biomedicina slovenica

"Genes" : 3975

Ihrler Stephan; Stiefel David; Jurmeister Philipp; Sandison Ann; Chaston Nicola; Laco Jan; Zidar Nina; Brčić Luka; Stoehr Robert; Agaimy Abbas
Salivary carcinosarcoma
2022 ►
Glavač Damjan; Mladinić Miranda; Ban Jelena; Mazzone Graciela L.; Sámano Cynthia; Tomljanović Ivana; Jezernik Gregor; Ravnik-Glavač Metka
The potential connection between molecular changes and biomarkers related to ALS and the development and regeneration of CNS
2022 ►
Pavlič Alenka; Alaluusua Satu
Enamel microstructure of hypocalcified type of amelogenesis imperfecta (AL)
2008 ►
Urh Kristian; Zidar Nina; Boštjančič Emanuela
Bioinformatics analysis of RNA-seq data reveals genes related to cancer stem cells in colorectal cancerogenesis
2022 ►
Šajn Mihela; Luzar Boštjan; Zver Samo
Wells’ syndrome possibly caused by hematologic malignancy, influenza vaccination or ibrutinib
2022 ►
Oražem Miha; Draulans Cédric; Spaas Mathieu; Cutsem Eric Van; Debecker Marina; Meerleer Gert De; Tejpar Sabine; Dekervel Jeroen; Haustermans Karin
A fatal wound complication following sequential anti-angiogenesis, immune checkpoint inhibition and ultra-hypofractionated radiotherapy
2021 ►
Strojnik Ksenija; Krajc Mateja; Šetrajčič Dragoš Vita; Stegel Vida; Novaković Srdjan; Blatnik Ana
Genetic testing results in Slovenian male breast cancer cohort indicate the BRCA2 7806-2A > G founder variant could be associated with higher male breast cancer risk
2021 ►
Lemmers Richard J. L. F.; Vliet Patrick van der; Blatnik Ana; Balogh Judit; Zidar Janez; Henderson D.; Goselink Rianne; Tapscott Stephen J.; Voermans Nicol C.; Tawil Rabi N.
Chromosome 10q-linked FSHD identifies DUX4 as principal disease gene
2022 ►
Klančar Gašper; Blatnik Ana; Šetrajčič Dragoš Vita; Vogrič Vesna; Stegel Vida; Blatnik Olga; Drev Primož; Gazić Barbara; Krajc Mateja; Novaković Srdjan
A novel germline MLH1 in-frame deletion in a Slovenian Lynch syndrome family associated with uncommon isolated PMS2 loss in tumor tissue
2020 ►
Murch Simon H.; Allen Katrina; Chong Sonny; Amil Dias Jorge; Papadopulou Alexandra; Orel Rok
Potential for improving therapy and defining new research targets in eosinophilic oesophagitis based on understanding of immunopathogenesis
2013 ►
Beraković Doroteja; Videtič Paska Alja
Single nucleotide polymorphisms in the GABRG2, GRIN2B and ODC1 genes and Slovenian suicide victims
[Polimorfizmi s jednim nukleotidom u GABRG2, GRIN2B I ODC1 genima i slovenske žrtve samoubojstva]
2022 ►
Vogrinc David; Goričar Katja; Čučnik Saša; Emeršič Andreja; Gregorič Kramberger Milica; Dolžan Vita
Polymorphisms in oxidative stress response genes as biomarkers in Alzheimer’s disease
2022 ►
Urh Kristian; Zidar Nina; Boštjančič Emanuela
Identification and validation of stem cell-related genes in colorectal cancerogenesis
2022 ►
Goričar Katja; Marinko Tanja; Dolžan Vita
Biomarkers of radiotherapy response in breast cancer reporter genes in two murine tumor cell lines in vitro
2022 ►
Komel Tilen; Bošnjak Maša; Serša Gregor; Čemažar Maja
Concomitant gene electrotransfer of plasmids encoding GFP and DsRed reporter genes in two murine tumor cell lines in vitro
2022 ►
Gros Katarina; Matkovič Urška; Parato Giulia; Miš Katarina; Luin Elisa; Bernareggi Annalisa; Sciancalepore Marina; Marš Tomaž; Lorenzon Paola; Pirkmajer Sergej
Neuronal agrin promotes proliferation of primary human myoblasts in an age-dependent manner
2022 ►
Zlodej Špela; Ficko Maja; Avbelj Stefanija Magdalena; Trebušak Podkrajšek Katarina; Hovnik Tinka
