SVIBOR - Papers - project code: 1-08-195

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Published papers on project 1-08-195


Quoted papers: 17
Other papers: 23
Total: 40


  1. Type of paper: Paper in journal

    Title: The fine structure of pepper chromoplasts: the effect of bleaching herbicides

    Authors:
    Salopek, Branka
    Ljubešić, Nikola
    Journal: Acta Botanica Croatica
    ISSN: 0365-0588
    Volume: 53
    Year: 1994
    Pages: from 7 to 13
    Number of references: 26
    Language: engleski
    Summary: The fine structure of plastids and the carotenoid content of ripening pepper fruits were studied. Red ripe fruits contained spindle-shaped chromoplasts which originated from leuco-chloroplasts. The bleaching herbicides amitrole and SAN 9789 inhibited the biosynthesis of total carotenoids and the development of typical spindle-shaped chromoplasts. Both herbicides prevented the formation of tubules and increased the accumulation of plastoglobules.
    Keywords: Capsicum annuum, chromoplast, herbicide, carotenoid biosynthesis, ultrastructure

  2. Type of paper: Paper in proceedings

    Title: Development of photosynthetic activity in plastids of greening roots

    Authors:
    Lukinić, Suzana
    Salopek, Branka
    Tomašević, Dijana
    Wrischer, Mercedes
    Editors
    Ljubešić, Nikola
    Proceedings title: Periodicum Biologorum, poseban broj: Proceedings of the 5th Congress of Croatian
    Language: engleski
    Place: Zagreb
    Year: 1994
    ISBN/ISSN: 00315362
    Pages: from 397 to 400
    Meeting: Peti kongres biologa Hrvatske
    Held: from 10/03/94 to 10/07/94
    Summary: The roots of some vascular plants become green when kept in the light. Chloroplasts first appeared in the oldest root zones, in the innermost parenchyma. The greening then gradually spread into more peripheral cell layers and into younger root segments. The number of photosynthetically active chloroplasts increased, during the greening process.
    Keywords: plastid in root, pigment, photosynthesis, ultrastructure

  3. Type of paper: Summary in proceedings

    Title:

    Authors:
    Kojić-Prodić, Biserka
    Nigović, Biljana
    Tomić, Sanja
    Ilić, Nebojša
    Magnus, Volker (82051)
    Giba, Zlatko
    Konjević, Radomir
    Proceedings title: Abstracts. 14th International Conference on Growth Substances
    Language: engleski
    Place: Amsterdam, Nizozemska
    Year: 1991
    Pages: from 68 to 68
    Meeting: Fourteenth International Conference on Plant Growth Substances
    Held: from 07/21/91 to 07/26/91
    Summary: The biological properties of the plant hormone (auxin)indol-3-ylacetic acid (IAA) and its ring-substituted derivativeshave so far been rationalized by hypotheses based on incompletestructural data. Here we compare the molecular structures of IAAand 5-(n-alkyl)indol-3-ylacetic acid (alkyl = methyl, ethyl,propyl, butyl), as revealed by X-ray crystallography andmolecular mechanics calculations, and their growth-promotingactivity in the Avena mesocotyl test. For the compounds studiedthe 5-(n-alkyl) residue was in an extended zig-zag conformationwith the C-alpha - C-beta bond perpendicular to, and the C-beta -C-gamma bond pointing away from the aromatic nucleus. In thecrystalline state, the methylene-carboxyl bond was perpendicularto the indole ring plane for 5-methylindole-3-ylacetic acid, andapproximately in that plane for the other IAA derivativesstudied. Crystal packing influences appear to be responsible forthis effect, as indicated by the results of molecular mechanicscalculations. In the potential energy-minimized conformation forthe isolated molecules in the gas phase, perpendicularorientation for the carboxyl group was always predominant. Theplant growth-promoting properties of the compounds studied werenot dramatically different. This indicates that a 5-substituentas bulky as n-butyl, in the orientation detailed above, does notsterically obstruct interaction with the auxin-binding protein(s)involved in the growth response.
    Keywords: Plant growth regulation, auxin, structure-activity relationships, X-ray crystallography, molecular mechanics, Avena sativa, mesocotyl test, indole-3-acetic acid, 5-methylindole-3-acetic acid, 5-ethylindole-3-acetic acid, 5-n-propylindole-3-acetic acid, 5-n-butylindole-3-acetic acid

