Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Toni Josifovski"'
Publikováno v:
Makedonsko Farmacevtski Bilten, Vol 58, Iss (1, 2), Pp 15-24 (2012)
The most frequent type of hereditary colorectal cancer, the one occurring in the setting of the Lynch syndrome (LS) is considered a phenotypic manifestation of a germline defect in the mismatch repair mechanism i.e. in the MLH1, MSH2, MSH6 or PMS2 g
Externí odkaz:
https://doaj.org/article/2cc4f38ef4b94712b9dae92c24da2209
Publikováno v:
Makedonsko Farmacevtski Bilten, Vol 58, Iss (1, 2), Pp 15-24 (2012)
The most frequent type of hereditary colorectal cancer, the one occurring in the setting of the Lynch syndrome (LS) is considered a phenotypic manifestation of a germline defect in the mismatch repair mechanism i.e. in the MLH1, MSH2, MSH6 or PMS2 ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96957839c6ccff52659afe72d76eabf4
Publikováno v:
Croatian Medical Journal
Volume 53
Issue 5
Volume 53
Issue 5
Lynch syndrome (LS), formerly known as hereditary non-polyposis colorectal cancer (HNPCC), is considered the most common form of hereditary colorectal cancer (1). It is an autosomal dominantly inherited predisposition to early development of colorect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c0d769bcff2df601a4c63bc0bfae233
http://europepmc.org/articles/PMC3490460
http://europepmc.org/articles/PMC3490460
Autor:
Z Serafimoska, Bistra Angelovska, Milco Panovski, Zoran Sterjev, A Kapedanovska, Aleksandar Dimovski, Toni Josifovski, Natalija Angelovska Petrusevska, Ljubica Suturkova, G Petrusevska, Nikola Jankulovski, Nadica Matevska
Publikováno v:
Balkan Journal of Medical Genetics, Vol 11, Iss 2, Pp 17-24 (2008)
Methylenetetrahydrofolate Reductase C677T Polymorphism and Risk of Colorectal Cancer in the Macedonian PopulationMethylenetetrahydrofolate reductase (MTHFR) regulates the flow of folate groups between DNA synthesis and DNA methylation. A common C677T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::737c964a0abebc8e20799eb03bf678d7
https://doaj.org/article/a83e408a92a44bb3890b1bb1d32fd5f1
https://doaj.org/article/a83e408a92a44bb3890b1bb1d32fd5f1
Autor:
Zoran Sterjev, Natalija Angelovska Petrusevska, Z Serafimoska, Ljubica Suturkova, Marija Hiljadnikova-Bajro, Toni Josifovski, A Kapedanovska, S Despotovska, Milco Panovski, Aleksandar Dimovski, Nadica Matevska
Publikováno v:
Balkan Journal of Medical Genetics, Vol 10, Iss 2, Pp 29-36 (2007)
Cyclin D1 G870A Variant is Associated with Increased Risk of Microsatellite Instability-Positive Colorectal Cancer in Young Male PatientsCyclin D1 (CCND1) is a cell cycle regulatory protein, which is often over expressed in human tumors and is associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76048a512fb1b907e0efb52191e0ed92
https://doaj.org/article/8ea0562ed8ab4628b876172ac96dfe66
https://doaj.org/article/8ea0562ed8ab4628b876172ac96dfe66
Autor:
Milco Panovski, Toni Josifovski, Nikola Jankulovski, Marija Hiljadnikova Bajro, Aleksandar Dimovski, Aleksandra Kapedanovska Nestorovska, Nadica Matevska, Natalija Angelovska Petrusevska
Publikováno v:
Cancer genetics. 205(4)
Uridine diphosphoglucuronate glucuronosyltransferase 1A1 (UGT1A1) is the key hepatic detoxification enzyme involved in the biotransformation of many carcinogens implicated in the development of colon, breast, and prostate cancers in humans. A polymor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e81df447efcc7d3275053637b7e2e70c
https://pubmed.ncbi.nlm.nih.gov/22559977
https://pubmed.ncbi.nlm.nih.gov/22559977
Autor:
Biljana Angelovska, Nikola Mitrevski, Aleksandra Kapedanovska Nestorovska, Nadica Matevska, Aleksandar Dimovski, Djingis Jashar, Natalija Angelovska Petrusevska, Toni Josifovski, Aleksandar Eftimov
Publikováno v:
Annals of Oncology. 23:iv106
Introduction There is a significant variation in survival among patients with colon cancer treated with 5-FU-based therapies. Microsatellite instability (MSI) and 18q loss of heterozygosity (18qLOH) are most frequently associated with lack of benefit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b1e10556448dcbb84b8230b9cbce15b
https://doi.org/10.1016/s0923-7534(20)30195-2
https://doi.org/10.1016/s0923-7534(20)30195-2
Publikováno v:
Cancer Genetics and Cytogenetics. 203:83
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ac2c040261dedd99fd3a014ae7ee9fa
https://doi.org/10.1016/j.cancergencyto.2010.07.083
https://doi.org/10.1016/j.cancergencyto.2010.07.083
Autor:
N. Angelovska-Petrusevska, Aleksandar Eftimov, Toni Josifovski, A. Kapedanovska Nestorovska, Nadica Matevska, B. Angelovska-Grozdanovska, Aleksandar Dimovski
Publikováno v:
Journal of Clinical Oncology. 28:e14070-e14070
e14070 Background: There is a significant difference in survival and toxicity profiles among patients treated with 5-FU-based therapies. We evaluated the predictive value of TS promoter, MTHFR C677...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05050d9bdc32b9aa869a71e02d855f6d
https://doi.org/10.1200/jco.2010.28.15_suppl.e14070
https://doi.org/10.1200/jco.2010.28.15_suppl.e14070