Analiza sprememb v številu kopij genov povezanih s hipogonadotropnim hipogonadizmom z metodo MLPA
[Analysis of copy number variaton in genes connected with hypogonadotropic hypogonadism by MLPA]
2022 ►
Štok Ula; Štucin Neža; Blokar Elizabeta; Ambrožič Aleš; Sodin-Šemrl Snežna; Čučnik Saša; Žigon Polona
Antiphospholipid antibody syndrome-associated increased surface expression of VLA4 integrin on human monocytes
2022 ►
Jurgec Staša; Jezernik Gregor; Gorenjak Mario; Büdefeld Tomaž; Potočnik Uroš
Meta-analytic comparison of global RNA transcriptomes of acute and chronic myeloid leukemia cells reveals novel gene candidates governing myeloid malignancies
2022 ►
Goričar Katja; Dugar Franja; Dolžan Vita; Marinko Tanja
NBN, RAD51 and XRCC3 polymorphisms as potential predictive biomarkers of adjuvant radiotherapy toxicity in early HER2-positive breast cancer
2022 ►
Marmolejo David Humberto; Zheng Wong Mark Yu; Bajalica-Lagercrantz Svetlana; Tischkowitz Marc; Balmaña Judith; Balázs Patócs Attila; Colas Chrystelle; Genuardi Maurizio; Klink Barbara; Krajc Mateja
Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe
2021 ►
Ranković Branislava; Boštjančič Emanuela; Zidar Nina; Žlajpah Margareta; Jeruc Jera
miR-200b, ZEB2 and PTPN13 are downregulated in colorectal carcinoma with serosal invasion
2022 ►
Zavrtanik Hana; Luzar Boštjan; Tomažič Aleš
Intra-ampullary papillary-tubular neoplasm combined with ampullary neuroendocrine carcinoma
2022 ►
Razpotnik Rok; Vidmar Robert; Fonović Marko; Rozman Damjana; Režen Tadeja
Circular RNA hsa_circ_0062682 binds to YBX1 and promotes oncogenesis in hepatocellular carcinoma
2022 ►
Chikhaou Asma; Jones Meriem; Režen Tadeja; Ben Ahmed Melika; Naouali Chokri; Komel Radovan; Zghal Mohamed; Boubaker Samir; Abdelhak Sonia; Yacoub-Youssef Houda
Inflammatory landscape in Xeroderma pigmentosum patients with cutaneous melanoma
2022 ►
Urh Kristian; Zidar Nina; Tomažič Aleš; Boštjančič Emanuela
Intra-tumor heterogeneity of cancer stem cell-related genes and their potential regulatory microRNAs in metastasizing colorectal carcinoma
2022 ►
Vrščaj Lucija Ana; Marc Janja; Ostanek Barbara
Interactome of PTH-Regulated miRNAs and their predicted target genes for Investigating the epigenetic effects of PTH (1‐34) in bone metabolism
2022 ►
Bedenk Jure; Režen Tadeja; Jančar Nina; Geršak Ksenija; Virant-Klun Irma
Effect of in vitro maturation of human oocytes obtained after controlled ovarian hormonal stimulation on the expression of development- and zona pellucida-related genes and their interactions
2022 ►
Kuret Tadeja; Peskar Dominika; Erdani-Kreft Mateja; Erman Andreja; Veranič Peter
Comprehensive transcriptome profiling of urothelial cells following TNFα stimulation in an in vitro interstitial cystitis/bladder pain syndrome model
2022 ►
Zupanič-Pajnič Irena; Zupanc Tomaž; Leskovar Tamara; Črešnar Matija; Fattorini Paolo
Eye and hair color prediction of ancient and second world war skeletal remains using a forensic PCR-MPS approach
2022 ►
Vičič Žiga; Skubic Cene; Walakira Andrew; Rozman Damjana
Comparing the results of expression of differentially expressed genes determined by oxford nanopore sequencing and DNA-microarrays with QPCR in hepatoma HEPG2 cells with SC5D knockout
2022 ►
Nikolac Perković Matea; Kouter Katarina; Švob Štrac Dubravka; Katrašnik Mojca; Uzun Suzana; Kozumplik Oliver; Mimica Ninoslav; Pivac Nela; Videtič Paska Alja
DNA methylation of candidate genes BDNF and COMT in Alzheimer’s disease
2021 ►