  4. Type of paper: Summary in proceedings

    Title:

    Authors:
    Nigović, Biljana
    Kojić-Prodić, Biserka
    Tomić, Sanja
    Ilić, Nebojša
    Magnus, Volker (82051)
    Proceedings title: Collected Abstracts
    Language: engleski
    Year: 1991
    Pages: from 306 to 306
    Meeting: Thirteenth European Crystallographic Meeting
    Held: from 08/26/91 to 08/30/91

  5. Type of paper: Summary in proceedings

    Title:

    Authors:
    Namavari, Mohammed
    Laćan, Goran (58844)
    Satyamurthy, Nagichettiar
    Barrio, Jorge R.
    Editors
    Oteyza, Julian
    Proceedings title: Book of Abstracts
    Language: engleski
    Place: Washington, D.C., SAD
    Year: 1992
    ISBN/ISSN: 0-8412-2467-6
    Pages: from 0 to 0
    Meeting: 204th ACS National Meeting
    Held: from 08/23/92 to 08/28/92
    Summary: The importance of 6-(F-18)fluoro-L-DOPA (6-FDOPA) for probingthe central dopamine metabolism in vivo in humans using positronemission tomography (PET) has promoted considerable interest inits synthesis. We report a new method for the synthesis of6-FDOPA and other fluorinated analogs of L-DOPA based on aregioselective radiofluorodestannylation procedure usingelementary F-18 and (F-18) acetyl hypofluorite. We have preparedfor the first timeN-formyl-3,4-di-t-butoxycarbonyloxy-6-(trimethylstannyl)-L-phenylalanin e ethyl ester (1) as an ideal precursor of 6-FDOPA, whichefficiently and directly reacts with elementary F-18. Theregioselective radiofluorodestannylation of 1 with F-18 and(F-18) acetyl hypofluorite afforded, after acidic hydrolysis,6-FDOPA with a radiochemical yield of 25% (theoretical maximum:50%), ready for human use. Similarly, 6-(F-18) and 4-(F-18)fluoro-L-m-tyrosine (6-FMT and 4-FMT) were synthesized from thecorresponding 6- and 4-trimethylstannyl-L-m-tyrosine derivativesin 23 and 11% radiochemical yields, respectively. Likewise,4-(F-18)fluoro-beta-fluoromethylene-m-tyrosine (4-FMFMT), aprobe for monoamine oxidase in dopaminergic terminals, wassynthesized from the corresponding 4-trimethylstannylbeta-fluoromethylene m-tyrosine derivative in 7% radiochemicalyield. The procedure can also be extended to the synthesis offluoromethyl-4-(or 6-) (F-18)fluoroarylalanine derivatives thatmay be used as probes for aromatic amino acid decarboxylase basedon suicide enzyme inhibition mechanisms.
    Keywords: Human brain, in vivo positron emission tomography, dopamine metabolism, F-18 labeling, trimethylstannyl derivatives, acetyl hypofluorite, 6-fuoro-L-DOPA, 6-fuoro-L-m-tyrosine, 4-fluoro-L-m-tyrosine, 4-fluoro-beta-fluoromethylene-m-tyrosine, 6-(F-18)fluoro-L-DOPA, 6-(F-18)fluoro-L-m-tyrosine, 4-(F-18)fluoro-L-m-tyrosine, 4-(F-18)fluoro-beta-fluoromethylene-m-tyrosine, aromatic amino acid decarboxylase.

