Search Results - "Hrasćan, Reno"
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1
Genetic and protein changes of E-cadherin in meningiomas
Published in Journal of cancer research and clinical oncology (01-05-2010)“…Purpose The molecular mechanisms and candidate genes involved in development of meningiomas still needs investigation and elucidation. Methods In the present…”
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2
Glioma Stem Cells-Features for New Therapy Design
Published in Cancers (19-04-2024)“…On a molecular level, glioma is very diverse and presents a whole spectrum of specific genetic and epigenetic alterations. The tumors are unfortunately…”
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3
Frequency of loss of heterozygosity of the NF2 gene in schwannomas from Croatian patients
Published in Croatian medical journal (01-08-2012)“…To identify gross deletions in the NF2 gene in a panel of schwannomas from Croatian patients in order to establish their frequencies in Croatian population…”
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4
Loss of heterozygosity of selected tumor suppressor genes in human testicular germ cell tumors
Published in Pathology, research and practice (15-03-2010)“…Human testicular germ cell tumors (TGCTs) are histologically heterogenous neoplasms with a variable malignant potential. Two main groups of germ cell tumors…”
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5
AXIN-1 protein expression and localization in glioblastoma
Published in Collegium antropologicum (01-01-2011)“…The etiology and pathogenesis of tumors of the central nervous system are still inadequately explained. In the present study the expression patterns of a…”
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6
Cuticle-associated bacteria can inhibit crayfish pathogen Aphanomyces astaci: Opening the perspective of biocontrol in astaciculture
Published in Aquaculture (25-02-2021)“…Pathogenic oomycete Aphanomyces astaci, the causative agent of crayfish plague, is listed among the world's 100 worst invasive alien species due to its fast…”
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Non-destructive method for detecting Aphanomyces astaci, the causative agent of crayfish plague, on the individual level
Published in Journal of invertebrate pathology (01-01-2020)“…[Display omitted] •We have developed a novel non-destructive Aphanomyces astaci-detection protocol.•The method detects A. astaci DNA in cuticle-associated…”
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8
Genetic changes of MLH1 and MSH2 genes could explain constant findings on microsatellite instability in intracranial meningioma
Published in Tumor biology (01-07-2017)“…Postreplicative mismatch repair safeguards the stability of our genome. The defects in its functioning will give rise to microsatellite instability. In this…”
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9
Nucleotide variations of TP53 exon 4 found in intracranial meningioma and in silico prediction of their significance
Published in Molecular and clinical oncology (01-12-2019)“…The aim of the present study was to identify TP53 exon 4 mutations in patients with meningioma and to investigate their potential association with specific…”
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10
AXIN1 Expression and Localization in Meningiomas and Association to Changes of APC and E-cadherin
Published in Anticancer research (01-09-2016)“…Tumor suppressor gene AXIN1 is an inhibitor of Wnt signaling pathway. It down-regulates the pathway's main signaling effector molecule, beta-catenin, in an…”
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11
Loss of p53 expression is accompanied by upregulation of beta‐catenin in meningiomas: a concomitant reciprocal expression
Published in International journal of experimental pathology (01-04-2016)“…Summary Crosstalk between Wnt and p53 signalling pathways in cancer has long been suggested. Therefore in this study we have investigated the involvement of…”
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12
Infrequent alteration of the DPC4 tumor suppressor gene in renal cell carcinoma
Published in Urolithiasis (01-06-2004)“…The aim of this study was to investigate the alterations in the DPC4 tumor suppressor gene in renal cell carcinoma (RCC). The study included 32 tumor specimens…”
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13
Histological groups of human postpubertal testicular germ cell tumours harbour different genetic alterations
Published in Anticancer research (01-08-2014)“…Testicular germ cell tumours are the most common malignancies in young males. Molecular biology studies of these tumours are often contradictory. Two…”
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14
Replication Error-positive Samples Found in Pheochromocytomas
Published in In vivo (Athens) (01-03-2005)“…Background: Adenomatous polyposis coli, (APC) and E-cadherin (CDH1) tumor suppressor genes were investigated in human pheochromocytoma. Both genes are…”
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15
Loss of heterozygosity of thenm23-H1 gene in human renal cell carcinomas
Published in Journal of cancer research and clinical oncology (01-12-1997)“…This study evaluates the potential contribution of thenm23-H1 gene to malignant transformation in patients with renal cell carcinoma. Using specific…”
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16
Effect of 905 MHz microwave radiation on colony growth of the yeast Saccharomyces cerevisiae strains FF18733, FF1481 and D7
Published in Radiology and oncology (01-06-2010)“…The aim of this study was to evaluate the effect of weak radiofrequency microwave (RF/MW) radiation emitted by mobile phones on colony growth of the yeast…”
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17
Loss of heterozygosity of CDKN2A (p16INK4a) and RB1 tumor suppressor genes in testicular germ cell tumors
Published in Radiology and oncology (01-09-2010)“…Testicular germ cell tumors (TGCTs) are the most frequent malignances in young adult men. The two main histological forms, seminomas and nonseminomas, differ…”
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18
Multiple genetic alterations in malignant metastatic insulinomas
Published in The Journal of pathology (01-12-1995)“…Proto-oncogenes, growth factors/receptors, and tumour suppressor genes were analysed in malignant metastatic insulinomas. Normal pancreas showed only a…”
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19
Molecular genetics of malignant insulinoma
Published in Anticancer research (01-07-1996)“…Malignant insulinoma is an rare form of cancer with poor prognosis and a reported 5-year survival of 35%. Relatively little is known about the etiology of this…”
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20
Narrowing of the region of allelic loss in 21q11-21 in squamous non-small cell lung carcinoma and cloning of a novel ubiquitin-specific protease gene from the deleted segment
Published in Genes chromosomes & cancer (01-02-2000)“…We examined 42 fresh non‐small cell lung carcinomas for allelic loss using 4 microsatellite markers located in a 4.5 Mb region in 21q11‐21, a gene‐poor…”
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