Year |
Citation |
Score |
2020 |
Alzeer J, Abou Hadeed K, Basar H, Al-Razem F, Abdel-Wahhab MA, Alhamdan Y. Cannabis and Its Permissibility Status. Cannabis and Cannabinoid Research. PMID 33998850 DOI: 10.1089/can.2020.0017 |
0.208 |
|
2020 |
Alzeer J. Halal Certification of Food, Nutraceuticals, and Pharmaceuticals in the Arab World Springer, Cham. DOI: https://doi.org/10.1007/978-3-319-74365-3_36-1 |
0.196 |
|
2020 |
Alzeer J. Cannabis and Its Permissibility Status Cannabis and Cannabinoid Research. DOI: 10.1089/can.2020.0017 |
0.169 |
|
2020 |
Alzeer J. Good agricultural practices and its compatibility with Halal standards Trends in Food Science & Technology. DOI: 10.1016/J.Tifs.2020.02.025 |
0.342 |
|
2019 |
Alzeer J. Halalopathy: A science of trust in medicine. Journal of Integrative Medicine. PMID 30948352 DOI: 10.1016/J.Joim.2019.03.005 |
0.339 |
|
2019 |
Alzeer J. Halalopathy: A science of trust in medicine Journal of Integrative Medicine. 17: 150–154.. DOI: https://doi.org/10.1016/j.joim.2019.03.005 |
0.183 |
|
2018 |
Triemer T, Messikommer A, Glasauer SMK, Alzeer J, Paulisch MH, Luedtke NW. Superresolution imaging of individual replication forks reveals unexpected prodrug resistance mechanism. Proceedings of the National Academy of Sciences of the United States of America. PMID 29378947 DOI: 10.1073/Pnas.1714790115 |
0.664 |
|
2018 |
Alzeer J. Halalopathic: A New Concept in Medicine Alzeer, J Mol Genet Med. 12. DOI: 10.4172/1747-0862.1000353 |
0.226 |
|
2018 |
Alzeer J. Rational and practical aspects of Halal and Tayyib in the context of food safety Trends in Food Science & Technology. 71: 264-267. DOI: 10.1016/J.Tifs.2017.10.020 |
0.317 |
|
2017 |
Naik A, Alzeer J, Triemer T, Bujalska A, Luedtke NW. Chemoselective Modification of Vinyl DNA by Triazolinediones. Angewandte Chemie (International Ed. in English). PMID 28561928 DOI: 10.1002/Anie.201702554 |
0.698 |
|
2016 |
Alzeer J. Swiss Scientific Society for Developing Countries: A Concept of Relationship International Journal of Humanities and Social Sciences. 10. DOI: doi.org/10.5281/zenodo.1123801 |
0.194 |
|
2016 |
Alzeer J, Abou Hadeed K. Ethanol and its Halal status in food industries Trends in Food Science & Technology. 58: 14-20. DOI: 10.1016/J.Tifs.2016.10.018 |
0.316 |
|
2016 |
Seyfried MS, Alzeer J, Luedtke NW. Molecular Design and Synthesis of a Planar Telomestatin Analogue European Journal of Organic Chemistry. 2016: 367-372. DOI: 10.1002/Ejoc.201501103 |
0.625 |
|
2013 |
Vummidi BR, Noreen F, Alzeer J, Moelling K, Luedtke NW. Photodynamic agents with anti-metastatic activities. Acs Chemical Biology. 8: 1737-46. PMID 23672401 DOI: 10.1021/Cb400008T |
0.609 |
|
2013 |
Vummidi BR, Alzeer J, Luedtke NW. Fluorescent probes for G-quadruplex structures. Chembiochem : a European Journal of Chemical Biology. 14: 540-58. PMID 23440895 DOI: 10.1002/Cbic.201200612 |
0.666 |
|
2012 |
Hentschel S, Alzeer J, Angelov T, Schärer OD, Luedtke NW. Synthesis of DNA interstrand cross-links using a photocaged nucleobase. Angewandte Chemie (International Ed. in English). 51: 3466-9. PMID 22344895 DOI: 10.1002/Anie.201108018 |