  6. Type of paper: Summary in proceedings

    Title: Radiofluorinated enzyme probes of dopaminergic function

    Authors:
    Barrio, Jorge R.
    Satyamurthy, Nagichettiar
    Namavari, Mohammed
    Laćan, Goran (58844)
    Proceedings title: Abstracts of Papers
    Language: engleski
    Place: Chicago, SAD
    Year: 1993
    ISBN/ISSN: 0-8412-2620-2
    Pages: from 0 to 0
    Meeting: 206th ACS National Meeting,
    Held: from 08/22/93 to 08/27/93
    Summary: 6-(F-18)-Fluoro-L-DOPA (FDOPA), a functional analog of exogenousL-DOPA is useful to determine in-vivo aromatic amino aciddecarboxylase (AAAD) mediated decarboxylation and apparentdopamine turnover rates. Also, 4- (4-FMT) and6-(F-18)fluoro-L-m-tyrosines (6-FMT) are analogs that essentiallyfollow the L-DOPA pathway of central metabolism, without3-O-methylation or extensive peripheral metabolism.Interestingly, molecular and enzymatic mechanisms involved intheir retention in central brain structures differ substantially.In addition, radiofluorinated enzyme probes based on theprinciple of dual-enzyme (AAAD-MAO) inhibition will be discussedwith respect to the influence of stereo- and geometric isomerismson the enzymatic behavior and central kinetics in primates.Finally, analogs that bind selectively and covalently to AAAD(e.g. alpha-fluoromethyl-6-(F-18)fluoro-L-DOPA) will beintroduced. All these analogs will be presented in a context of auseful strategy for designing radiotracers to probe specificenzymes and their functions.
    Keywords: Central nervous system, primates, L-DOPA decarboxylation, dopamine turnover, F-18 labeling, radiofluorinated enzyme probes, aromatic amino acid decarboxylase (AAAD), monoamine oxidase (MAO), 6-fluoro-L-DOPA, 4-fluoro-L-m-tyrosine, 6-fluoro-L-m-tyrosine, alpha-fluoromethyl-6-fluoro-L-DOPA, 6-(F-18)fluoro-L-DOPA, 4-(F-18)fluoro-L-m-tyrosine, 6-(F-18)fluoro-L-m-tyrosine, alpha-fluoromethyl-6-(F-18)fluoro-L-DOPA.

  7. Type of paper: Summary in proceedings

    Title: L-(E)-beta-fluoromethylene-6-(F-18)fluoro-m-tyrosine: a specific central dopamine probe

    Authors:
    Barrio, Jorge R.
    Laćan, Goran (58844)
    Satyamurthy, Nagichettiar
    Yu Chu, Dan
    Cheng Huang, Sung
    Phelbs, Michael E.
    Editors
    Strauss, William H.
    Proceedings title: Journal of Nuclear Medicine. JNM
    Language: engleski
    Place: New York, USA
    Year: 1993
    ISBN/ISSN: 0161-5505
    Pages: from 202 to 202
    Meeting: Proceedings of the 40th Annual Meeting of the Society of Nuclear Medicine, Inc.,
    Held: from 06/08/93 to 06/11/93
    Summary: We have investigated the stereo (D,L) and geometric (E,Z)specificity of radiofluorinated beta-fluoromethylene-m-tyrosine(FMFMT) derivatives as probes for the central dopaminergic systemwith positron emission tomography. The individual6-radiofluorinated enantiomers: L- E , D- E , and the D,L- Z andD,L- E isomers were prepared by direct radiofluorination, with(F-18)acetylhypofluorite, of the corresponding precursors andpurified by preparative C-18 reverse phase HPLC. Macacanemestrina monkeys (with carbidopa (CD), 5 mg/kg; n = 6 andwithout CD; n= 2) were injected IV with the purifiedradiofluorinated isomers (see above) (5 - 12 mCi) and thedistribution of activity followed in central brain structures.The L- E FMFMT isomer was the only one showing specific striatallocalization of activity (striatum:cerebellum ratio: 3.00+-0.43(w/CD); 4.25+-0.35 (wo/CD) at 2h). FMFMT tissue-time activitydata (Patlak) showed essentially irreversible metabolic trappingof the activity in dopaminergic structures: L- E FMFMT:Distribution volume (Dv) = 1,0; K3 = 0.0067 +-0.0018 (n = 4);D,L- E FMFMT; Dv = 0.5; 0.0034+-0.0008 (n=2). Neither the D- Estereomer nor the L- Z (or D- Z ) geometric isomers showed anysignifficant in vivo striatal localization probably due to theirrestricted BBB permeability. L E FMFMT arterial plasmametabolites also have poor BBB permeability. The striatalbehavior of L- E FMFMT is consistent with its aromatic amino aciddecarboxylase mediated decarboxylation. This combined with itslow peripheral metabolism (10% metabolites w/CD and 20% wo/CD upto 2h) makes it a valuable PET tracer for assessment of centraldopaminergic mechanisms.
    Keywords: Central nervous system, corpus striatum, cerebellum, dopaminergic structures, brain blood barrier, peripheral metabolism, positron emission tomography, radiofluorinated enzyme probes, F-18 labeling, Macaca nemestrina, monkey, E-beta-fluoromethylene-6-fluoro-L-m-tyrosine, E-beta-fluoromethylene-6-fluoro-D-m-tyrosine, E-beta-fluoromethylene-6-fluoro-DL-tyrosine, Z-beta-fluoromethylene-6-(F-18)fluoro-L-m-tyrosine, E-beta-fluoromethylene-6-(F-18)-fluoro-D-m-tyrosine, E-beta-fluoromethylene-6-(F-18)-fluoro-DL-m-tyrosine, Z-beta-fluoromethylene-6-(F-18)-fluoro-DL-m-tyrosine, aromatic amino acid decarboxylase.