Flores Ana I.; Pipino Caterina; Dragin Jerman Urška; Liarte Sergio; Gindraux Florelle; Erdani-Kreft Mateja; Nicolas Francisco J.; Pandolfi Assunta; Tratnjek Larisa; Giebel Bernd
Perinatal derivatives
2022 ►
Kramar Barbara; Pirc Marolt Tinkara; Monsalve Maria; Šuput Dušan; Milisav Irina
Antipsychotic drug aripiprazole protects liver cells from oxidative stress
2022 ►
Škrgat Sabina; Košnik Mitja; Popović-Grle Sanja
Severe asthma - basic and clinical views
2022 ►
Kuralt Hojka; Fidler Aleš; Blatnik Ana; Novaković Srdjan; Plavc Gaber
Bilateral parotid glands aplasia
2022 ►
Štampar Patricija; Petrovič Uroš; Magdevska Vasilka; Žgur-Bertok Darja; Butala Matej
Izražanje genov za biosintezo likopena v kvasovki Yarrowia lipolytica
[Expression of lycopene biosynthesis genes in yeast Yarrowia lipolytica]
2019 ►
Sharma Kuldeepak; Erdani-Kreft Mateja; Škufca Sterle Mateja; Vasić Darko
Role of microbiome in inflammation during tuberculosis
2022 ►
Gupta Gaurav; Oliver Brian G.; Dua Kamal; Singh Alisha; MacLoughlin Ronan
Microbiome in inflammatory lung diseases
2022 ►
Disha Ibrahimi Saranda; Furlani Borut; Drevenšek Gorazd; Hudoklin Samo; Marc Janja; Prodan Žitnik Irena; Sajovic Jakob; Drevenšek Martina
Olanzapine decreased osteocyte maturation and Wnt/β-catenin signaling during loading of the alveolar bone in rats
2022 ►
Leban Tina; Trebušak Podkrajšek Katarina; Kovač Jernej; Fidler Aleš; Pavlič Alenka
An intron c.103-3T>C variant of the AMELX gene causes combined hypomineralized and hypoplastic type of amelogenesis imperfecta
2022 ►
Hrovat Katja; Rehberger Likozar Andreja; Zupan Janja; Šebeštjen Miran
Gene expression profiling of markers of inflammation, angiogenesis, coagulation and fibrinolysis in patients with coronary artery disease with very high lipoprotein(a) levels treated with PCSK9 inhibitors
2022 ►
Ružić-Sabljić Eva; Ðaković-Rode Oktavija
Zamke i dobrobiti serološke dijagnostike lajmske borelioze iz laboratorijske perspektive
[Pitfalls and benefits of serological diagnosis of lyme borreliosis from a laboratory perspective]
2021 ►
Pavlič Ana; Hauptman Nina; Boštjančič Emanuela; Zidar Nina
Long non-coding RNAs as potential regulators of EMT-related transcription factors in colorectal cancer
2022 ►
Drnovšek Eva; Jensterle Sever Mojca; Goričar Katja; Redenšek Sara; Janež Andrej; Milisav Irina; Dolžan Vita
Genetic variability in the cholecystokinin A receptor affects lipid profile and glucose tolerance in patients with polycystic ovary syndrome
2022 ►
Jevnikar Kristina; Lapajne Luka; Petrovič Danijel; Meglič Andrej; Logar Mateja; Vidović Valentinčič Nataša; Globočnik Petrovič Mojca; Cilenšek Ines; Jaki Mekjavić Polona
The role of ACE, ACE2, and AGTR2 polymorphisms in COVID-19 severity and the presence of COVID-19-related retinopathy
2022 ►
Stavber Lana; Gaia Maria Joao; Hovnik Tinka; Jenko Bizjan Barbara; Debeljak Maruša; Kovač Jernej; Šuput Jasna; Battelino Tadej; Kotnik Primož; Dovč Klemen
Heterozygous NPR2 variants in idiopathic short stature
2022 ►
Krgović Danijela; Gorenjak Mario; Rihar Nika; Opalič Iva; Stangler Herodež Špela; Gregorič Kumperščak Hojka; Dovč Peter; Kokalj-Vokač Nadja
Impaired neurodevelopmental genes in Slovenian autistic children elucidate the comorbidity of autism with other developmental disorders
2022 ►
Sobočan Monika; Brunialti Daniela; Sprung S; Schatz Christoph; Knez Jure; Kavalar Rajko; Takač Iztok; Haybaeck Johannes
Initiation and elongation factor co-expression correlates with recurrence and survival in epithelial ovarian cancer
2022 ►
Štunf Špela
Are miRNAs dynamic biomarkers in keratoconus?
