16 results on '"Torres I.M."'
Search Results
2. Increased pulsatility index supports diagnosis of vascular parkinsonism versus idiopathic Parkinson's disease
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Caba, L.M., Ferrairó, J.I.T., Torres, I.M., Costa, J.F.V., Muñoz, R.B., and Martin, A.L.
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- 2020
- Full Text
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3. Behavior of total and free serum testosterone as a predictor for the risk of prostate cancer and its aggressiveness
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Regis, L., Planas, J., Celma, A., de Torres, I.M., Ferrer, R., and Morote, J.
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- 2015
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4. Sedentarism and overweight as risk factors for the detection of prostate cancer and its aggressiveness
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Morote, J., Celma, A., Planas, J., Placer, J., Konstantinidis, C., Iztueta, I., de Torres, I.M., Oliván, M., Reventós, J., and Doll, A.
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- 2014
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5. Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage
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Chen, Z., Zhang, D., Reynolds, R.H., Gustavsson, E.K., García-Ruiz, S., D'Sa, K., Fairbrother-Browne, A., Vandrovcova, J., Noyce, A.J., Kaiyrzhanov, R., Middlehurst, B., Kia, D.A., Tan, M., Morris, H.R., Plun-Favreau, H., Holmans, P., Trabzuni, D., Bras, J., Quinn, J., Mok, K.Y., Kinghorn, K.J., Billingsley, K., Wood, N.W., Lewis, P., Schreglmann, S., Guerreiro, Rita, Lovering, R., R'Bibo, L., Manzoni, C., Rizig, M., Guelfi, S., Escott-Price, V., Chelban, V., Foltynie, T., Williams, N., Brice, A., Danjou, F., Lesage, S., Corvol, Jean-Christophe, Martinez, M., Schulte, C., Brockmann, K., Simón-Sánchez, J., Heutink, P., Rizzu, P., Sharma, M., Gasser, T., Nicolas, A., Cookson, M. R, Bandres-Ciga, S., Blauwendraat, Cornelis, Craig, David W, Faghri, F., Gibbs, J.R., Hernandez, D.G., Van Keuren-Jensen, K., Shulman, J.M., Leonard, H.L., Nalls, M.A., Robak, L., Lubbe, S., Finkbeiner, S., Mencacci, N.E., Lungu, C., Singleton, A. B., Scholz, S.W., Reed, X., Alcalay, Roy N, Gan-Or, Z., Rouleau, G.A., Krohn, L., van Hilten, J.J., Marinus, J., Adarmes-Gómez, A.D, Aguilar Barberà, Miquel, Alvarez, Ignacio, Alvarez, V., Barrero, F. J, Yarza, J.A.B., Bernal-Bernal, I., Blazquez, M., Bonilla-Toribio, Marta, Botía, J., Boungiorno, M.T., Buiza-Rueda, Dolores, Cámara, Ana, Carrillo, F., Carrión-Claro, M., Cerdan, D., Clarimón, Jordi, Compta, Yaroslau, Diez-Fairen, M., Dols Icardo, Oriol, Duarte, J., Duran, Raquel, Escamilla-Sevilla, F., Ezquerra, M., Feliz, C., Fernández, M., Fernández-Santiago, R., Garcia, C., García-Ruiz, P., Gómez-Garre, P., Heredia, M.J.G., Gonzalez-Aramburu, I., Pagola, A.G., Hoenicka, J., Infante, J., Jesús, S., Jimenez-Escrig, A., Kulisevsky, Jaime, Labrador-Espinosa, Miguel A, Lopez-Sendon, J.L., de Munain Arregui, A.L., Macias, D., Torres, I.M., Marín, J., Marti, M.J., Martínez-Castrillo, J.C., Méndez-del-Barrio, C., González, M.M., Mata, M., Mínguez, A., Mir, P., Rezola, E.M., Muñoz, E., Pagonabarraga Mora, Javier, Pastor, P., Errazquin, F.P., Periñán-Tocino, T., Ruiz-Martínez, J., Ruz, C., Rodriguez, A.S., Sierra, M., Suarez-Sanmartin, E., Tabernero, C., Tartari, J. P., Tejera-Parrado, C., Tolosa, E., Valldeoriola, F., Vargas-González, L., Vela, L., Vives, F., Zimprich, Alexander, Pihlstrom, L., Toft, M., Koks, S., Taba, P., Hassin-Baer, S., Hardy, J., Houlden, Henry, Gagliano Taliun, S. A., Ryten, M., Universitat Autònoma de Barcelona, Universidad de Cantabria, Lord Leonard and Lady Estelle Wolfson Foundation, Medical Research Council (UK), Dementia Research Institute (UK), Alzheimer Society, Alzheimer's Research UK, Wellcome Trust, Dolby Family Fund, National Institute for Health Research (UK), NIHR Biomedical Research Centre (UK), Agencia Estatal de Investigación (España), Fundación Séneca, and Gobierno de la Región de Murcia
