Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Martin von Janta-Lipinski"'
Autor:
Eckart Matthes, Stefan Kurek, Renate Mentel, Martin von Janta-Lipinski, Lutz Gürtler, Ursula Wegner
Publikováno v:
Medical Microbiology and Immunology. 189:91-95
Adenovirus (Ad) infection results in significant morbidity and mortality in both immunocompetent and immunosuppressed hosts. There is currently no licensed chemotherapy effective in dealing with this virus infection. In this study the anti-adenoviral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::461a7afd1aaa691b22ab2de0e423b7c5
https://doi.org/10.1007/s004300000046
https://doi.org/10.1007/s004300000046
Publikováno v:
Rapid Communications in Mass Spectrometry. 12:1889-1894
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) was used to explore noncovalent interactions between different peptides and ribose nucleic acids (RNAs). One RNA was mixed together with two or more peptides or vice versa to co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::691266d80cf2609a3cf0dfbb093f4846
https://doi.org/10.1002/(sici)1097-0231(19981215)12:23<1889::aid-rcm411>3.0.co
https://doi.org/10.1002/(sici)1097-0231(19981215)12:23<1889::aid-rcm411>3.0.co
Publikováno v:
Bioorganic & Medicinal Chemistry. 6:701-706
The synthesis of enantiomerically pure carbocyclic adenosine derivatives which have been prepared based on the kinetic resolution of a trans -2-(hydroxymethyl)cyclopentanol derivative is described. Their corresponding triphosphates were evaluated as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa9b64b4021e63f2beb963cdd6769168
https://doi.org/10.1016/s0968-0896(98)00021-2
https://doi.org/10.1016/s0968-0896(98)00021-2
Publikováno v:
Antiviral Research. 34:113-119
Antiviral effects of nucleoside analogues against human adenoviruses (ADV) belonging to subgroup B (ADV3) and C (ADV2) were comparatively analysed using focus reduction assay on Fogh and Lund (FL) cells. 3′-Fluoro-2′-deoxythymidine (FTdR), 3′-f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::200e8a3e422bd29b6847b70e71b12b9a
https://doi.org/10.1016/s0166-3542(97)01029-2
https://doi.org/10.1016/s0166-3542(97)01029-2
Publikováno v:
Journal of Virological Methods. 59:99-104
A method for screening of antiviral compounds against adenoviruses was established. Test compounds were diluted and plated in chamber slides for tissue culture. Drug-treated, virus-infected cultures were stained with fluorescein isothiocyanate conjug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1db4989eba97e10c9509b36df7a1319f
https://doi.org/10.1016/0166-0934(96)02026-5
https://doi.org/10.1016/0166-0934(96)02026-5
Autor:
L. S. Victorova, Fritz Theil, Alexander A. Krayevsky, Natalia B. Dyatkina, Dniitry Semizarov, Martin von Janta-Lipinski
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 14:723-726
A method was developed for synthesis of the four stereoisomeric enantiomerically pure 5′-nor carbocyclic nucleosides 4b, ent-4b, 10 and ent-10 starting from the common enantiomerically pure allylic monoacetate 1. Nucleoside analogues were converted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92e2430daf6f2a5d04d0af068f0ba17e
https://doi.org/10.1080/15257779508012458
https://doi.org/10.1080/15257779508012458
Publikováno v:
Tetrahedron. 51:761-772
A flexible synthesis of the four stereoisomeric enantiomerically pure 5′-nor carbocyclic adenosine analogues 4b , ent - 4b , 5b and ent - 5b starting from the common enantio-merically pure allylic monoacetate 3 has been developed. Each of the nucle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d67fd82402660ecc8058186f2ca1657
https://doi.org/10.1016/0040-4020(94)00986-5
https://doi.org/10.1016/0040-4020(94)00986-5
Publikováno v:
Tetrahedron Letters. 35:1961-1964
A flexible synthesis of the four stereoisomeric enantiomerically pure 5′-nor carbocyclic nucleosides 2b, ent-2b, 3b, and ent-3b starting from the common enantiomerically pure allylic monoacetate 1 has been developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::534f5c876be98b2831c0515e6bc76346
https://doi.org/10.1016/s0040-4039(00)73022-x
https://doi.org/10.1016/s0040-4039(00)73022-x
Autor:
Yong Wu, Eckart Matthes, Martin von Janta-Lipinski, Eugen Uhlmann, Christine Lehmann, Marianne Stulich, Lora Dimitrova
Publikováno v:
Oligonucleotides. 15(4)
Suppression of telomerase activity in tumor cells has been considered as a new anticancer strategy. Here, we present chimeric oligonucleotides (chimeric ODNs) as a new type of telomerase inhibitor that contains differently modified oligomers to addre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5d6dcd89b24babd76837817f3d54574
https://pubmed.ncbi.nlm.nih.gov/16396620
https://pubmed.ncbi.nlm.nih.gov/16396620
Publikováno v:
GBM Annual Fall meeting Berlin/Potsdam 2005. 2005
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8643937658152157a66fe9c33f870f70
https://doi.org/10.1240/sav_gbm_2005_h_001230
https://doi.org/10.1240/sav_gbm_2005_h_001230