2022 ►
Ledinek Živa; Sobočan Monika; Knez Jure
The role of CTNNB1 in endometrial cancer
2022 ►
Hovnik Tinka; Žitnik Eva; Avbelj Stefanija Magdalena; Bertok Sara; Sedej Katarina; Bančič Vesna; Battelino Tadej; Grošelj Urh
An adolescent boy with Klinefelter syndrome and 47,XXY/46,XX mosaicism
2022 ►
Bombač Alenka; Zakotnik Branko; Bučić Marina; Šetrajčič Dragoš Vita; Gazić Barbara; Stegel Vida; Klančar Gašper; Novaković Srdjan
Mutational spectrum and classification of novel mutations in patients with metastatic gastrointestinal stromal tumours
2020 ►
Mlekuš Katarina; Kocjan Tomaž; Lanišnik-Rižner Tea
Pregled razvoja metod za določanje vitamina D v krvi
[Development of methods for the measurement of vitamin D in blood ‐ review]
2022 ►
Sotlar Inge; Levstek Tina; Podkrajšek Nik; Rojnik Tamara; Šebeštjen Miran; Rehberger Likozar Andreja; Trebušak Podkrajšek Katarina
Genetic variability in CRP, TNFA, AND IL6 genes and its association with inflammatory markers in patients with very high lipoprotein(a) levels after treatment with PCSK9 inhibitors
2022 ►
Gruenberger Michael; Alberts Rudi; Smedley Damian; Swertz Morris A.; Schofield Paul N.; Schughart Klaus; Hancock John M.
Towards the integration of mouse databases - definition and implementation of solutions to two use-cases in mouse functional genomics
2010 ►
Hrabě de Angelis Martin; Chambon Jean-Pierre; Brown Stephen D.
Standards of mouse model phenotyping
2006 ►
Hancock John M.; Adams Niels C.; Aidinis Vassilis; Blake Andrew
Integration of mouse phenome data resources
2007 ►
Brown Steve D. M.; Hancock John M.
The mouse genome
2006 ►
Hancock John M.; Gates Hilary
The informatics of high-throughput mouse phenotyping
2011 ►
Hancock John M.; Dover Gabriel A.
Paradoxes of molecular coevolution in the rDNA multigene family
1989 ►
Videtič Paska Alja; Nikolac Perković Matea; Kouter Katarina; Švob Štrac Dubravka; Katrašnik Mojca; Uzun Suzana; Kozumplik Oliver; Mimica Ninoslav; Pivac Nela
DNA methylation of candidate genes in Alzheimer’s disease
2022 ►
Zakotnik Samo; Knap Nataša; Bogovič Petra; Zorec Tomaž Mark; Poljak Mario; Strle Franc; Avšič-Županc Tatjana; Korva Miša
Complete genome sequencing of tick-borne encephalitis virus directly from clinical samples
2022 ►
Brown Steve D. M.; Wurst Wolfgang; Kühn Ralf; Hancock John M.
The functional annotation of mammalian genomes
2009 ►
Hancock John M.; Mallon Ann-Marie; Beck Tim; Gkoutos Georgios V.; Mungall Chris; Schofield Paul N.