  8. Type of paper: Summary in proceedings

    Title: Structure Activity Relationships of Auxins and its Derivatives

    Authors:
    Kojić-Prodić, Biserka
    Nigović, Biljana
    Tomić, Sanja
    Horvatić, Davor
    Magnus, Volker (82051)
    Proceedings title: XII Sastanak kemičara Hrvatske, Knjiga sažetaka
    Language: hrvatski
    Place: Zagreb
    Year: 1991
    Pages: from 30 to 30
    Meeting: XII Sastanak kemičara Hrvatske
    Held: from 02/11/91 to 02/13/91

  9. Type of paper: Summary in proceedings

    Title: Synthesis of Biologically Active Alkylindole-3-acetic Acids

    Authors:
    Ilić, Nebojša
    Iskrić, Sonja (17071)
    Kojić-Prodić, Biserka
    Magnus, Volker (82051)
    Nigović, Biljana
    Proceedings title: XII Sastanak kemičara Hrvatske, Kniga sažetaka
    Language: hrvatski
    Place: Zagreb
    Year: 1991
    Pages: from 147 to 147
    Meeting: XII Sastanak kemičara Hrvatske
    Held: from 02/11/91 to 02/13/91

  10. Type of paper: Summary in proceedings

    Title: Sinteza beta-D-glukozil estera karbonil-13C indol-3-octene kiseline

    Authors:
    Jakas, Andreja (192222)
    Magnus, Volker (82051)
    Horvat, Štefica (51440)
    Sandberg, Goran
    Proceedings title: XIII Skup Hrvatskih kemičara, Knjiga sažetaka
    Language: engleski
    Place: Zagreb
    Year: 1993
    Pages: from 154 to 154
    Meeting: XIII Skup Hrvatskih kemičara
    Held: from 02/08/93 to 02/10/93

  11. Type of paper: Summary in proceedings

    Title: Utjecaj halogeniranja biljnog hormona-auksina na biološku aktivnost

    Authors:
    Nigović, Biljana
    Kojić-Prodić, Biserka
    Puntarec, Vitomir
    Magnus, Volker (82051)
    Proceedings title: XIII Skup Hrvatskih kemičara, Knjiga sažetaka
    Language: engleski
    Place: Zagreb
    Year: 1993
    Pages: from 304 to 304
    Meeting: XIII Skup Hrvatskih kemičara
    Held: from 02/08/93 to 02/10/93

  12. Type of paper: Summary in proceedings

    Title: Effect of auxins on pea pericarp growth

    Authors:
    Reinecke, Dennis M.
    Ozga, Jocelyn A.
    Magnus, Volker (82051)
    Editors
    Ort, Donald R.
    Raskin, Ilya
    Green, P.
    Tuan-Hua Ho, David
    DuPont, Frances M.
    Randall, Douglas D.
    Siedow, James N.
    Proceedings title: Plant Physiology, Supplement toVolume 105, number 1
    Language: engleski
    Place: Rockville, Maryland, SAD
    Year: 1994
    ISBN/ISSN: 0032-0889
    Pages: from 139 to 139
    Meeting: 1994 Annual Meeting of the American Society of Plant Physiologists
    Held: from 07/30/94 to 08/03/94
    Summary: Pea (Pisum sativum L.) fruits contain the auxins indole-3-acetic acid (IAA) and 4-chloroindole-3-acetic acid (4-Cl-IAA). To understand the effect of the halogen on biological activity, IAA and its analogues substituted with chlorine or fluorine in ring positions 4, 5, 6, or 7 were applied to deseeded pea fruits. While 4-Cl-IAA sustained almost normal growth, the other halogenated compounds were less effective. With IAA, and in controls without auxin, the deseeded fruits did not grow and abscised.
    Keywords: Pisum sativum, pea, auxin, indole-3-acetic acid, 4-chloroindole-3-acetic acid, ring-halogenated indole-3-acetic acids, fruit development.
    Other: Sažetak nosi radni broj 761

