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LinkedIn: Outi Kopra | LinkedIn
Outi Kopras berufliches Profil anzeigen LinkedIn ist das weltweit größte professionelle Netzwerk, das Fach- und Führungskräften wie Outi Kopra dabei hilft ...
LinkedIn: Outi Kopra | LinkedIn
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LinkedIn: Outi Kopra | LinkedIn
Senior scientist at Folkhälsan Research Center Expertice: cellular and molecular neurobiology, mouse models, neuronal ceroid lipofuscinoses, progressive myoclonus epilepsy (EPM1) ... Assistant Head Nurse at Helsingin ja Uudenmaan sairaanhoitopiiri - Hospital District of Helsinki and ...
Interests
Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy...
jmg.bmj.com
Outi Kopra,1,2 Anna-Elina Lehesjoki1,2. ABSTRACT. Background The progressive myoclonus epilepsies. (PMEs) comprise a group of clinically and genetically.
Business Profiles
Private Homepages
Outi Kopra's Email - ContactOutcontactout.com › Outi-Kopra
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Outi Kopra's Email and Phone. Senior scientist @ Folkälsan Research Center. Outi Kopra's Email. . View Outi's Contact Info. It's free! Takes
Education
Cln5-deficiency in mice leads to microglial activation, defective...
kclpure.kcl.ac.uk
@article{fdbd91112ffd477da0c74dbab4adbf89,. title = "Cln5-deficiency in mice leads to microglial activation, defective myelination and changes in lipid metabolism",. author = "Mia-Lisa Schmiedt and Tea Blom and Tomas Blom and Outi Kopra and Andrew Wong and {von Schantz-Fant}, Carina and Elina Ikonen and Mervi ...
Books & Literature
Cell signaling research papers - Proteolysis/Ubiquitination ...www.signaling-gateway.org › update › library › proteolysis05
www.signaling-gateway.org
Anna-Kaisa Anttonen, Ibrahim Mahjneh, Riikka H Hämäläinen, Clotilde Lagier-Tourenne, Outi Kopra, Laura Waris, Mikko Anttonen, Tarja Joensuu, Hannu ...
PLOS ONE: Gene Expression Alterations in the Cerebellum and Granule...
journals.plos.org
Outi Kopra. Affiliations Folkhälsan Institute of Genetics, Helsinki, Finland, Department of Medical Genetics, Haartman Institute and Research Programs Unit , Molecular Neurology, University of Helsinki, Helsinki, Finland, Neuroscience Center, University of Helsinki, Helsinki, Finland. Anna-Elina Lehesjoki.
Search Results - Tarja Joensuu
vufind.lboro.ac.uk
Gene expression alterations in the cerebellum and granule neurons of Cstb(-/-) mouse are associated with early synaptic changes and inflammation. by Tarja Joensuu, Saara Tegelberg, Eva Reinmaa, Mikael Segerstråle, Paula Hakala, Heidi Pehkonen, Esa R Korpi, Jaana Tyynelä, Tomi Taira, Iiris Hovatta, Outi Kopra, ...
Movement Disorders: Genetics and Models - Google Books
books.google.de
The use of animal models is a key aspect of scientific research in numerous fields of medicine. Movement Disorders, Second Edition vigorously examines the...
Related Documents
2013 Vlincl lehesjoki
www.slideshare.net
Basic Research on the Neuropathology of CLN8; Variant Late-Infantile Batten Disease
CiteSeerX — BMC Cell Biology BioMed Central
citeseerx.ist.psu.edu
· @MISC{Lyly07bmccell, author = {Annina Lyly and Carina Von Schantz and Tarja Salonen and Outi Kopra and Jani Saarela and Matti Jauhiainen and Aija Kyttälä ...
A mouse model for Finnish variant late infantile neuronal ceroid...
www.deepdyve.com
A mouse model for Finnish variant late infantile. neuronal ceroid lipofuscinosis, CLN5, reveals. neuropathology associated with early aging. Outi Kopra. 1,{.
CiteSeerX — BMC Neuroscience BioMed Central
citeseerx.ist.psu.edu
· @MISC{Lonka05bmcneuroscience, author = {Liina Lonka and Antti Aalto and Outi Kopra and Mervi Kuronen and Zaal Kokaia and Mart Saarma and Anna-elina ...
Scientific Publications
Brain gene expression profiles of Cln1 and Cln5 deficient mice...
bmcgenomics.biomedcentral.com
Outi Kopra 1, 3, 4, Jonathan D Cooper 5, Massimiliano Gentile 2, Iiris Hovatta 1, 6, ... Anu Jalanko 1 Email author; BMC Genomics :146. DOI:
Glycosylation, transport, and complex formation of palmitoyl protein...
bmcmolcellbiol.biomedcentral.com
Annina Lyly, Carina von Schantz, Tarja Salonen, Outi Kopra, Jani Saarela, Matti Jauhiainen, Aija Kyttälä and Anu Jalanko * *
The neuronal ceroid lipofuscinosis Cln8 gene expression is...
bmcneurosci.biomedcentral.com
BMC Neuroscience BMC Neuroscience main menu. About; Articles; Submission Guidelines; Research article. Open Access Outi Kopra 1, 4, Mervi Kuronen 1, 2, …
Publications
Gene Expression Alterations in the Cerebellum and Granule Neurons of...
core.ac.uk
By Tarja Joensuu, Saara Tegelberg, Eva Reinmaa, Mikael Segerstrale, Paula Hakala, Heidi Pehkonen, Esa R. Korpi, Jaana Tyynela, Tomi Taira, Iiris Hovatta, Outi Kopra ...
Brain gene expression profiles of Cln1 and Cln5 deficient mice...
