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See detailGenetics of mastitis in the Walloon Region of Belgium
Bastin, Catherine ULg; Vandenplas, Jérémie ULg; Laine, Aurélie ULg et al

in Book of Abstracts of the 64th Annual Meeting of the European Federation of Animal Science (2013, August)

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See detailGenetics of mastitis in the Walloon Region of Belgium
Bastin, Catherine ULg; Vandenplas, Jérémie ULg; Laine, Aurélie ULg et al

Conference (2013, August)

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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

Scientific conference (2009, May)

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See detailGenetics of pituitary adenomas
Beckers, Albert ULg

in Médecine Clinique Endocrinologie & Diabète (2012)

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See detailGenetics of pituitary adenomas
Beckers, Albert ULg

Scientific conference (2014, March 22)

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See detailThe genetics of pituitary adenomas
Vandeva-Kalvacheva, Silvia ULg; Jaffrain-Rea, M. L.; Daly, Adrian ULg et al

in Best Practice & Research. Clinical Endocrinology & Metabolism (2010), 24(3), 461-76

Pituitary adenomas are one of the most frequent intracranial tumors with a prevalence of clinically-apparent tumors close to 1:1000 of the general population. They are clinically significant beause of ... [more ▼]

Pituitary adenomas are one of the most frequent intracranial tumors with a prevalence of clinically-apparent tumors close to 1:1000 of the general population. They are clinically significant beause of hormone overproduction and/or tumor mass effects in addition to the need for neurosurgery medical therapies and radiotherapy. The majority of pituitary adenomas have a sporadic origin with recognized genetic mutations seldom being found; somatotropinomas are an exception, presenting frequent somatic GNAS mutations. In this and other phenotypes, tumorigenesis could possibly be explained by altered function of genes implicated in cell cycle regulation, growth factors or their receptors, cell-signaling pathways, specific hormonal factors or other molecules with still unclear mechanisms of action. Genetic changes, such as allelic loss or gene amplification, and epigenetic changes, usually by promoter methylation, have been implicated in abnormal gene expression, but alternative mechanisms may be present. Familial cases of pituitary adenomas represent 5% of all pituitary tumors. MEN1 mutations cause multiple endocrine neoplasia type 1 (MEN1), while the Carney complex (CNC) is charcaterized by mutations in the protein kinase A regulatory subunit-1alpha (PRKAR1A) gene or changes in a locus at 2p16. Recently, a MEN1-like conditions, MEN4, was found to be related to mutations in the CDKN1B gene. The clinical entity of familialt isolated pituitary adenomas (FIPA) is characterized by genetic defects in the aryl hydrocarbon receptor interacting protein (AIP) gene in about 15% of all kindreds and 50% of homogenous somatotropinoma families. Identification of familial cases of pituitary adenomas is important as these tumors may be more aggressive than their sporadic counterparts. [less ▲]

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See detailGenetics of pituitary tumor
Beckers, Albert ULg

Scientific conference (2011, June)

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See detailGenetics of the mid-infrared predicted lactoferrin content in milk of dairy cows
Bastin, Catherine ULg; Leclercq, Gil ULg; Soyeurt, Hélène ULg et al

in Book of Astracts of the 63rd Annual Meeting of the European Federation of Animal Science (2012)

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See detailGenetics of the mid-infrared prediction of lactoferrin content in milk for Holstein first-parity cows
Bastin, Catherine ULg; Leclercq, Gil ULg; Soyeurt, Hélène ULg et al

in International Journal of Dairy Science (2012), 95, Suppl. 2

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See detailGenetics of the mineral contents in bovine milk predicted by mid-infrared spectrometry
Soyeurt, Hélène ULg; Dehareng, Frédéric; Romnée, Jean-Michel et al

Conference (2012, August 27)

Knowing the contents of minerals in milk like Ca or Na could be interesting to improve the nutritional quality of milk and to assess the animal health status. This study had two aims: 1) development of ... [more ▼]

Knowing the contents of minerals in milk like Ca or Na could be interesting to improve the nutritional quality of milk and to assess the animal health status. This study had two aims: 1) development of mid-infrared equations for mineral contents in milk by using an approach combining multiple countries, breeds, and production systems and 2) study of the genetic variability of these traits in the Walloon Holstein dairy cattle. Samples included in the calibration set were collected in Belgium, Luxembourg and France over 5 years. The calibration set included at least 400 samples analyzed by coupled plasma atomic emission spectrometry to quantify the contents of Na, Ca, Mg, P and K. The calibration coefficient of determination ranged between 0.69 for K and 0.93 for Na. The standard error of cross-validation was 63.35, 49.24, 64.33, 7.04, and 93.22 mg/kg of milk for Na, Ca, P, Mg and K. From these results, the quantification of milk minerals by mid-infrared is feasible. These equations were applied to more than 140,000 spectral records collected from 43,797 first parity Holstein cows in 1,233 herds. The variance components were estimated using Gibbs Sampling using single trait random regression models derived from the one used for the Walloon genetic evaluation of milk production traits. First results gave a daily heritability of 0.26 for Na, 0.45 for Ca, 0.48 for P, 0.46 for Mg, and 0.41 for K. Moderate negative genetic correlations were found between Na and the other studied traits. The highest correlation (0.69) was observed between P and Mg. These results confirmed the genetic variability of these traits. Further studies will be conducted to study the relationship between these traits and other traits (e.g., production, health). [less ▲]