Mouse, man, and meaning
2009 ►
Smedley Damian; Swertz Morris A.; Wolstencroft Katy; Proctor Glenn; Zouberakis Michael; Bard Jonathan; Hancock John M.; Schofield Paul N.
Solutions for data integration in functional genomics
2008 ►
Blagotinšek Cokan Kaja; Perše Martina; Hancock John M.; Spindelböck Walter; Režen Tadeja; Juvan Peter; Rozman Damjana
Translation of mouse model genetic signatures to human hepatocarcinogenesis
2022 ►
Hancock John M.; Mallon Ann-Marie
Phenobabelomics - mouse phenotype data resources
2007 ►
Hancock John M.
Gene factories, microfunctionalization and the evolution of gene families
2005 ►
Hancock John M.; Simon Michelle M
Simple sequence repeats in proteins and their significance for network evolution
2005 ►
Mallon Ann-Marie; Wilming Laurens; Weekes Joseph; Gilbert James G. R.; Ashurst Jennifer; Peyrefitte Sandrine; Matthews Lucy; Cadman Matthew; McKeone Richard; Hancock John M.
Organization and evolution of a gene-rich region of the mouse genome
2004 ►
Santibáñez-Koref Mauro F.; Gangeswaran Rathithevy; Santibañez Koref I. P.; Shanahan N.; Hancock John M.
A phylogenetic approach to assessing the significance of missense mutations in disease genes
2003 ►
Hancock John M.; Worthey Elisabeth A.; Santibáñez-Koref Mauro F.
A role for selection in regulating the evolutionary emergence of disease- causing and other coding CAG repeats in humans and mice
2001 ►
Albà M. Mar; Santibáñez-Koref Mauro F.; Hancock John M.
The comparative genomics of polyglutamine repeats: extreme differences in the codon organization of repeat-encoding regions between mammals and Drosophila
2001 ►
Mann Christopher J.; Anderson Timothy A.; Read Jacqueline; Chester Ann; Harrison Georgina B.; Köchl Silvano; Ritchie Penelope J.; Hancock John M.
The structure of vitellogenin provides a molecular model for the assembly and secretion of atherogenic lipoproteins
1999 ►
Hancock John M.
Simple sequences and the expanding genome
1996 ►
Djian Philippe; Hancock John M.; Chana Harjinder S.
Codon repeats in genes associated with human diseases
1996 ►
Hancock John M.; Chaleeprom Witcha; Chaleeprom Worawan; Dale James; Gibbs Adrian J.
Replication slippage in the evolution of potyviruses
1995 ►
Hancock John M.
Evolution of sequence repetition and gene duplications in the TATA-binding protein TBP (TFIID)
1993 ►
Linares Andrés Ruiz; Hancock John M.; Dover Gabriel A.
Secondary structure constraints on the evolution of Drosophila 28 S ribosomal RNA expansion segments
1994 ►
Hancock John M.; Dover Gabriel A.
Molecular coevolution among cryptically simple expansion segments of eukaryotic 26S/28S rRNAs
1988 ►
Tautz Diethard; Hancock John M.; Webb David A.; Tautz Christiane; Dover Gabriel A.
Complete sequences of the rRNA genes of Drosophila melanogaster
1988 ►
Hancock John M.; Wagner Rolf
A structural model of 5S RNA from E. coli based on intramolecular crosslinking evidence
1982 ►
Iosifidis Christos; Liu Jingshu; Gale Theodora; Ellingford Jamie M; Campbell Christopher; Ingram Stuart; Chandler Kate; Parry Neil R.A.; Black Graeme C. M.; Sergouniotis Panagiotis I.
Clinical and genetic findings in TRPM1-related congenital stationary night blindness
2022 ►
Hancock John M.; Dover Gabriel A.