  13. Type of paper: Summary in proceedings

    Title: 4-Cl-IAA, a potent substitute for seeds to promote pea pericarp growth

    Authors:
    Brenner, Mark L.
    Sheng, Chuxing
    Magnus, Volker (82051)
    Editors
    Zeevaart, Jan
    Goldsmith, Mary Helen
    Hangarter, Roger
    Proceedings title: Program - Abstracts (15thInternational Conference of Plant Growth Substances)
    Language: engleski
    Place: Minneapolis, Minnesota, SAD
    Year: 1995
    Pages: from 00 to 00
    Meeting: 15th International Conference on Plant Growth Substances
    Held: from 07/14/95 to 07/18/95
    Summary: Deseeding pea (Pisum sativum L.) fruits arrests the growth of the pericarp, followed by its abscission. Application of auxins or gibberellins partially reverses the effect of seed removal. 4-Cl-IAA, an endogenous auxin of peas, is uniquely active. One of its effects appears to be a stimulation of the oxidation of GA-19 to GA-20, a significant step in the biogenesis of bioactive gibberellins.
    Keywords: Pisum sativum, pea, fruit growth, auxin, gibblerellin, indole-3-acetic acid, 4-chloroindole-3-acetic acid, GA-19, GA-20
    Other: Sažetak nosiredni broj 048

  14. Type of paper: Summary in proceedings

    Title: Structure-activity correlatons for ring-fluorinated indole-3-acetic acids

    Authors:
    Antolić, Snježana
    Kojić-Prodić, Biserka
    Tomić, Sanja
    Magnus, Volker (82051)
    Cohen, Jerry D.
    Editors
    Zeevaart, Jan
    Goldsmith, Mary Helen
    Hangarter, Roger
    Proceedings title: Program - Abstracts (15th International Conference of Plant Growth Substances)
    Language: engleski
    Place: Minneapolis, Minnesota, SAD
    Year: 1995
    Pages: from 00 to 00
    Meeting: 15th International Conference on Plant Growth Substances
    Held: from 07/14/95 to 07/18/95
    Summary: As a part of molecular recognition studies on auxins, a series of indole-3-acetic acids (IAAs) fluorinated at ring-positions 4, 5, 6 or 7 was examined by X-ray crystallography and by molecular mechanics and dynamics simulations. No major conformational differences were detected. The growth-promoting properties of IAA and its fluorinated analogues in the Avena coleoptile straight-growth test were nearly the same, except for 4-F-IAA which was about 10 times more active.
    Keywords: indole-3-acetic acid, 4-fluoroindole-3-acetic acid, 5-fluoroindole-3-acetic acid, 6-fluoroindole-3-acetic acid, 7-fluoroindole-3-acetic acid, X-ray crystallography, molecular mechanics, molecular dynamics, auxin activity, Avena coleoptile straight growth test
    Other: sažetak nosi radni broj 246

  15. Type of paper: Summary in proceedings

    Title: Effect of bleaching herbicides SAN 9789 and amitrole on the structure ofpepper chromoplasts

    Authors:
    Salopek, Branka
    Ljubešić, Nikola
    Proceedings title: Zbornik sažetaka priopćenja 5. kongresa biologa Hrvatske
    Language: hrvatski
    Place: Zagreb
    Year: 1994
    Pages: from 197 to 198
    Meeting: Peti kongres biologa Hrvatske
    Held: from 10/03/94 to 10/07/94
    Summary: Plastid ultrastructure and carotenoid content of pepper (Capsicum annuum L.) fruits was studied, along with the changes caused by the herbicides SAN 9789 and amitrole. During ripening, the leuco-chloroplasts of the young fruit transformed into spidle-shaped chromoplasts filled with numerous tubules and plastoglobules. Simultaneously, the chlorophyll disappeared, and carotenoid levels increased. The two herbicides inhibited carotenoid synthesis and typical chromoplast development, but stimulated the formation of plastoglobules.
    Keywords: Capsicum annuum, fruit ripening, plastid development, chromoplast, ultrastructure, SAN 9789, amitrole, chlorophyll, carotenoid, plastoglobule
    Other: Engleski sažetak

  16. Type of paper: Summary in proceedings

    Title: Synthesis of stereo (R and S) and geometric (E and Z) (F-18)fluoro-beta-fluoromethylene-m-tyrosine derivatives: specific PET probles for central dopaminergic system