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See detailGenetics of the mineral contents in bovine milk predicted by mid-infrared spectrometry
Soyeurt, Hélène ULg; Dehareng, Frédéric; Romnée, Jean-Michel et al

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

Knowing the contents of minerals in milk like Ca or Na could be interesting to improve the nutritional quality of milk and to assess the animal health status. This study had two aims: 1) development of ... [more ▼]

Knowing the contents of minerals in milk like Ca or Na could be interesting to improve the nutritional quality of milk and to assess the animal health status. This study had two aims: 1) development of mid-infrared equations for mineral contents in milk by using an approach combining multiple countries, breeds, and production systems and 2) study of the genetic variability of these traits in the Walloon Holstein dairy cattle. Samples included in the calibration set were collected in Belgium, Luxembourg and France over 5 years. The calibration set included at least 400 samples analyzed by coupled plasma atomic emission spectrometry to quantify the contents of Na, Ca, Mg, P and K. The calibration coefficient of determination ranged between 0.69 for K and 0.93 for Na. The standard error of cross-validation was 63.35, 49.24, 64.33, 7.04, and 93.22 mg/kg of milk for Na, Ca, P, Mg and K. From these results, the quantification of milk minerals by mid-infrared is feasible. These equations were applied to more than 140,000 spectral records collected from 43,797 first parity Holstein cows in 1,233 herds. The variance components were estimated using Gibbs Sampling using single trait random regression models derived from the one used for the Walloon genetic evaluation of milk production traits. First results gave a daily heritability of 0.26 for Na, 0.45 for Ca, 0.48 for P, 0.46 for Mg, and 0.41 for K. Moderate negative genetic correlations were found between Na and the other studied traits. The highest correlation (0.69) was observed between P and Mg. These results confirmed the genetic variability of these traits. Further studies will be conducted to study the relationship between these traits and other traits (e.g., production, health). [less ▲]

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See detailGenetics of ulcerative colitis: the come-back of interleukin 10.
Louis, Edouard ULg; Libioulle, Cécile ULg; Reenaers, Catherine ULg et al

in Gut (2009), 58(9), 1173-6

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See detailGénétique de la Néphropathie diabétique
Hadjadj, Samy; Weekers, Laurent ULg; Marre, Michel

in Sang Thrombose Vaisseaux [=STV] (2000), 12(3), 151-156

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See detailGénétique de la neuropathie laryngée récurrente chez le cheval
Dupuis, Marie-Capucine ULg

Doctoral thesis (2011)

Recurrent laryngeal neuropathy (RLN), known as « roaring » or « whistling », has been considered as the most important equine airway disease of the horse. It can cause abnormal respiratory noise during ... [more ▼]

Recurrent laryngeal neuropathy (RLN), known as « roaring » or « whistling », has been considered as the most important equine airway disease of the horse. It can cause abnormal respiratory noise during fast exercise, secondary to a reduced abduction of the left arytenoid cartilage, which may impair performance. Despite significant research into the disease, some aspects, such as etiology and pathogenesis, remain unknown. Several papers suggest a genetic basis but molecular studies have never been reported. Using the EquineSNP50 Beadchip, we genotyped 234 cases (196 Warmbloods, 20 Trotters, 14 Thoroughbreds and 4 Draft Horses), 228 breed-matched controls and 69 parents. Linkage disequilibrium and population structure were quantified before performing single marker and haplotype-based association studies, as well as family-based linkage analyses. Two genome-wide suggestive loci were identified on chromosomes 21 and 31, driven by the enrichment of a “protective” haplotype in controls compared to cases. Our study indicates that predisposition to RLN has a complex determinism, probably involving a high number of genes, of which the candidates on chromosome 21 and 31 may have the largest effects. We performed a copy-number variants analysis on the same data. After characterization of the regions harbouring these variants, an association study with RLN was conducted. A duplication on chromosome 10 was identified in ten affected horses and two unphenotyped parents that were sharing a long haplotype. This work provides novel insights in the genetic determinism of NLR and opens new field of research. If the genuine nature of these loci is confirmed in independent cohorts, identifying the causative genes may increase our understanding of RLN pathogenesis. Assuming that RLN is very polygenic, predictive diagnosis and selection may be more effective using a genomic selection type of approach. [less ▲]

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See detailGénétique des adénomes hypophysaires
Beckers, Albert ULg

Scientific conference (2014, May 23)

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See detailLa génétique des migraines : des canaux ioniques aux polymorphismes de nucléotide ?
FUMAL, Arnaud ULg; Schoenen, Jean ULg

in Revue Médicale de Liège (2004), 59(6), 367-377

Detailed reference viewed: 21 (6 ULg)