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0301 basic medicine ,Apolipoprotein E ,Aging ,Messenger ,General Physics and Astronomy ,Neurodegenerative ,Alzheimer's Disease ,Genome ,Linkage Disequilibrium ,Negative selection ,0302 clinical medicine ,2.1 Biological and endogenous factors ,Aetiology ,health care economics and organizations ,Conserved Sequence ,Phylogeny ,Multidisciplinary ,Brain ,Neurodegenerative Diseases ,Single Nucleotide ,Alzheimer's disease ,Phenotype ,International Parkinson’s Disease Genomics Consortium ,Neurological ,Regression Analysis ,Long Noncoding ,DNA, Intergenic ,RNA, Long Noncoding ,Human ,Biotechnology ,Lineage (genetic) ,Science ,1.1 Normal biological development and functioning ,Computational biology ,Biology ,Polymorphism, Single Nucleotide ,Article ,General Biochemistry, Genetics and Molecular Biology ,Chromosomes ,03 medical and health sciences ,Apolipoproteins E ,Underpinning research ,Alzheimer Disease ,Genetic variation ,Genetics ,Acquired Cognitive Impairment ,Humans ,RNA, Messenger ,Polymorphism ,Gene ,Whole genome sequencing ,Intergenic ,Pair 19 ,Genome, Human ,Human Genome ,Neurosciences ,Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD) ,Molecular Sequence Annotation ,General Chemistry ,DNA ,Introns ,Brain Disorders ,030104 developmental biology ,Gene Ontology ,RNA ,Dementia ,Chromosomes, Human, Pair 19 ,030217 neurology & neurosurgery - Abstract
Knowledge of genomic features specific to the human lineage may provide insights into brain-related diseases. We leverage high-depth whole genome sequencing data to generate a combined annotation identifying regions simultaneously depleted for genetic variation (constrained regions) and poorly conserved across primates. We propose that these constrained, non-conserved regions (CNCRs) have been subject to human-specific purifying selection and are enriched for brain-specific elements. We find that CNCRs are depleted from protein-coding genes but enriched within lncRNAs. We demonstrate that per-SNP heritability of a range of brain-relevant phenotypes are enriched within CNCRs. We find that genes implicated in neurological diseases have high CNCR density, including APOE, highlighting an unannotated intron-3 retention event. Using human brain RNA-sequencing data, we show the intron-3-retaining transcript to be more abundant in Alzheimer’s disease with more severe tau and amyloid pathological burden. Thus, we demonstrate potential association of human-lineage-specific sequences in brain development and neurological disease., Knowledge of genomic features specific to humans may be important for understanding disease. Here the authors demonstrate a potential role for these human-lineage-specific sequences in brain development and neurological disease.
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- 2021
6. Latitude gradient influences the age of onset of rheumatoid arthritis
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Group, G.-R., Ramos-Remus, C., Ramirez-Gomez, A., Brambila-Barba, V., Barajas-Ochoa, A., Castillo-Ortiz, J.D., Adebajo, A.O., Espinoza, L.R., Aceves-Avila, F.J., Sanchez-Gonzalez, J.M., Boudersa, N., Slimani, S., Ladjouze-Rezig, A., Diaz, M.P., Kirmayr, K.I., Asnal, C.A., Catoggio, L.J., Citera, G., Casado, G.C., Alvarez, A.P., Pisoni, C.N., Benavente, E. Diez, Lopez-Cabanillas, A., Baez, R.M., Pons-Estel, B.A., Sacnun, M.P., Cavallasca, J.A., Paniego, R.H., Proudman, S.M., Thomas, R., Major, G., Mathers, D.M., Schrieber, L., Haq, S.A., Islam, N., Dessein, P.H., Muhlen, C.A. Von, Bianchi, W.A., Castelar-Pinheiro, G. da Rocha, Feldman-Pollak, D., Cossermelli, W., Bonfiglioli, K.R., Giorgi, R.D., Zabsonre-Tiendrebeogo, W.J., Russell, A.S., Olaru, L., Karsh, J., Fuentealba, C., Aguilera, S., Castro-Esparza, I.H., Burgos, P.I., Neira, O., Li, Z.-G., Tam, L.-S., Mok, M.Y., Medina, Y.F., Moreno-Alvarez, M.J., Zuniga-Vera, A.E., Vera, C., Quezada, I., Moreno, I.M., Calapaqui, W., El-Mardenly, G., Salama, M.S., Ragab, G., Hadidi, T., Gado, K., Leirisalo-Repo, M., Tuompo, R., Koivuniemi, R., Berenbaum, F., Allanore, Y., Constantin, A., Buttgereit, F., Schulze-Koops, H., Liz, M., Dey, D., Alonzo-Borjas, H.D., Santiago-Pastelin, C.B., Cuellar-Cruz, V., Dharmanand, B.G., Yathish, G.C., Akerkar, S.M., Malaviya, A.N., Ahmadzadeh, A., Hasunuma, T., Owino, B.O., Pacheco-Tena, C., Frausto-Arenas, A., Madrid-Cernas, A.A. De la, Cardona-Cabrera, R., Centeno-Valadez, J.D., Rodriguez-Torres, I.M., Vaidya, B., Gupta, A.K., Harrison, A.A., Grainger, R., Nwankwo, H.M., Diamantopoulos, A.P., Maland, E., et al., Jansen, T.L., Riel, P. van, Nunez-Sotelo, C.M., Villegas-Morales, S., Rheumatology, AII - Inflammatory diseases, Experimental Immunology, Clinical Immunology and Rheumatology, Clinicum, University of Helsinki, Reumatologian yksikkö, and HUS Internal Medicine and Rehabilitation
