout
The obscurin mouse develops a mild skeletal muscle myopathy, characterised by an age-dependent increase in centralised nuclei.
- Read the publication here or find more information on an SDMRC funded Pilot Projects. More general information on the role of obscurin proteins for muscles can be found here.
- Human disease: Limb-girdle Muscular Dystrophy
- Contact: Stephan Lange mailto:slange@ucsd.edu
