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See detailGenetical metabolomics of flavonoid biosynthesis in Populus: a case study
Morreel, K.; Goeminne, G.; Storme, V. et al

in Plant Journal (2006), 47(2), 224-237

Genetical metabolomics [metabolite profiling combined with quantitative trait locus (QTL) analysis] has been proposed as a new tool to identify loci that control metabolite abundances. This concept was ... [more ▼]

Genetical metabolomics [metabolite profiling combined with quantitative trait locus (QTL) analysis] has been proposed as a new tool to identify loci that control metabolite abundances. This concept was evaluated in a case study with the model tree Populus. Using HPLC, the peak abundances were analyzed of 15 closely related flavonoids present in apical tissues of two full-sib poplar families, Populus deltoides cv. S9-2 x P. nigra cv. Ghoy and P. deltoides cv. S9-2 x P. trichocarpa cv. V24, and correlation and QTL analysis were used to detect flux control points in flavonoid biosynthesis. Four robust metabolite quantitative trait loci (mQTL), associated with rate-limiting steps in flavonoid biosynthesis, were mapped. Each mQTL was involved in the flux control to one or two flavonoids. Based on the identities of the affected metabolites and the flavonoid pathway structure, a tentative function was assigned to three of these mQTL, and the corresponding candidate genes were mapped. The data indicate that the combination of metabolite profiling with QTL analysis is a valuable tool to identify control points in a complex metabolic pathway of closely related compounds. [less ▲]

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See detailGenetical metabolomics of flavonoid biosynthesis in Populus: a case study.
Morreel, Kris; Goeminne, Geert; Storme, Veronique et al

in Plant Journal : for Cell & Molecular Biology (2006), 47(2), 224-37

Genetical metabolomics [metabolite profiling combined with quantitative trait locus (QTL) analysis] has been proposed as a new tool to identify loci that control metabolite abundances. This concept was ... [more ▼]

Genetical metabolomics [metabolite profiling combined with quantitative trait locus (QTL) analysis] has been proposed as a new tool to identify loci that control metabolite abundances. This concept was evaluated in a case study with the model tree Populus. Using HPLC, the peak abundances were analyzed of 15 closely related flavonoids present in apical tissues of two full-sib poplar families, Populus deltoides cv. S9-2 x P. nigra cv. Ghoy and P. deltoides cv. S9-2 x P. trichocarpa cv. V24, and correlation and QTL analysis were used to detect flux control points in flavonoid biosynthesis. Four robust metabolite quantitative trait loci (mQTL), associated with rate-limiting steps in flavonoid biosynthesis, were mapped. Each mQTL was involved in the flux control to one or two flavonoids. Based on the identities of the affected metabolites and the flavonoid pathway structure, a tentative function was assigned to three of these mQTL, and the corresponding candidate genes were mapped. The data indicate that the combination of metabolite profiling with QTL analysis is a valuable tool to identify control points in a complex metabolic pathway of closely related compounds. [less ▲]

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See detailGenetically engineered polypeptides as a new tool for inorganic nano-particles separation in water based media
Vreuls, Christelle ULg; Genin, Alexis ULg; Zocchi, Germaine ULg et al

in Journal of Materials Chemistry (2011), 21

The present paper relates a method for the separation of an insoluble inorganic powder out of a mixture of several insoluble powders with different chemical compositions, using genetically engineered ... [more ▼]

The present paper relates a method for the separation of an insoluble inorganic powder out of a mixture of several insoluble powders with different chemical compositions, using genetically engineered inorganic binding peptides (GEPI). GEPI are small peptides that recognize and specifically bind an inorganic solid material. This GEPI is anchored to magnetic beads for easy recovery of the powder of interest from the mixture. [less ▲]

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See detailGenetics and genomics of energy balance measured in milk using mid-infrared spectroscopy
McParland, Sinead; Calus, Mario; Coffey, Mike et al

Poster (2012, August)

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See detailGenetics and genomics of energy balance measured in milk using mid-infrared spectroscopy
McParland, Sinead; Calus, Mario; Coffey, Mike et al

in Book of Abstracts of the 63rd Annual Meeting of the European Federation of Animal Science (2012, August)