    Authors:
    Laćan, Goran (58844)
    Barrio, Jorge R.
    Satyamurthy, Nagichettiar
    Yu Chu, Dan
    Huang, Sung-Cheng
    Phelbs, Michael E.
    Editors
    Ivančević, D.
    Proceedings title: Book of Abstracts, First Croatian International Congress of Nuclear Medicine
    Language: engleski
    Place: Zagreb
    Year: 1994
    Pages: from 00 to 00
    Meeting: First Croatian International Congress of Nuclear Medicine
    Held: from 10/13/94 to 10/15/94
    Summary: Racemic beta-fluoromethylene-m-tyrosine (FMMT) is used as an aromatic amino acid decarboxylase-activated monoamine oxidase inhibitor. We separated the geometric and optical isomers and introduced F-18 at specific positions of the aromatic nucleus. In vivo striatal localization, as shown by positron emission tomography (PET), decreased in the order: 6F-S-(E)-FMMT > 2F-S(E)-FMMT > 4F-R,S-(E)-FMMT, and was undetetable for radiofluorinated analogs of R-(E)-FMMT and R,S-(Z)-FMMT.
    Keywords: beta'fluormethylene-m-tyrosine, monoamine oxidase, aromatic amino acid decarboxylase, inhibitor, F-18-labeling, positron emission tomography, corpus striatum, dopaminergic system
    Other: sažetak nosi redni broj V50

  17. Type of paper: Ph.D.

    Title: Structure-activity relationships for auxins, a class of plant growth hormones
    Faculty: Farmaceutsko-biokemijski fakultet Sveučilište u Zagrebu
    Date of defense: 10/29/92
    Language: hrvatski
    Number of pages: 89
    Keywords: Plant hormone, structure-activity relationships, molecular structure, crystal structure, x-ray structural analysis, molecular mechanics, molecular dynamics, conformational analysis, conformation of bioactive molecules, indole-3-acetic acid, n-alkylindole-3-acetic acid, haloindole-3-acetic acid.


  18. Type of paper: M.A.

    Title: Ultrastructural and biochemical studies on chloroplast differentiation in potato roots in vitro
    Faculty: Poslijediplomski studij prirodnih znanosti (Molekularna i stanična biologija) Sveučilište u Zagrebu
    Author: SALOPEK BRANKA
    Date of defense: 03/17/95
    Language: hrvatski
    Number of pages: 78
    Summary: Light-induced chloroplast differentiation was studied in cultures of adventitious roots formed in vitro and in hairy roots transformed with Agrobacterium rhizogenes, strain 8196. Hairy roots greened faster than normal cultured roots, and the chlorophyl content and the photosynthetic activity of their chloroplasts was higher than that of normal roots.
    Keywords: Solanum tuberosum, potato, Agrobacterium rhizogenes 8196, plastid, chloroplast, root, hairy root, pigment, chlorophyll, photosynthetic activity


  19. Type of paper: Mentorship

    Title: Structure-activity relationships for auxins, a class of plant growth hormones
    Faculty: Farmaceutsko-biokemijski fakultet Sveučilište u Zagrebu
    Date of defense: 10/29/92
    Number of pages: 89
    Author: Nigović Biljana
    Degree level: Ph.D.


  20. Type of paper: Mentorship

    Title: Ultrastructural and biochemical studies on chloroplast differentiation in potato roots in vitro
    Faculty: Poslijediplomski studij prirodnih znanosti (Molekularna i stanična biologija) Sveučilište u Zagrebu
    Mentor: MAGNUS VOLKER
    Date of defense: 03/17/95
    Number of pages: 78
    Author: Salopek magistar Branka
    Degree level: M.A.


  21. Type of paper: Invited lecture

    Title: Probing dopaminergic mechanisms with dual-enzyme
    Institution: Department of Molecular and Medical Pharmacology, UCLA School of Medicine
    Year: 1995


  22. Type of paper: Invited lecture

    Title: Fluorinated m-tyrosine derivates and PET imaging
    Institution: Zavod za organsku kemiju i biokemiju, Institut "Ruđer Bošković"
    Year: 1994


  23. Type of paper: Invited lecture

    Title: Auxi structure and function
    Institution: Department of Horticultural Science, University of Minnesota
    Year: 1994



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