0.731 |
|
2012 |
Hentschel S, Alzeer J, Angelov T, Schärer OD, Luedtke NW. Synthese von DNA-Interstrang-Crosslinks unter Verwendung einer photoaktivierbaren Nucleobase Angewandte Chemie. 124: 3523-3526. DOI: 10.1002/Ange.201108018 |
0.73 |
|
2010 |
Alzeer J, Luedtke NW. pH-mediated fluorescence and G-quadruplex binding of amido phthalocyanines. Biochemistry. 49: 4339-48. PMID 20380429 DOI: 10.1021/Bi9020583 |
0.674 |
|
2010 |
Membrino A, Paramasivam M, Cogoi S, Alzeer J, Luedtke NW, Xodo LE. Cellular uptake and binding of guanidine-modified phthalocyanines to KRAS/HRAS G-quadruplexes. Chemical Communications (Cambridge, England). 46: 625-7. PMID 20062883 DOI: 10.1039/B918964E |
0.662 |
|
2009 |
Alzeer J, Vummidi BR, Roth PJ, Luedtke NW. Guanidinium-modified phthalocyanines as high-affinity G-quadruplex fluorescent probes and transcriptional regulators. Angewandte Chemie (International Ed. in English). 48: 9362-5. PMID 19882707 DOI: 10.1002/Anie.200903685 |
0.684 |
|
2009 |
Alzeer J, Roth PJ, Luedtke NW. An efficient two-step synthesis of metal-free phthalocyanines using a Zn(ii) template. Chemical Communications (Cambridge, England). 1970-1. PMID 19333460 DOI: 10.1039/B822985F |
0.624 |
|
2009 |
Alzeer J, Vummidi B, Roth P, Luedtke N. Guanidinium-modifizierte Phthalocyanine als Fluoreszenzsonden mit hoher G-Quadruplex-Affinität und als Transkriptionsregulatoren Angewandte Chemie. 121: 9526-9529. DOI: 10.1002/Ange.200903685 |
0.329 |
|
2006 |
Alzeer J, Schärer OD. A modified thymine for the synthesis of site-specific thymine-guanine DNA interstrand crosslinks. Nucleic Acids Research. 34: 4458-66. PMID 16945959 DOI: 10.1093/Nar/Gkl587 |
0.67 |
|
2005 |
Gillet LC, Alzeer J, Schärer OD. Site-specific incorporation of N-(deoxyguanosin-8-yl)-2-acetylaminofluorene (dG-AAF) into oligonucleotides using modified 'ultra-mild' DNA synthesis. Nucleic Acids Research. 33: 1961-9. PMID 15814813 DOI: 10.1093/Nar/Gki335 |
0.696 |
|
2000 |
Alzeer J, Chollet J, Heinze-Krauss I, Hubschwerlen C, Matile H, Ridley RG. Phenyl beta-methoxyacrylates: a new antimalarial pharmacophore. Journal of Medicinal Chemistry. 43: 560-8. PMID 10691682 DOI: 10.1021/Jm990002Y |
0.38 |
|
1996 |
Alzeer J, Nock N, Wassner G, Masciadri R. MOM-protected 3-hydroxy-5-phenyl-isoxazole: Regioselective preparation and synthetic application Tetrahedron Letters. 37: 6857-6860. DOI: 10.1016/0040-4039(96)01547-X |
0.415 |
|
1995 |
Alzeer J, Vasella A. Oligosaccharide Analogues of Polysaccharides. Part 4. Synthesis of a monosaccharide-derived octamer Helvetica Chimica Acta. 78: 1219-1237. DOI: 10.1002/Hlca.19950780515 |
0.589 |
|
1995 |
Alzeer J, Cai C, Vasella A. Oligosaccharide Analogues of Polysaccharides. Part 1. Concept and synthesis of monosaccharide-derived monomers Helvetica Chimica Acta. 78: 242-264. DOI: 10.1002/Hlca.19950780122 |
0.681 |
|
1995 |
Alzeer J, Vasella A. Oligosaccharide Analogues of Polysaccharides. Part 2. Regioselective deprotection of monosaccharide-derived monomers and dimers Helvetica Chimica Acta. 78: 177-193. DOI: 10.1002/Hlca.19950780117 |
0.568 |
|
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