Search Results - "Jelena Martinovic"

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    Role of Ectonucleotidases in Synapse Formation During Brain Development: Physiological and Pathological Implications by Ivana Grković, Dunja Drakulić, Jelena Martinović, Nataša Mitrović

    Published in Current neuropharmacology (01-01-2019)
    “…Background: Extracellular adenine nucleotides and nucleosides, such as ATP and adenosine, are among the most recently identified and least investigated…”
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    FGF9 and FGF20 Maintain the Stemness of Nephron Progenitors in Mice and Man by Barak, Hila, Huh, Sung-Ho, Chen, Shuang, Jeanpierre, Cécile, Martinovic, Jelena, Parisot, Mélanie, Bole-Feysot, Christine, Nitschké, Patrick, Salomon, Rémi, Antignac, Corinne, Ornitz, David M., Kopan, Raphael

    Published in Developmental cell (12-06-2012)
    “…The identity of niche signals necessary to maintain embryonic nephron progenitors is unclear. Here we provide evidence that Fgf20 and Fgf9, expressed in the…”
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    Loss of function mutations in EPHB4 are responsible for vein of Galen aneurysmal malformation by Vivanti, Alexandre, Ozanne, Augustin, Grondin, Cynthia, Saliou, Guillaume, Quevarec, Loic, Maurey, Helène, Aubourg, Patrick, Benachi, Alexandra, Gut, Marta, Gut, Ivo, Martinovic, Jelena, Sénat, Marie Victoire, Tawk, Marcel, Melki, Judith

    Published in Brain (London, England : 1878) (01-04-2018)
    “…See Meschia (doi:10.1093/brain/awy066) for a scientific commentary on this article. The vein of Galen aneurysmal malformation is one of the most frequent…”
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    Progesterone Protects Prefrontal Cortex in Rat Model of Permanent Bilateral Common Carotid Occlusion via Progesterone Receptors and Akt/Erk/eNOS by Stanojlović, Miloš, Guševac Stojanović, Ivana, Zarić, Marina, Martinović, Jelena, Mitrović, Nataša, Grković, Ivana, Drakulić, Dunja

    Published in Cellular and molecular neurobiology (01-07-2020)
    “…Sustained activation of pro-apoptotic signaling due to a sudden and prolonged disturbance of cerebral blood circulation governs the neurodegenerative processes…”
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    Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system by Monnot, Sophie, Gigarel, Nadine, Samuels, David C., Burlet, Philippe, Hesters, Laetitia, Frydman, Nelly, Frydman, René, Kerbrat, Violaine, Funalot, Benoit, Martinovic, Jelena, Benachi, Alexandra, Feingold, Josué, Munnich, Arnold, Bonnefont, Jean-Paul, Steffann, Julie

    Published in Human mutation (01-01-2011)
    “…Mitochondrial DNA (mtDNA) mutations cause a wide range of serious diseases with high transmission risk and maternal inheritance. Tissue heterogeneity of the…”
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    Phenotypic variability of Bardet-Biedl syndrome: focusing on the kidney by Putoux, Audrey, Attie-Bitach, Tania, Martinovic, Jéléna, Gubler, Marie-Claire

    “…Bardet-Biedl syndrome (BBS) is a multisystemic developmental disorder diagnosed on the basis of the presence of obesity, retinal defects, polydactyly,…”
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    Discriminant analysis of cardiovascular and respiratory variables for classification of road cyclists by specialty by Nikolić, Biljana, Martinović, Jelena, Matić, Milan, Stefanović, Đorđe

    “…BACKGROUND: Different variables determine the performance of cyclists, which brings up the question how these parameters may help in their classification by…”
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    Detailed muscular structure and neural control anatomy of the levator ani muscle: a study based on female human fetuses by Nyangoh Timoh, Krystel, Moszkowicz, David, Zaitouna, Mazen, Lebacle, Cedric, Martinovic, Jelena, Diallo, Djibril, Creze, Maud, Lavoue, Vincent, Darai, Emile, Benoit, Gérard, Bessede, Thomas

    “…Injury to the levator ani muscle or pelvic nerves during pregnancy and vaginal delivery is responsible for pelvic floor dysfunction. We sought to demonstrate…”
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    Analysis of human samples reveals impaired SHH-dependent cerebellar development in Joubert syndrome/Meckel syndrome by Aguilar, Andrea, Meunier, Alice, Strehl, Laetitia, Martinovic, Jelena, Bonniere, Maryse, Attie-Bitach, Tania, Encha-Razavi, Féréchté, Spassky, Nathalie

    “…Joubert syndrome (JS) and Meckel syndrome (MKS) are pleiotropic ciliopathies characterized by severe defects of the cerebellar vermis, ranging from hypoplasia…”
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    The male external urethral sphincter is autonomically innervated by Nyangoh Timoh, Krystel, Moszkowicz, David, Creze, Maud, Zaitouna, Mazen, Felber, Margaux, Lebacle, Cédric, Diallo, Djibril, Martinovic, Jelena, Tewari, Ashutosh, Lavoué, Vincent, Ghukasyan, Gevorg, Benoit, Gerard, Bessede, Thomas

    Published in Clinical anatomy (New York, N.Y.) (01-03-2021)
    “…Introduction The aim of the present study was to describe autonomic urethral sphincter (US) innervation using specific muscular and neuronal antibody markers…”
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    Prolonged Zaleplon Treatment Increases the Expression of Proteins Involved in GABAergic and Glutamatergic Signaling in the Rat Hippocampus by Martinovic, Jelena, Samardzic, Janko, Zaric Kontic, Marina, Ivkovic, Sanja, Dacic, Sanja, Major, Tamara, Radosavljevic, Milica, Svob Strac, Dubravka

    Published in Brain sciences (01-12-2023)
    “…Zaleplon is a positive allosteric modulator of the γ-aminobutyric acid (GABA) receptor approved for the short-term treatment of insomnia. Previous publications…”
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    Evaluation of different formulas for LDL-C calculation by Vujovic, Ana, Kotur-Stevuljevic, Jelena, Spasic, Slavica, Bujisic, Nada, Martinovic, Jelena, Vujovic, Milica, Spasojevic-Kalimanovska, Vesna, Zeljkovic, Aleksandra, Pajic, Dragoljub

    Published in Lipids in health and disease (10-03-2010)
    “…Friedewald's formula for the estimation of LDL-C concentration is the most often used formula in clinical practice. A recent formula by Anandaraja and…”
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    Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations by Van‐Gils, Julien, Naudion, Sophie, Toutain, Jérôme, Lancelot, Gwenaelle, Attié‐Bitach, Tania, Blesson, Sophie, Demeer, Bénédicte, Doray, Bérénice, Gonzales, Marie, Martinovic, Jelena, Whalen, Sandra, Taine, Laurence, Arveiler, Benoit, Lacombe, Didier, Fergelot, Patricia

    Published in Clinical genetics (01-03-2019)
    “…Rubinstein‐Taybi syndrome (RSTS; OMIM 180849) is an autosomal dominant developmental disorder characterized by facial dysmorphism, broad thumbs and halluces…”
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    Impact of educational intervention for correct inhaler technique on the quality of life of children with asthma by Konevic, Slavica, Djonovic, Nela, Djuric, Dusan, Markovic-Denic, Ljiljana, Vasic, Dobrila, Martinovic, Jelena

    Published in Vojnosanitetski pregled (2020)
    “…Background/Aim. Asthma is the most common chronic disease in children and adolescents and has shown an apparent increase in incidence in recent years. The…”
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