User:Fehrhart

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Revision as of 10:23, 26 March 2019 (view source) Fehrhart (Talk | contribs) (→About Me) ← Previous diff		Revision as of 10:26, 26 March 2019 (view source) Fehrhart (Talk | contribs) (→Portals) Next diff →
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	== Portals ==		== Portals ==
-	* Disease	+	* Rare diseases [https://www.wikipathways.org/index.php/Portal:RareDisease]
-	* Rare diseases	+	* Disease [https://www.wikipathways.org/index.php/Portal:Disease]
-	* Nanomaterials	+
	== Links ==		== Links ==

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Revision as of 10:26, 26 March 2019

Contents 1 My WikiPathways 2 Pathways of Interest 3 Portals 4 Links 5 About Me

My WikiPathways

• My contributions
• My talk page

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

• Rare diseases [1]
• Disease [2]

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.