Pretraživanje
Prikaz rezultata 1-10 od 286
Procarboxypeptidase U (TAFI) contributes to the risk of thrombosis in patients with hereditary thrombophilia
(Pergamon-Elsevier Science Ltd, Oxford, 2009)
Introduction: It is considered that high plasma levels of procarboxypeptidase U (proCPU or TAFI) can promote the development of thrombosis, but data comparing proCPU levels in thrombophilia carriers and healthy subjects ...
New transcriptional regulatory element within the intron of phenylalanine hydroxylase gene
(Academic Press Inc Elsevier Science, San Diego, 2009)
Acute myeloid leukemia with NUP98-HOXC13 fusion and FLT3 internal tandem duplication mutation: case report and literature review
(Elsevier Science Inc, New York, 2009)
The NUP98 gene at chromosome band 11p15 is known to be fused to a number of different partners in various hematological malignancies. The most frequently observed fusion partners of NUP98 are the homeobox family of ...
Est-ssrs developed for other picea species amplify in picea omorika and reveal high genetic variation in two natural populations
(Soc Royal Botan Belgique, Meise, 2009)
Picea omorika (Pane.) Purk. is a relict and an endemic species found exclusively in the Balkan, within an area of ca. 10 000 km(2). Marker-based genetic diversity data in this conifer are very limited and partially ...
Incidenca hiperhomocisteinemije i polimorfizam MTHFR C677T kod mladih bolesnika sa akutnim infarktom miokarda / Incidence of hyperhomocysteinemia and MTHFR C677T polymorphism among young patients with acute myocardial infarction
(Društvo medicinskih biohemičara Srbije, Beograd i Versita, 2009)
Hiperhomocisteinemija se smatra nezavisnim faktorom rizika za preuranjeni razvoj kardiovaskularnih bolesti. Mutacija MTHFR C677T snižava aktivnost metilentetra hidrofol atreduktaze i može dovesti do hiperhomocisteinemije. ...
Izoelektrofokusiranje i PCR amplifikacija-reverzna hibridizacija u proceni nedostatka alfa-1-antitripsina / Isoelectrofocusing and PCR amplification-reverse hybridization assay in evaluation of alpha-1-antitrypsin deficiency
(Društvo medicinskih biohemičara Srbije, Beograd i Versita, 2009)
Nedostatak alfa-1-antitripsina je potencijalno smrtonosan genetski poremećaj sa pulmonarnim i hepatičnim manifestacijama. Uočljiva je potreba za standardizovanim protokolom detekcije klinički značajnih alela, koji bi ...
GAD isoforms exhibit distinct spatiotemporal expression patterns in the developing mouse lens: Correlation with Dlx2 and Dlx5
(Wiley-Liss, Hoboken, 2007)
Gamma-aminobutyric acid (GABA), the major inhibitory neurotransmitter of the adult nervous system and its biosynthetic enzyme glutamic acid.. decarboxylase (GAD) are abundantly expressed in the embryonic nervous system and ...
Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe
(Springer, New York, 2000)
We report a large genomic deletion of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, viz.. a deletion that is frequently observed in Central and Eastern Europe. The mutation, termed CFTRdele2.3(21 ...
Novel mechanism of bacteriocin secretion and immunity carried out by lactococcal multidrug resistance proteins
(Amer Soc Biochemistry Molecular Biology Inc, Bethesda, 2003)
A natural isolate of Lactococcus lactis was shown to produce two narrow spectrum class II bacteriocins, designated LsbA and LsbB. The cognate genes are located on a 5.6-kb plasmid within a gene cluster specifying LmrB, an ...
The conversion of BTEX compounds by single and defined mixed cultures to medium-chain-length polyhydroxyalkanoate
(Springer, New York, 2008)
Here, we report the use of petrochemical aromatic hydrocarbons as a feedstock for the biotechnological conversion into valuable biodegradable plastic polymers-polyhydroxyalkanoates (PHAs). We assessed the ability of the ...