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PLoS ONE, ISSN 1932-6203, 09/2016, Volume 11, Issue 9, pp. e0162866 - e0162866
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 01/2016, Volume 24, Issue 1, pp. 66 - 72
Journal Article
FORESTS, ISSN 1999-4907, 08/2019, Volume 10, Issue 8, p. 634
In temperate regions of Europe, the large pine weevil, Hylobius abietis, is a major pest of coniferous forests mostly at sites where clear-felling is followed... 
entomopathogenic fungi | PERSISTENCE | LARGE PINE WEEVIL | BEAUVERIA-BASSIANA | L COL | virulence | Hypocreales | Hylobius abietis | CONIFER SEEDLINGS | SP-NOV | COLEOPTERA-CURCULIONIDAE | NOMURAEA-RILEYI | FORESTRY | BIOLOGICAL-CONTROL | biocontrol
Journal Article
Neuroscience Letters, ISSN 0304-3940, 2011, Volume 498, Issue 2, pp. 138 - 142
Journal Article
Clinical Genetics, ISSN 0009-9163, 02/2017, Volume 91, Issue 2, pp. 339 - 343
Say–Barber–Biesecker–Young–Simpson syndrome (SBBYSS) and genitopatellar syndrome (GTPTS) are clinically similar disorders with some overlapping features.... 
Say–Barber–Biesecker–Young–Simpson syndrome, SBBYSS | KAT6B | lysine acetyltransferase 6B | genitopatellar syndrome | KAT6B spectrum disorders | GTPTS | KAT6B‐related disorders | KAT6B-related disorders | BLEPHAROPHIMOSIS | HISTONE ACETYLTRANSFERASE | FEATURES | RETARDATION | Say-Barber-Biesecker-Young-Simpson syndrome, SBBYSS | GENETICS & HEREDITY | MUTATIONS | SPECTRUM | Abnormalities, Multiple - pathology | Scrotum - abnormalities | Kidney - pathology | Exons | Humans | Joint Instability - genetics | Child, Preschool | Histone Acetyltransferases - genetics | Joint Instability - pathology | Blepharophimosis - pathology | Intellectual Disability - genetics | Blepharophimosis - genetics | Heart Defects, Congenital - genetics | Psychomotor Disorders - genetics | Congenital Hypothyroidism - diagnosis | Blepharophimosis - diagnosis | Congenital Hypothyroidism - genetics | Facies | Patella - abnormalities | Craniofacial Abnormalities - pathology | Female | Scrotum - pathology | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Joint Instability - diagnosis | Urogenital Abnormalities - diagnosis | Heart Defects, Congenital - pathology | Intellectual Disability - pathology | Psychomotor Disorders - pathology | Patella - pathology | Phenotype | Urogenital Abnormalities - pathology | Craniofacial Abnormalities - diagnosis | Kidney - abnormalities | Abnormalities, Multiple - diagnosis | Intellectual Disability - diagnosis | Psychomotor Disorders - diagnosis | Congenital Hypothyroidism - pathology | Heart Defects, Congenital - diagnosis | Mutation | Urogenital Abnormalities - genetics | Genetic disorders | Multiprocessing | Lysine | Genetic aspects | Nucleotide sequencing | DNA sequencing | Genotype & phenotype
Journal Article
Acta Facultatis Pharmaceuticae Universitatis Comenianae, ISSN 0301-2298, 12/2015, Volume 62, Issue 11, pp. 2 - 7
Genetic diagnostics of hereditary breast and ovarian cancer (HBOC) has been performed in Slovakia in many different forms before the year 2000. Complex HBOC... 
clinical management | klinický manažment | direct sequencing | priame sekvenovanie | pathological mutation | BRCA1 | BRCA2 | hereditárny karcinóm prsníka a ovárií | patologická mutácia | Hereditary Breast Ovarian Cancer
Journal Article
Journal of Neurosurgery, ISSN 0022-3085, 07/2013, Volume 119, Issue 1, pp. 172 - 179
Object. Wall shear stress (WSS) plays a role in regulating endothelial function and has been suspected in cerebral aneurysm rupture. The aim of this study was... 
Intraoperative microscopy | Aneurysm | Shear stress | Hemodynamics | Wall thickness | Pressure | Vascular disorders | SURGERY | aneurysm | ATHEROSCLEROSIS | CELL-PROLIFERATION | pressure | BLOOD-FLOW | hemodynamics | vascular disorders | CLINICAL NEUROLOGY | intraoperative microscopy | shear stress | wall thickness | INTRACRANIAL ANEURYSMS | GROWTH | SUBARACHNOID HEMORRHAGE | RUPTURE | ARTERY | EXPRESSION | BIFURCATION
Journal Article
GENES, ISSN 2073-4425, 06/2019, Volume 10, Issue 6, p. 459
The molecular genetics of well-characterized inherited diseases, such as phenylketonuria (PKU) and hyperphenylalaninemia (HPA) predominantly caused by... 
MOLECULAR-GENETICS | functional studies | phenylalanine hydroxylase | GENOTYPE | STABILITY | PHENOTYPE | CLASSIFICATION | BH4 | HYPERPHENYLALANINEMIA | GENETICS & HEREDITY | TETRAHYDROBIOPTERIN | MUTATIONS | phenylketonuria | EXPRESSION | missense variants
Journal Article