Frequency of galactose-1-phosphate uridyl transferase gene mutations in healthy population of Croatia [PDF]
, 2008 Galactosemia is a human disease caused by deficient activity of each one of the three enzymes involved in galactose metabolism, galactokinase (GALK), galactose-1-phosphate uridyl transferase (GALT) and UDP-galactose-4-epimerase (GALE).
Barišić, Karmela +3 more
core +3 more sources
Different metabolic features 1 of Bacteroides fragilis growing in the presence of glucose and exopolysaccharides of bifidobacteria [PDF]
, 2017 Bacteroides is among the most abundant microorganism inhabiting the human intestine. They are saccharolytic bacteria able to use dietary or host-derived glycans as energy sources.
González de los Reyes-Gavilán, Clara +6 more
core +1 more source
Cellulóz gének kifejeződése Trichoderma reesei-ben: a laktóz általi indukció mechanizmusa = Cellulase gene expression in Trichoderma reesei: mechanism of lactose induction [PDF]
, 2008 A posztdoktori kutatás során fonalas tömlősgombák laktóz és D-galaktóz anyagcseréjének szabályozási mechanizmusait tanulmányoztuk. Munkánk azon korábbi kutatásaink folytatása volt, melyek során jellemeztük az Aspergillus nidulans béta-galaktozidáz ...
Fekete, Erzsébet
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Community proteogenomics reveals the systemic impact of phosphorus availability on microbial functions in tropical soil. [PDF]
, 2018 Phosphorus is a scarce nutrient in many tropical ecosystems, yet how soil microbial communities cope with growth-limiting phosphorus deficiency at the gene and protein levels remains unknown.
Guo, Xuan +11 more
core +1 more source
Noncoding variation of the gene for ferritin light chain in hereditary and age-related cataract [PDF]
, 2013 PURPOSE: Cataract is a clinically and genetically heterogeneous disorder of the ocular lens and an important cause of visual impairment. The aim of this study was to map and identify the gene underlying autosomal dominant cataract segregating in a four ...
Bennett, Thomas M +5 more
core +2 more sources
Galactose and its Metabolites Deteriorate Metaphase II Mouse Oocyte Quality and Subsequent Embryo Development by Disrupting the Spindle Structure [PDF]
, 2017 Premature ovarian insufficiency (POI) is a frequent long-term complication of classic galactosemia. The majority of women with this disorder develop POI, however rare spontaneous pregnancies have been reported. Here, we evaluate the effect of D-galactose
Abu-Soud, Husam M +7 more
core +2 more sources
The Crabtree effect shapes the Saccharomyces cerevisiae lag phase during the switch between different carbon sources [PDF]
, 2018 When faced with environmental changes, microbes often enter a temporary growth arrest during which they reprogram the expression of specific genes to adapt to the new conditions.
Bisschops, Markus MM +15 more
core +3 more sources
Genetikai kórképek hazai roma populatióban = Genetic disorders in Romani population [PDF]
, 2006 1. Biotinidase defektusos újszülöttek szűrése a betegek molekuláris genetikai analysise magyar kaukazoid és roma populatioban.Eredmények:Hazai vizsgálatok: 58 családban vizsgáltuk a specifikus biotinidáz enzymaktivitást a kiszűrt enzymhiányos családokban,
Béres, Judit +4 more
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Examination of molecular mechanism for metabolism of lactose and D-galactose in the filamentous fungus Aspergillus nidulans [PDF]
, 2016 A bgaD/lacpA génpár élettani induktora a D-galaktóz, és nem a D-galaktóz lebontás valamelyik köztese. A LacpA és a LacpB transzporterek együttesen felelősek a laktóz sejtbe juttatásáért.
Kovácsné Orosz, Anita
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Galactose-1-Phosphate Uridyl Transferase (GALT) and Galactosemia A Review of GALT Function and Current Theories on Galactosemia Pathogenesis [PDF]
, 2014 All living organisms depend on the metabolism of carbohydrates for energy and the biosynthesis of necessary glycoconjugates. One of these carbohydrates is the monosaccharide galactose.
Rehrer, Lydia R
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