Publikationer i DiVA Bondeson - Immunologi, genetik och

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Employment Work environment and health Salary and benefits Annual leave, leave of absence and sick leave Professional and careers development Mauno Vihinen har forskat kring varianter i princip under hela sin forskarkarriär. – I min avhandling använde jag protein engineering för att modifiera egenskaper av proteiner. Det är intressant för att förstå sjukdomsmekanismer. Lund OsteoArthritis Division - Nedbrytning av ledbrosk: en biologisk process som leder till artros. Lund Pediatric Rheumatology Research Group. Lund SLE Research Group Mauno Vihinen, BH Belohradsky, RN Haire, E HolinskiFeder, SP Kwan, I Lappalainen et al.

Mauno vihinen

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Posted 10:24 f m by admin. gerd_ahlstroem · rödlök. Lämna ett svar Avbryt svar. Du måste vara inloggad för att skriva en  24 Mar 2020 Mauno Vihinen * How to cite: Vihinen, M. Strategy for Disease Diagnosis, Progression Prediction, Risk Group Stratification and Treatment  Mauno Vihinen. Mauno Vihinen.

For more information contact Prof. Mauno Vihinen ( mauno.vihinen@med.lu.se).

Fjärrinlärning i bioinformatik - Finska Läkaresällskapet

During their maturation, Jouni Väliaho and Mauno Vihinen : The latest publication on Molecular Medicine 2000; 6:(3)155-164 Structural Basis of Bloom Syndrome (BS) Causing Mutations in the BLM Helicase Domain Suo-Bao Rong, Jouni Väliaho, and Mauno Vihinen Full text as HTML and as PDF format. Figures: It has been observed that XLA is caused Vihinen (see Box 1) before publishing their by mutations in all five domains of Btk, Btk-mutation database mutation data to obtain proper PINs and the frequency being approximately pro- An international study group for analysis of prevent any uncertainty about the patient portional to the length of the domain11. Sweden. mauno.vihinen@med.lu.se The establishment of a database has been suggested in order to collect, organize, and distribute genetic information about esophageal cancer.

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oPer-Eric &Marita  Mauno Vihinen och hans medarbetare har utarbetat ett dataprogram som kombinerar fem olika sätt att förutse vad en SNP-variation kan få för  Uddin Kazi, Maria Elfving, Maria Alvarado-Kristensson, Thoas Fioretos, Peter Siesjö, Mauno Vihinen, Alexander Pietras, Jörg Cammenga och Inger Hallström. medicinsk strålningsfysik, Margareta Troein Töllborn, allmänmedicin med särskild inriktning mot professionell utveckling, Mauno Vihinen,  Det menar professor Mauno Vihinen.

Mauno vihinen

Borrow LU card Computers & networks Copying, scanning & printing Study spaces & reading rooms Lockers and trolleys Order digitizations Find your way around Mauno Vihinen 1 Affiliation 1 Department of Experimental Medical Science, Lund University, BMC D10, SE-22184 Lund, Sweden. mauno.vihinen@med.lu.se. PMID: 24533660 PMCID: PMC3931275 DOI: 10.1186/2041-1480-5-9 Abstract Background: Systematic Mauno Vihinen: RASA1base: Database for pathogenic mutations in the RasGAP SH2 domain: Mauno Vihinen: TCIRG1base: Autosomal recessive osteopetrosis (arOP) Mauno Vihinen: Immunodeficiency mutation databases maintained by others (27 databases available) AP3B1: Hermansky-Pudlak syndrome 2 : Home page. FF108 : ATM: Ataxia-telangiectasia : Supervisor: Prof. Mauno Vihinen Reviewers: Prof.
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During their maturation, Jouni Väliaho and Mauno Vihinen : The latest publication on Molecular Medicine 2000; 6:(3)155-164 Structural Basis of Bloom Syndrome (BS) Causing Mutations in the BLM Helicase Domain Suo-Bao Rong, Jouni Väliaho, and Mauno Vihinen Full text as HTML and as PDF format. Figures: It has been observed that XLA is caused Vihinen (see Box 1) before publishing their by mutations in all five domains of Btk, Btk-mutation database mutation data to obtain proper PINs and the frequency being approximately pro- An international study group for analysis of prevent any uncertainty about the patient portional to the length of the domain11. Sweden. mauno.vihinen@med.lu.se The establishment of a database has been suggested in order to collect, organize, and distribute genetic information about esophageal cancer. The World Organization for Specialized Studies on Diseases of the Esophagus and the Human Variome Project will be in … Mauno Vihinen is well-known for his experience and interest in investigating variations and their effects whether they emerge at molecular levels (DNA, RNA protein), in structural context or in the cellular networks and pathways.

Institute of Medical Technology, FIN- 33014 University of Tampere, Finland.
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