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See detailGenetics and Inflammatory Bowel Disease: From Association Studies to Wide Genome Screen
Louis, Edouard ULg; Belaiche, Jacques ULg

in Acta Gastro-Enterologica Belgica (1997), 60(3, Jul-Sep), 201-3

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See detailThe genetics and molecular biology of mitochondria in Chlamydomonas
Matagne, René-Fernand ULg; Remacle, Claire ULg

in Pandalai, S. (Ed.) Recent Research Development in Plant Biology (2002)

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See detailGenetics and regulation of bacterial virulence: towards the molecular version of Koch's postulates
Mainil, Jacques ULg

Conference given outside the academic context (2005)

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See detailThe Genetics in Cushing syndrome
Vandeva, S.; Daly, Adrian ULg; Vroonen, Laurent ULg et al

in European Neuroendocrine Association - Workshop : Novel experimental data on the pituitary and adrenal tumors responsible for Cushing's syndrome (2009)

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See detailThe genetics in Cushing's syndrome
Beckers, Albert ULg

Scientific conference (2009, December)

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See detailGenetics of Crohn's Disease Behaviour
Louis, Edouard ULg; Belaiche, Jacques ULg

in Acta Gastro-Enterologica Belgica (2000), 63(4, Oct-Dec), 377-9

Crohn's disease is probably an heterogeneous entity. This heterogeneity may be linked to either genetics or environment. In particular the behaviour of the disease, i.e. the tendency to develop ... [more ▼]

Crohn's disease is probably an heterogeneous entity. This heterogeneity may be linked to either genetics or environment. In particular the behaviour of the disease, i.e. the tendency to develop stricturing and/or penetrating lesions, may be linked to the genetic background. While epidemiological and clinical data suggest the relevance of these behavioural classifications, the progresses in the characterization of the immuno-inflammatory reaction in the bowel wall shed a new light on possible candidate genes for these genetic predispositions to various Crohn's disease behaviours. Association studies an linkage analysis focusing on growth factors, metalloproteinases and their tissue inhibitors as well as cytokines may bring new interesting data in this field. [less ▲]

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See detailGenetics of Cushing's Syndrome
Yaneva, M.; Vandeva-Kalvacheva, Silvia ULg; Zacharieva, S. et al

in Neuroendocrinology (2010), 92((supp. 1)), 6-10

Cushing's syndrome (CS) is characterized by pathologically elevated free glucocorticoid levels. Endogenous hypercortisolism is usually due to ACTH-secreting pituitary corticotropic adenomas and less often ... [more ▼]

Cushing's syndrome (CS) is characterized by pathologically elevated free glucocorticoid levels. Endogenous hypercortisolism is usually due to ACTH-secreting pituitary corticotropic adenomas and less often due to ectopic ACTH-secreting neuroendocrine neoplasms or ACTH-independent adrenal cortisol hypersecretion. CS is a serious chronic disease leading to a several-fold increase in cardiovascular morbidity and mortality. Multiple genetic alterations have been described in the setting of sporadic corticotropinoma formation. Changes in the expression profiles have been demonstrated in growth factors and their receptors, cell-cycle regulators and in various genes related to hormonal gene transcription, synthesis and secretion. Sporadic adrenal adenomas and carcinomas may demonstrate dysfunction in genes such as TP53 among others. Cushing's disease can be an inherited condition also. Multiple endocrine neoplasia type 1 (MEN1) and familial isolated pituitary adenomas (FIPA) together account for 5% of pituitary adenomas. Cushing's disease occurs infrequently in an inherited setting in both of these conditions. To date only 2 cases of Cushing's disease have been described in association with mutations in AIP. One case of Cushing's disease has been reported as part of MEN4, a rare MEN1-like syndrome due to mutation in the CDKN1B gene. Carney complex (CNC) due to PRKAR1A mutations in most cases is associated with CS, mainly as a cause of bilateral adrenal hyperplasia. The cAMP signaling pathway is affected in this setting. In recent times the involvement of genes such as PDE11A, PDE8B and others have expanded the spectrum of the genetic pathophysiology of CS. [less ▲]

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See detailGenetics of familial pituitary tumors
Beckers, Albert ULg

Scientific conference (2011, December 01)

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See detailThe Genetics of Growth Hormone Axis
Beckers, Albert ULg; Beckers, Albert ULg

