Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Momcilo, Ristanovic"'
Autor:
P Noveski, Momcilo Ristanovic, Marija Terzic, Dijana Plaseska-Karanfilska, Aleš Maver, Tanja Kunej, Alenka Hodžić, Branko Zorn, Borut Peterlin
Publikováno v:
Andrology. 9:212-220
STUDY QUESTION Are de novo mutations in the human genome associated with male infertility? SUMMARY ANSWER We identified de novo mutations in five candidate genes: SEMA5A, NEURL4, BRD2, CD1D, and CD63. WHAT IS KNOWN ALREADY Epidemiological and genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5c054dbad58e537b9086725d07d112c
https://doi.org/10.1111/andr.12897
https://doi.org/10.1111/andr.12897
Autor:
Jelena, Petrovic-Sunderic, Sandra, Dragicevic, Mina, Krnjajic, Momcilo, Ristanovic, Aleksandra, Nikolic, Zoran, Krivokapic
Publikováno v:
Journal of B.U.ON. : official journal of the Balkan Union of Oncology. 23(4)
The RAD51 gene plays an important role in homologous strand exchange in DNA repair. Two common single nucleotide polymorphisms in this gene, 135GC and 172GT, were associated with altered gene transcription. While 135GC was already linked to breast an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::08866b2f4b1aad0b2dba20a9a2001590
https://pubmed.ncbi.nlm.nih.gov/30358196
https://pubmed.ncbi.nlm.nih.gov/30358196
Autor:
Jovanka, Trifunovic, Mirjana, Prvanovic, Aleksandar, Jovanovic, Zoran, Dzamic, Miodrag, Lazic, Momcilo, Ristanovic, Sanja, Radojevic-Skodric, Gordana, Basta-Jovanovic
Publikováno v:
Journal of B.U.ON. : official journal of the Balkan Union of Oncology. 23(4)
The purpose of this study was to investigate into the expression of cyclin A and telomerase in renal cell carcinoma (RCC) and to analyze the relationship between expression and the clinicopathological characteristics of the tumor and their impact on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::092e167d759775a28d0823acf5a58994
https://pubmed.ncbi.nlm.nih.gov/30358218
https://pubmed.ncbi.nlm.nih.gov/30358218
Autor:
Aleksandra Božović, Nataša Tul, Keli Hočevar, Momcilo Ristanovic, Borut Peterlin, Ana Peterlin, Ana Mitrović Jovanović
Publikováno v:
European journal of obstetrics, gynecology, and reproductive biology. 231
Background Preterm birth is the largest contributor to newborn mortality, morbidity, and hospitalization in the first year of life worldwide. Previous studies have suggested the importance of genetic variation in the angiotensin-converting enzyme gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4d6ec5b628f18ba0a3c00a11be5f3ff
https://pubmed.ncbi.nlm.nih.gov/30366344
https://pubmed.ncbi.nlm.nih.gov/30366344
Autor:
Momcilo Ristanovic, Aleksandra Divac Rankov, Dragica Radojkovic, Aleksandra Nikolic, Ivan Paunovic, Vladan Zivaljevic
Publikováno v:
Experimental and Molecular Pathology. 99:100-103
As a key component of the transforming growth factor beta (TGFB) pathway, which regulates the expression of thyroid-specific genes, tumor suppressor SMAD4 is crucial for thyroid development and function. Aberrant expression of SMAD4 in thyroid tumor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75351d6f836a216afe23ed516082f511
https://doi.org/10.1016/j.yexmp.2015.06.005
https://doi.org/10.1016/j.yexmp.2015.06.005
Autor:
Srbislav Knezevic, Jovanka Trifunovic, Aleksandra Nikolic, Momcilo Ristanovic, Dragica Radojkovic, Filip Opincal
Publikováno v:
Archive of Oncology, Vol 23, Iss 2, Pp 17-19 (2017)
Archive of Oncology (2017) 23(2):17-19
Archive of Oncology (2017) 23(2):17-19
Background. Promoter hypermethylation of the SMAD4 gene has been registered in some cancer types, but in general doesn?t appear to be a frequent event in carcinogenesis. However, only a few published studies deal with this topic and not many cancer t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9f1eddf07487bf0aed338f1b7307fa3
https://scindeks-clanci.ceon.rs/data/pdf/0354-7310/2017/0354-73101702017N.pdf
https://scindeks-clanci.ceon.rs/data/pdf/0354-7310/2017/0354-73101702017N.pdf
Autor:
Polona Lavtar, Alenka Hodžić, Momcilo Ristanovic, Borut Peterlin, Jelena Dotlic, Ivana Novakovic
Publikováno v:
PLoS ONE, Vol 13, Iss 5, p e0196345 (2018)
PLoS ONE
PLoS ONE
Physiological studies in animals and human support an important role of circadian system in reproduction. The aim of this study was to investigate the potential association of CLOCK gene polymorphisms with idiopathic recurrent spontaneous abortion (I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09dd3626d3fd2b823b56ce038bbd1793
http://europepmc.org/articles/PMC5955485?pdf=render
http://europepmc.org/articles/PMC5955485?pdf=render
Autor:
Aleksandra, Nikolic, Marina, Vlajnic, Momcilo, Ristanovic, Jelena, Petrovic, Ivan, Dimitrijevic, Zoran, Krivokapic, Dragica, Radojkovic
Publikováno v:
Journal of B.U.ON. : official journal of the Balkan Union of Oncology. 22(1)
To analyze if cell-free (cf)DNA levels and the presence of KRAS and BRAF mutations in serum could be used as diagnostic biomarkers in patients with primary colorectal cancer (CRC).This study included 92 individuals who were operated due to primary CR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::34c846d46413bd0c7b13c7971e2eb0a1
https://pubmed.ncbi.nlm.nih.gov/28365952
https://pubmed.ncbi.nlm.nih.gov/28365952
Autor:
Andrija Bogdanovic, Vera Bunjevacki, Momcilo Ristanovic, Ljiljana Lukovic, Nela Maksimovic, Ivana Novakovic, Suzana Cvjeticanin, Biljana Jekic, Tatjana Damnjanovic
Publikováno v:
Archives of Biological Sciences, Vol 66, Iss 3, Pp 1055-1059 (2014)
Myelodysplastic syndromes (MDS) are clonal hematologic stem cell disorders with an as yet unknown molecular pathology. Genetic instability has been proposed as a cause of MDS. Mutations in the NBS1 gene, whose product nibrin (p95) is involved in DNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34b194697f3f1e0e72279fb512a2dec5
http://www.doiserbia.nb.rs/img/doi/0354-4664/2014/0354-46641403055B.pdf
http://www.doiserbia.nb.rs/img/doi/0354-4664/2014/0354-46641403055B.pdf
Autor:
Alenka Hodžić, Ivana Novakovic, Branko Zorn, Dijana Plaseska-Karanfilska, Aleš Maver, Cane Tulic, Borut Peterlin, Momcilo Ristanovic
Publikováno v:
Andrology. 5(1)
Summary The aim of this study was to examine whether there is an association among genetic variability in leptin (LEP) and leptin receptor (LEPR) genes and male infertility. We performed a case–control study and were searching for an association be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13b8de3969cb4a821917435e88c758e8
https://pubmed.ncbi.nlm.nih.gov/27813378
https://pubmed.ncbi.nlm.nih.gov/27813378