PPT-Finding splice sites With particular interest given to the inhibitory dopamine receptor
Author : bethany | Published Date : 2023-07-07
Whats the problem How did I solve it What did I find Would you like to know more Pre mRNA needs to get cut in an ordered fashion So splicing elements cue splicing
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Finding splice sites With particular interest given to the inhibitory dopamine receptor: Transcript
Whats the problem How did I solve it What did I find Would you like to know more Pre mRNA needs to get cut in an ordered fashion So splicing elements cue splicing factors to splice This can be regulatory . Interest in dopamine was intensified by the realisation that dopamine had an important role in the pathogenesis or drug treatment of certain brain History diseases eg Parkinsons disease schizophrenia This lead to much research on the sites of action Synapses are a fundamental part of neural pathways as they regulate decision-making in terms of exciting or inhibiting the post-synaptic neurons. . Review: . Action potentials (AP) reach terminal bud of the pre-synaptic neuron. . Human Physiology D.U. Silverthorn. Pharmacology H.P.Rang, M.M.Dale. Pharmacology G.M.Brenner. Clinical Pharmacology D.R.Laurence. Goodman and Gilman’s The Pharmacology Basis of Therapeutics. British National Formulary(BNF). With particular interest given to the inhibitory dopamine receptor gene (D2). What’s the problem?. How did I solve it?. What did I find?. Would you like to know more?. Pre mRNA needs to get cut in an ordered fashion. Understanding the RNA-Seq evidence tracks on . the GEP UCSC Genome Browser. Wilson Leung. . 08/2016. Introduction to RNA-Seq. RNA-Seq: Massively parallel . RNA. . Seq. uencing using second or third generation sequencing technologies. IN HUMAN TRANSCRIPTOME. Vasily V. Grinev. Associate Professor. Department of Genetics. Faculty of Biology. Belarusian State University. Minsk, Republic of Belarus. DIVERSITY OF SPLICE SITES. IN HUMAN GENOME/TRANSCRIPTOME. Evidence for Adenosine/Dopamine Receptor Interactions: Indications for Heteromerization Rafael Franco, Ph.D., Sergi Ferr 1Boston MA 02115Current PositionTenureEducationColumbia University PhDdegree in pharmacology 2012 Thesis advisor Dr Jonathan A JavitchThesis http//academiccommonscolumbiaedu/catalog/ac3A148832Washingt Schizophrenia. 1. Introduction to neuroanatomy. 2. Organisation of the nervous system. To understand psychiatric disorders, it is important to understand the normal structure and function of the nervous system. BMI/CS 776 . www.biostat.wisc.edu/bmi776/. Spring . 2018. Anthony Gitter. gitter@biostat.wisc.edu. These slides, excluding third-party material, are licensed under . CC BY-NC 4.0. by Mark Craven, Colin Dewey, and Anthony Gitter. Lecture 3. Gene Finding and Sequence Annotation. Objectives of this lecture. Introduce you to basic concepts and approaches of gene finding. Show you differences between gene prediction for prokaryotic and eukaryotic genomes. in three neuronal groups: the the substantia nigra (SN) and the ventral tegmental area (VTA). Dopamine neurons from the SN project predominantly to the dorsal striatum and are mainly concerned with in Nervous System. INTRODUCTION. Function. . Drugs can alter the function of the central nervous system (CNS) to provide. Anticonvulsant effects. Tranquilization (sedation). Analgesia. Page . 1. of 66. Ketamine and PCP . – glutamate receptor antagonists. LSD . – serotonin receptor agonist. Alcohol. – GABA-A and . GABA-B receptor agonist (also NMDA receptor antagonist). MDMA. – increases activity of serotonin, dopamine and noradrenaline by enhancing their release and/or inhibiting reuptake.
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