Search Results - "Jelena Martinovic"
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Role of Ectonucleotidases in Synapse Formation During Brain Development: Physiological and Pathological Implications
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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2
FGF9 and FGF20 Maintain the Stemness of Nephron Progenitors in Mice and Man
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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3
Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract
Published in Journal of the American Society of Nephrology (01-10-2017)“…Congenital anomalies of the kidney and urinary tract (CAKUT) occur in three to six of 1000 live births, represent about 20% of the prenatally detected…”
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4
Loss of function mutations in EPHB4 are responsible for vein of Galen aneurysmal malformation
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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5
Progesterone Protects Prefrontal Cortex in Rat Model of Permanent Bilateral Common Carotid Occlusion via Progesterone Receptors and Akt/Erk/eNOS
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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6
Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system
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
Published in Pediatric nephrology (Berlin, West) (2012)“…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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Developmental interplay between transcriptional alterations and a targetable cytokine signaling dependency in pediatric ETO2::GLIS2 leukemia
Published in Molecular cancer (20-09-2024)“…Several fusion oncogenes showing a higher incidence in pediatric acute myeloid leukemia (AML) are associated with heterogeneous megakaryoblastic and other…”
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Discriminant analysis of cardiovascular and respiratory variables for classification of road cyclists by specialty
Published in Journal of sports medicine and physical fitness (01-06-2019)“…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
Published in American journal of obstetrics and gynecology (01-01-2018)“…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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11
DYNC2H1 Mutations Cause Asphyxiating Thoracic Dystrophy and Short Rib-Polydactyly Syndrome, Type III
Published in American journal of human genetics (15-05-2009)“…Jeune asphyxiating thoracic dystrophy (ATD) is an autosomal-recessive chondrodysplasia characterized by short ribs and a narrow thorax, short long bones,…”
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12
Prolonged Alprazolam Treatment Alters Components of Glutamatergic Neurotransmission in the Hippocampus of Male Wistar Rats-The Neuroadaptive Changes following Long-Term Benzodiazepine (Mis)Use
Published in Pharmaceuticals (Basel, Switzerland) (21-02-2023)“…Alprazolam (ALP), a benzodiazepine (BDZ) used to treat anxiety, panic, and sleep disorders, is one of the most prescribed psychotropic drugs worldwide. The…”
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13
A retrospective study on the efficacy of prenatal diagnosis for pregnancies at risk of mitochondrial DNA disorders
Published in Genetics in medicine (01-04-2021)“…Prenatal diagnosis of mitochondrial DNA (mtDNA) disorders is challenging due to potential instability of fetal mutant loads and paucity of data connecting…”
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14
Analysis of human samples reveals impaired SHH-dependent cerebellar development in Joubert syndrome/Meckel syndrome
Published in Proceedings of the National Academy of Sciences - PNAS (16-10-2012)“…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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15
Severe Prenatal Renal Anomalies Associated with Mutations in HNF1B or PAX2 Genes
Published in Clinical journal of the American Society of Nephrology (01-07-2013)“…Congenital anomalies of the kidney and urinary tract (CAKUT) are a frequent cause of renal failure in children, and their detection in utero is now common with…”
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The male external urethral sphincter is autonomically innervated
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
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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18
Evaluation of different formulas for LDL-C calculation
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
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
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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