'Compensatory slippage' in the evolution of ribosomal RNA genes
1990 ►
Karas Kuželički Nataša; Šmid Alenka; Vidmar Maša; Kek Tina; Geršak Borut; Mazić Uroš; Mlinarič-Raščan Irena; Geršak Ksenija
A common polymorphism in the MTHFD1 gene is a modulator of risk of congenital heart disease
2022 ►
Šket Robert; Kotnik Primož; Jenko Bizjan Barbara; Kocen Valentina; Mlinarič Matej; Tesovnik Tine; Debeljak Maruša; Battelino Tadej; Kovač Jernej
Heterozygous genetic variants in autosomal recessive genes of the leptin-melanocortin signalling pathway are associated with the development of childhood obesity
2022 ►
Filipič Bratko; Gradišnik Lidija; Pereyra Gonzales Adriana; Mazija Hrvoje
The immunomodulatory activity in-vitro of NDV ZG1999HDS in comparison to NDV La Sota
2022 ►
Ravnik-Glavač Metka; Goričar Katja; Vogrinc David; Koritnik Blaž; Lavrenčič Jakob Gašper; Glavač Damjan; Dolžan Vita
Genetic variability of inflammation and oxidative stress genes affects onset, progression of the disease and survival of patients with amyotrophic lateral sclerosis
2022 ►
Lacovich Valentina; Espindola Sonia L.; Alloatti Matías; Pozo Devoto Victorio Martin; Cromberg Lucas E.; Čarná Mária; Forte Giancarlo; Gallo Jean-Marc; Bruno Luciana; Stokin Gorazd Bernard
Tau isoforms imbalance impairs the axonal transport of the amyloid precursor protein in human neurons
2017 ►
Nardone Giorgia; Oliver-De La Cruz Jorge; Vrbsky Jan; Martini Cecilia; Přibyl Jan; Skládal Petr; Pešl Martin; Caluori Guido; Stokin Gorazd Bernard
YAP regulates cell mechanics by controlling focal adhesion assembly
2017 ►
Švajger Urban; Cukjati Marko
Zdravila za napredno zdravljenje
[Advanced therapy medicinal products]
2022 ►
Onyango Isaac G.; Bennett James P.; Stokin Gorazd Bernard
Mitochondrially-targeted therapeutic strategies for Alzheimer's disease
2021 ►
Onyango Isaac G.; Bennett James P.; Stokin Gorazd Bernard
Regulation of neuronal bioenergetics as a therapeutic strategy in neurodegenerative diseases
2021 ►
Green David J.; Lenassi Eva; Manning Cerys S.; McGaughey David; Sharma Vinod; Black Graeme C. M.; Ellingford Jamie M; Sergouniotis Panagiotis I.
North Carolina macular dystrophy
2021 ►
Moškrič Ajda; Marinč Andraž; Ferk Polonca; Leskošek Branimir; Mosbech Mai-Britt; Bunikis Ignas; Vinnere Pettersson Olga; Soler Lucile; Prešern Janez
The Carniolan honeybee from Slovenia
2022 ►
Levstek Tina; Podkrajšek Nik; Rehberger Likozar Andreja; Šebeštjen Miran; Trebušak Podkrajšek Katarina
The influence of treatment with PCSK9 inhibitors and variants in the CRP (rs1800947), TNFA (rs1800629), and IL6 (rs1800795) genes on the corresponding inflammatory markers in patients with very high lipoprotein(a) levels
2022 ►
Krašovec Tjaša; Šikonja Jaka; Žerjav-Tanšek Mojca; Debeljak Maruša; Ilovar Saša; Trebušak Podkrajšek Katarina; Bertok Sara; Tesovnik Tine; Kovač Jernej; Šuput Jasna; Hartmann Michaela F.; Wudy Stefan A; Avbelj Stefanija Magdalena; Battelino Tadej; Kotnik Primož; Grošelj Urh
Long-term follow-up of three family members with a novel NNT pathogenic variant causing primary adrenal insufficiency
2022 ►
Režen Tadeja; Rozman Damjana; Kovács Tünde; Kovács Patrik; Sipos Adrienn; Bai Péter; Mikó Edit
The role of bile acids in carcinogenesis
2022 ►
Zajec Ana; Trebušak Podkrajšek Katarina; Tesovnik Tine; Šket Robert; Čugalj Kern Barbara; Jenko Bizjan Barbara; Šmigoc Schweiger Darja; Battelino Tadej; Kovač Jernej
Pathogenesis of type 1 diabetes
2022 ►

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