Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Dimovski A"'
Autor:
Dzekova-Vidimliski P, Eftimovska-Otovikj N, Nikolov I G, Selim Gj, Rambabova-Bushljetik I, Pushevski V, Karanfilovski V, Matevska-Geshovska N, Dimovski A
Publikováno v:
Balkan Journal of Medical Genetics, Vol 26, Iss 2, Pp 27-34 (2024)
The polymorphism of the angiotensin-converting enzyme (ACE) gene and interleukin-1 beta (IL-1b) gene could be associated with resistance in the treatment of anemia in dialysis patients with recombinant human erythropoietin (rHuEPO). The aim of the st
Externí odkaz:
https://doaj.org/article/aab6c2e7dda24fa78d69f54610ed5873
Publikováno v:
Balkan Journal of Medical Genetics, Vol 26, Iss 2, Pp 35-40 (2024)
Clopidogrel, is a standard treatment in the prevention of major adverse cardiovascular events (MACE) in patients with coronary artery disease (CAD). Clopidogrel response is highly variable, mainly due to the presence of polymorphisms in the genes inv
Externí odkaz:
https://doaj.org/article/da5b9cbc1fc540559f18a73a83586699
Autor:
Popova-Labachevska M, Panovska-Stavridis I, Eftimov A, Kapedanovska Nestorovska A, Cevreska L, Ivanovski M, Ridova N, Trajkova S, Dimovski AJ
Publikováno v:
Balkan Journal of Medical Genetics, Vol 22, Iss 2, Pp 31-36 (2019)
The identification of the JAK2V617F mutation in several distinct myeloproliferative neoplasms (MPNs) raised the question how one single mutation incites expression of at least three different clinical phenotypes, i.e., polycythemia vera (PV), essenti
Externí odkaz:
https://doaj.org/article/2c38d23238de4936b1da294fbf181777
Autor:
Staninova-Stojovska M, Matevska-Geskovska N, Panovski M, Angelovska B, Mitrevski N, Ristevski M, Jovanovic R, Dimovski AJ
Publikováno v:
Balkan Journal of Medical Genetics, Vol 22, Iss 2, Pp 5-16 (2019)
Hereditary factors are assumed to play a role in ~35.0-45.0% of all colorectal cancers (CRCs) with about 5.0-10.0% associated with high penetrant disease-causing mutations in genes correlated to hereditary polyposis (HP) or hereditary non polyposis s
Externí odkaz:
https://doaj.org/article/ed75dbeefda447baaeecd21f23dbd0f0
Publikováno v:
Balkan Journal of Medical Genetics, Vol 19, Iss 1, Pp 91-94 (2016)
Nijmegen breakage syndrome (NBS) is a rare autosomal recessive chromosomal instability disorder characterized by microcephaly, immunodeficiency, radiosensitivity and a very high predisposition to malignancy. The gene responsible for the disease, NBS1
Externí odkaz:
https://doaj.org/article/71288b85b5854febb1ec0355cf71e2b4
Autor:
Daka Grapci A., Dimovski A. J., Kapedanovska A., Vavlukis M., Eftimov A., Matevska Geshkovska N., Labachevski N., Jakjovski K., Gorani D., Kedev S., Mladenovska Kristina
Publikováno v:
Balkan Journal of Medical Genetics, Vol 18, Iss 1, Pp 5-22 (2015)
As a membrane influx transporter, organic anion- transporting polypeptide 1B1 (OATP1B1) regulates the cellular uptake of a number of endogenous compounds and drugs. The aim of this study was to characterize the diversity of the solute carrier organic
Externí odkaz:
https://doaj.org/article/cb61f55a2b7e41bcb6f454df4ab29571
Autor:
Nestorovska Kapedanovska A., Jakovski K., Naumovska Z., Bajro Hiljadnikova M., Sterjev Z., Eftimov A., Geskovska Matevska N., Suturkova L., Dimitrovski K., Labacevski N., Dimovski A. J.
Publikováno v:
Balkan Journal of Medical Genetics, Vol 17, Iss 2, Pp 5-14 (2014)
Genetic variation in the regulation, expression and activity of genes coding for Phase I, Phase II drug metabolizing enzymes (DMEs) and drug targets, can be defining factors for the variability in both the effectiveness and occurrence of drug therapy
Externí odkaz:
https://doaj.org/article/633d2bff21fb41b298cc9b4a3b8de63f
Autor:
Sterjev Z, Kiteva G, Cvetkovska E, Petrov I, Kuzmanovski I, Ribarska T, Nestorovska K, Matevska N, Trajkovik-Jolevska S, Dimovski A, Suturkova Lj
Publikováno v:
Balkan Journal of Medical Genetics, Vol 15, Iss 1, Pp 19-24 (2012)
Externí odkaz:
https://doaj.org/article/319e3abda4e143929bbbca357a66635d
Publikováno v:
Balkan Journal of Medical Genetics, Vol 15, Iss 1, Pp 31-36 (2012)
Externí odkaz:
https://doaj.org/article/538819f95a664db2ad55ab0aa4318b5c
Autor:
Matevska N, Josifovski T, Kapedanovska A, Sterjev Z, Serafimoska Z, Panovski M, Jankulovski N, Petrusevska N, Angelovska B, Petrusevska G, Suturkova L, Dimovski A
Publikováno v:
Balkan Journal of Medical Genetics, Vol 11, Iss 2, Pp 17-24 (2008)
Externí odkaz:
https://doaj.org/article/a83e408a92a44bb3890b1bb1d32fd5f1