User:Fehrhart
From WikiPathways
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* ''Location'': Maastricht University and Maastricht University Medical Centre | * ''Location'': Maastricht University and Maastricht University Medical Centre | ||
* ''Professional Interests'': Rare diseases, especially neurological rare diseases, Rett Syndrome, omics data analysis, linked data, tissue engineering, nanoparticle and drug pathways | * ''Professional Interests'': Rare diseases, especially neurological rare diseases, Rett Syndrome, omics data analysis, linked data, tissue engineering, nanoparticle and drug pathways | ||
| + | I hereby elect to apply CC0 to all my contributions to WikiPathways. | ||
Revision as of 10:23, 26 March 2019
| iD | This user has the ORCID identifier: 0000-0002-7770-620X |
Contents |
My WikiPathways
Pathways of Interest
- MECP2 and Associated Rett Syndrome http://www.wikipathways.org/index.php/Pathway:WP3584
- Ciliary landscape https://www.wikipathways.org/index.php/Pathway:WP4352
- Cytosine methylation http://www.wikipathways.org/index.php/Pathway:WP3585
- Valproic acid pathway http://www.wikipathways.org/index.php/Pathway:WP3871
- Cannabinoid receptor signaling http://www.wikipathways.org/index.php/Pathway:WP3869
- Lung fibrosis http://www.wikipathways.org/index.php/Pathway:WP3624
- Lung fibrosis (mouse) https://www.wikipathways.org/index.php/Pathway:WP3632
- Overview of nanoparticle effects http://www.wikipathways.org/index.php/Pathway:WP3287
- Circadian rythm related genes http://www.wikipathways.org/index.php/Pathway:WP3594
- Melatonin metabolism and effects http://www.wikipathways.org/index.php/Pathway:WP3298
- Septum site determination http://www.wikipathways.org/index.php/Pathway:WP3538
- Prader-Willi and Angelman Syndrome https://www.wikipathways.org/index.php/Pathway:WP3998
- Ethanol effects on histone modifications https://www.wikipathways.org/index.php/Pathway:WP3996
- HDAC6 interactions https://www.wikipathways.org/index.php/Pathway:WP3987
- Viral Acute Myocarditis https://www.wikipathways.org/index.php/Pathway:WP4298
- Lamin A-processing pathway https://www.wikipathways.org/index.php/Pathway:WP4299
- The effect of progerin on the involved genes in Hutchinson-Gilford Progeria Syndrome https://www.wikipathways.org/index.php/Pathway:WP4320
- Rett syndrome causing genes https://www.wikipathways.org/index.php/Pathway:WP4312
- Phosphodiesterases in neuronal function https://www.wikipathways.org/index.php/Pathway:WP4222
- Prion disease pathway https://www.wikipathways.org/index.php/Pathway:WP3995
- Olfactory bulb development and olfactory learning https://www.wikipathways.org/index.php/Pathway:WP3609
- Olfactory receptor activity https://www.wikipathways.org/index.php/Pathway:WP3608
- Sleep regulation https://www.wikipathways.org/index.php/Pathway:WP3591
Portals
- Disease
- Rare diseases
- Nanomaterials
Links
- ...
About Me
- Real name: Friederike Ehrhart
- Work: Department of Bioinformatics and GKC-Rett Expertise Centre
- Location: Maastricht University and Maastricht University Medical Centre
- Professional Interests: Rare diseases, especially neurological rare diseases, Rett Syndrome, omics data analysis, linked data, tissue engineering, nanoparticle and drug pathways
I hereby elect to apply CC0 to all my contributions to WikiPathways.