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Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in ... Outi Kopra Affiliated with
Molecular defect of RAPADILINO syndrome expands the phenotype...
www.wikidata.org
scientific article. 0 references. title. Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases (English). 0 references. author · Leena Peltonen-Palotie · series ordinal references. Outi Kopra · series ordinal references. author name string. H Annika Siitonen.
Reports & Statements
MKS1, encoding a component of the flagellar apparatus basal body...
www.nature.com
Brief Communication
Miscellaneous
Outi Kopra | LinkedIn
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View Outi Kopra’s professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Outi Kopra discover inside ...
Outi Kopra | LinkedIn
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Senior scientist at Folkhälsan Research Center PhD: Neurobiology and neuropathology (Alzheimer's disease) ... Expertice: cellular and molecular neurobiology, mouse models, neuronal ceroid lipofuscinoses, progressive myoclonus epilepsy (EPM1)
Stine N Hansen 1,2, Noreen A Alexander 1,2, Carina von Schantz 3,...
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Presentation on theme: "Stine N Hansen 1,2, Noreen A Alexander 1,2, Carina von Schantz 3, Outi Kopra 3, Anu Jalanko 3, Jonathan D Cooper 1,2 Neuropathological and ...
Outi Kopra: free download. Ebooks library. On-line books store on...
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Outi Kopra: free download. Ebooks library. On-line books store on Z-Library | Z-Library. Download books for free. Find books
Neuronal Ceroid- Lipofuscinosis in Two Cats M ARK C HALKLEY – 3 rd Y...
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Case #1Control
mouse model for Finnish variant late infantile neuronal ceroid...
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Outi Kopra 1, †, Jouni Vesa 2, † ‡, Carina von Schantz 1, Tuula Manninen 1, 2
(PDF) Glycosylation, transport, and complex formation of ...www.academia.edu › Glycosylation_transport_and_complex_formation...
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Outi Kopra ... ; Carina von Schantz - ; Tarja Salonen - ; Outi Kopra - ; ...
Autoradiography of GABAA receptors. - Figsharefigshare.com › articles › _Autoradiography_of_GABA_A_receptors_
figshare.com
... Mikael Segerstråle Paula Hakala Heidi Pehkonen Esa R. Korpi Jaana Tyynelä Tomi Taira Iiris Hovatta Outi Kopra Anna-Elina Lehesjoki.
BioMed Central | BMC Neuroscience
egret.psychol.cam.ac.uk
Liina Lonka, Antti Aalto, Outi Kopra, Mervi Kuronen, Zaal Kokaia, Mart Saarma, Anna-Elina Lehesjoki BMC Neuroscience 2005, 6:27 (13 April ...
DataCite Search
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In the E17 mouse embryo, developing gastrointestinal tract (A, B) and DRG (C, D) , hybridized with specific cRNA probe, are shown. Liina Lonka, Antti Aalto, Outi Kopra, Mervi Kuronen, Zaal Kokaia, Mart Saarma & Anna-Elina Lehesjoki. Figure published via Figshare. Copyright information:Taken from "The neuronal ...
Cystatin B Deficiency Sensitizes Neurons to Oxidative Stress in...
www.jneurosci.org
Outi Kopra 1, Tarja Joensuu 1, Paula Hakala 1, Azad Bonni 2, and Anna- Elina Lehesjoki 1; 1 Folkhälsan Institute of Genetics, Department of Medical Genetics and ...
Cln5-deficiency in mice leads to microglial activation, defective...
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Mia-Lisa Schmiedt, Tea Blom, Tomas Blom, Outi Kopra, Andrew Wong, Carina von Schantz-Fant, Elina Ikonen, Mervi Kuronen, Matti Jauhiainen, Jonathan D ...
Deficiency of the INCL protein Ppt1 results in changes in ectopic...
academic.oup.com
Outi Kopra 3, Laurent O. Martinez 4, Kimmo Tanhuanp ää 5, Nisse ...
E-GEOD < Browse < ArrayExpress < EMBL-EBIwww.ebi.ac.uk › arrayexpress › experiments › E-GEOD-3624
www.ebi.ac.uk
EMBL-EBI
Glycosylation, transport, and complex formation of palmitoyl protein...
cyberleninka.org
Similar topics of scientific paper in Biological sciences , author of scholarly article — Annina Lyly, Carina von Schantz, Tarja Salonen, Outi Kopra, Jani Saarela, ...
Hydrolethalus syndrome is caused by a missense mutation in a novel...
academic.oup.com
Lisa Mee 1, †, Heli Honkala 5, †, Outi Kopra 5, 6, Jouni Vesa 1, Saara Finnilä 1
Altmetric – Impaired osteoclast homeostasis in the cystatin...
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Otto Manninen, Tero Puolakkainen, Jemina Lehto, Elina Harittu, Aki Kallonen, Marko Peura, Tiina Laitala-Leinonen, Outi Kopra, Riku Kiviranta, Anna-Elina ...
Marinesco-Sjogren Syndrome - Mito DBmitodb.com › symptoms
mitodb.com
Anna-Kaisa Anttonen, Ibrahim Mahjneh, Riikka H Hämäläinen, Clotilde Lagier-Tourenne, Outi Kopra, Laura Waris, Mikko Anttonen, Tarja Joensuu, Hannu ...
Mouse Model of Unverricht-Lundborg Disease — University of...
researchportal.helsinki.fi
Mouse Model of Unverricht-Lundborg Disease. Outi Kopra, Tarja Joensuu, Anna-Elina Lehesjoki · Neuroscience Center · Research Programs Unit. Research ...
(PDF) Deficiency of the INCL protein Ppt1 results in changes in...
www.academia.edu
Deficiency of the INCL protein Ppt1 results in changes in ectopic F1ATP synthase and altered cholesterol metabolism
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