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Elulookirjeldus (CV)
1.Eesnimi Andres
2.Perekonnanimi Veske
3.Töökoht Tallinna Tehnikaülikool, Geenitehnoloogia Instituut, Molekulaarbioloogia õppetool
4.Ametikoht dotsent
5.Sünniaeg 04.07.1965 (päev.kuu.aasta)
6.Haridus Tallinna 43.Keskkool, 1983. a. Tartu Ülikool, Bioloogia-geograafiateaduskond, rakubioloog 1991. a.
7.Teenistuskäik Tartu Ülikooli Molekulaarse ja Üldise Patoloogia Instituudi teadur 1991-1993. Lübeki Meditsiiniülikooli Inimesegeneetika Instituudi molekulaargeneetika grupi külalisteadlane 1993-1995. Hamburgi Ülikooli Inimesegeneetika Instituudi doktorant 1995-1998. Hamburgi Ülikooli Inimesegeneetika Instituudi teadur 1998-2002. Tallinna Tehnikaülikooli Geenitehnoloogia instituudi kutsutud professor 2002-2005. Tallinna Tehnikaülikooli Geenitehnoloogia instituudi dotsent 2005-
8.Teaduskraad Dr.rer.nat
9.Teaduskraadi välja
andnud asutus, aasta		 Hamburgi Ülikool, Bioloogiateaduskond, promoveeritud cum laude 1998.aastal
10.Tunnustused
11.Teadusorganisatsiooniline
ja –administratiivne
tegevus		 Eesti Inimesegeneetika Ühingu liige
12.Juhendamisel kaitstud
väitekirjad
13.Teadustöö põhisuunad Närvisüsteemi arengu ja funktsioonide molekulaarsed alused
14.Jooksvad grandid ETF grant 5915 (Retseptor pleksiin-B3 aktivatsioonirajad närvisüsteemi arengus, patoloogiates ja funktsioonis)
15.Teaduspublikatsioonid

Hartwig, C., Veske, A., Krejcova, S., Rosenbergerand, G., and Finckh, U. (2005) Plexin B3 promotes neurite outgrowth, interacts homophilically, and interacts with Rin. BMC Neurosci. 6(1): 53 (http://www.biomedcentral.com/1471-2202/6/53

Michelson P, Hartwig C, Schachner M, Gal A, Veske A, Finckh U. (2002) Missense mutations in the extracellular domain of the human neural cell adhesion molecule L1 reduce neurite outgrowth of murine cerebellar neurons. Hum Mutat. 20, pp. 481-6

Finckh, U., Schroder, J., Ressler, B., Veske, A., Gal, A. (2000) Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease. Am. J. Med. Genet. 92, pp. 40-46.

viimati muudetud: 30.09.2005

Curriculum Vitae (CV)
1.First Name Andres
2.Surname Veske
3.Institution Tallinn University of Technology, Departement of Gene Technology, Chair of Molecular Biology
4.Position assistant profesor
5.Date of birth 04.07.1965 (day.month.year)
6.Education Tallinn Secondary School No 43., graduated in 1983, University of Tartu, Faculty of Biology and Geography, graduated as cell biologist in 1991
7.Research and
professional experience		 Research assistant at the University of Tartu, Institute of Molecular and General Pathology, Chair of Human Biology and Genetics 1991-1993. Visiting scientists at the Medical University of Lübeck, Institute of Human Genetics, group of molecular genetics 1993-1995. Ph.D. student at the University of Hamburg, Institute of Human Genetics 1995-1998. Postdoctoral fellowship at the University of Hamburg, Institute of Human Genetics 1998-2002. Tallinn University of Technology, Departement of Gene technology, invited professor 2002-2005. Tallinn University of Technology, Departement of Gene technology, assistant professor 2005-
8.Academic degree Dr.rer.nat
9.Dates and sites of
earning the degrees		 University of Hamburg, Faculty of Biology, promotion cum laude in 1998
10.Honours/awards
11.Research-administrative
experience		 Member of the Estonian Society of Human Genetics
12.Supervised dissertations
13.Current research program Molecular biology of the CNS development and function
14.Current grant funding Grant from ESF 5915 (Receptor plexin-B3 activation pathways in the development, pathology and function of the nervous system)
15.List of most important publications

Hartwig, C., Veske, A., Krejcova, S., Rosenbergerand, G., and Finckh, U. (2005) Plexin B3 promotes neurite outgrowth, interacts homophilically, and interacts with Rin. BMC Neurosci. 6(1): 53 (http://www.biomedcentral.com/1471-2202/6/53

Michelson P, Hartwig C, Schachner M, Gal A, Veske A, Finckh U. (2002) Missense mutations in the extracellular domain of the human neural cell adhesion molecule L1 reduce neurite outgrowth of murine cerebellar neurons. Hum Mutat. 20, pp. 481-6

Finckh, U., Schroder, J., Ressler, B., Veske, A., Gal, A. (2000) Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease. Am. J. Med. Genet. 92, pp. 40-46.

last updated: 30.09.2005

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