Textual, factual or bibliographical database (2003)

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See detailThe Genetics of Growth Hormone Axis
Beckers, Albert ULg; Beckers, Albert ULg

Textual, factual or bibliographical database (2004)

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See detailGenetics of lactation persistency
Swalve, H. H.; Gengler, Nicolas ULg

in British Society of Animal Science Occasional Publication (1999), 24

Lactation persistency, often simply called persistency, in general can be defined as the ability to maintain yields during the lactation. Persistency has an impact on feed costs, health, and fertility. Of ... [more ▼]

Lactation persistency, often simply called persistency, in general can be defined as the ability to maintain yields during the lactation. Persistency has an impact on feed costs, health, and fertility. Of these three components affected by persistency, the impact of persistency on health, i.e. metabolic stress of the cow leading to health problems, may be most important nowadays. Numerous suggestions for criteria of persistency exist. Often simple ratios of part-lactation yields, e.g. the ratio of yield in the first and last 100 days of lactation, have been used. New approaches have used results from the application of random regression test day models developed for the genetic evaluation of yield traits. Many studies have unfortunately neglected the effect of gestation on persistency but acknowledged that an improved persistency should lead to an improved reproductive performance. Both relationships should be considered in genetic analyses and recommendations for improvement of management decisions. Today the correct description of persistency plays a prominent role to obtain correct genetic evaluations based on test day yields. But, although apparently trivial, a direct genetic analysis of lactation persistency and even more an inclusion of this trait into selection programmes clearly is a complicated task. A reason for this, amongst others, is that management strategies for feeding during the lactation and handling of the reproductive performance that are most often not recorded, are likely to mask the real persistency. Future studies on the genetics of persistency should also seek a strong interaction of geneticists and physiologists as persistency is fundamentally confounded with the problem of metabolic stress. Today, a recommendation of the inclusion of persistency in selection programmes appears to be premature and more studies, e. g. on the association of persistency with longevity, could aid in this process. [less ▲]

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See detailGenetics of menopause-associated diseases.
Massart, François ULg; REGINSTER, Jean-Yves ULg; Brandi, M L

in Maturitas (2001), 40(2), 103-16

Menopause is the permanent cessation of menstruation resulting from the loss of ovarian follicular activity. It is estimated that perhaps 50 million women worldwide will go into menopause annually ... [more ▼]

Menopause is the permanent cessation of menstruation resulting from the loss of ovarian follicular activity. It is estimated that perhaps 50 million women worldwide will go into menopause annually. Atherosclerotic cardiovascular disease, osteoporotic fractures and Alzheimer's dementia are common chronic disorders after menopause, representing major health problems in most developed countries. Apart from being influenced by environmental factors, these chronic disorders recognize a strong genetic component, and there are now considerable clinic evidences that these disorders are related to low hormonal milieu of postmenopausal women. Here, we review up-to-date available data suggesting that genetic variation may contribute to higher susceptibility to four sporadic chronic syndromes such as osteoporosis (OP), osteoarthritis (OA), Alzheimer's disease (AD) and coronary artery disease (CAD). For these four syndromes candidate genes that today appear as major loci in genetic susceptibility encode for proteins specific of a given system, as the vitamin D receptor (VDR) gene for the skeleton and, therefore, OP or angiotensin converting enzyme (ACE) for the cardiovascular system and, therefore, CAD. The investigation of gene polymorphisms in various pathological conditions typical of postmenopause offer an explanation not only of their genetic inheritance but also of their co-segregation in given individuals. In this view, it may be possible to identify a common set of genes whose variants contribute to a common genetic background for these different disorders. Ideal candidates appear genes of the estrogen response cascade [i.e. estrogen receptor (ERs), enzymes involved in estrogen metabolism or co-activators and co-inhibitors]. All together this information may represent the basis both for future recognition of individuals at risk and for the pharmacogenetic driving of drug responsiveness. [less ▲]

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See detailGenetics of migraine: Possible links to neurophysiological abnormalities
Sandor, P. S.; Ambrosini, A.; Agosti, R. M. et al

in Headache (2002), 42(5), 365-377

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See detailGenetics of pituitary adenomas
Beckers, Albert ULg

in Médecine Clinique Endocrinologie & Diabète (2012)

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