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Male ,rheumatoid arthritis ,Multivariate analysis ,inequality ,Cross-sectional study ,Severity of Illness Index ,DISEASE ,Arthritis, Rheumatoid ,0302 clinical medicine ,Surveys and Questionnaires ,Epidemiology ,EPIDEMIOLOGY ,030212 general & internal medicine ,Age of Onset ,RISK ,Medicine(all) ,General Medicine ,ASSOCIATION ,Middle Aged ,Prognosis ,Pollution ,PREVALENCE ,Rheumatoid arthritis ,Cohort ,Disease Progression ,Female ,HEALTH ,Adult ,medicine.medical_specialty ,UNITED-STATES ,Tropic of Cancer ,Healthcare improvement science Radboud Institute for Health Sciences [Radboudumc 18] ,Environmental ,03 medical and health sciences ,Rheumatology ,Severity of illness ,medicine ,Humans ,COHORT ,METAANALYSIS ,030203 arthritis & rheumatology ,Geoepidemiology ,business.industry ,AIR-POLLUTION ,medicine.disease ,Cross-Sectional Studies ,3121 General medicine, internal medicine and other clinical medicine ,Physical therapy ,Age of onset ,business ,Demography - Abstract
The age of onset of rheumatoid arthritis (RA) is an important outcome predictor. Northern countries report an age of RA onset of around 50 years, but apparently, variability exists across different geographical regions. The objective of the present study is to assess whether the age of onset of RA varies across latitudes worldwide. In a proof-of-concept cross-sectional worldwide survey, rheumatologists from preselected cities interviewed 20 consecutive RA patients regarding the date of RA onset (RAO, when the patient first noted a swollen joint). Other studied variables included location of each city, rheumatologist settings, latitudes (10° increments, south to north), longitudes (three regions), intracountry consistency, and countries’ Inequality-adjusted Human Development Index (IHDI). Data from 2481 patients (82% females) were obtained from 126 rheumatologists in 77 cities of 41 countries. Worldwide mean age of RAO was 44 ± 14 years (95% CI 44–45). In 28% of patients, RA began before age 36 years and before age 46 years in 50% of patients. RAO was 8 years earlier around the Tropic of Cancer when compared with northern latitudes (p 2 0.045, p 2 0.5). RA often begins at an early age and onset varies across latitudes worldwide. We postulate that countries’ developmental status and their geographical and geomagnetic location influence the age of RAO.
- Published
- 2017
7. Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson's disease heritability
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Reynolds, R.H., Botia, J., Nalls, M.A., Hardy, J., Taliun, S.A.G., Ryten, M., Noyce, A.J., Nicolas, A., Cookson, M.R., Bandres-Ciga, S., Gibbs, J.R., Hernandez, D.G., Singleton, A.B., Reed, X., Leonard, H., Blauwendraat, C., Faghri, F., Bras, J., Guerreiro, R., Tucci, A., Kia, D.A., Houlden, H., Plun-Favreau, H., Mok, K.Y., Wood, N.W., Lovering, R., R'Bibo, L., Rizig, M., Chelban, V., Trabzuni, D., Tan, M., Morris, H.R., Middlehurst, B., Quinn, J., Billingsley, K., Holmans, P., Kinghorn, K.J., Lewis, P., Escott-Price, V., Williams, N., Foltynie, T., Brice, A., Danjou, F., Lesage, S., Corvol, J.C., Martinez, M., Giri, A., Schulte, C., Brockmann, K., Simon-Sanchez, J., Heutink, P., Gasser, T., Rizzu, P., Sharma, M., Shulman, J.M., Robak, L., Lubbe, S., Mencacci, N.E., Finkbeiner, S., Lungu, C., Scholz, S.W., Gan-Or, Z., Rouleau, G.A., Krohan, L., Hilten, J.J. van, Marinus, J., Adarmes-Gomez, A.D., Bernal-Bernal, I., Bonilla-Toribio, M., Buiza-Rueda, D., Carrillo, F., Carrion-Claro, M., Mir, P., Gomez-Garre, P., Jesus, S., Labrador-Espinosa, M.A., Macias, D., Vargas-Gonzalez, L., Mendez-del-Barrio, C., Perinan-Tocino, T., Tejera-Parrado, C., Diez-Fairen, M., Aguilar, M., Alvarez, I., Boungiorno, M.T., Carcel, M., Pastor, P., Tartari, J.P., Alvarez, V., Gonzalez, M.M., Blazquez, M., Garcia, C., Suarez-Sanmartin, E., Barrero, F.J., Rezola, E.M., Yarza, J.A.B., Pagola, A.G., Arregui, A.L.D., Ruiz-Martinez, J., Cerdan, D., Duarte, J., Clarimon, J., Dols-Icardo, O., Infante, J., Marin, J., Kulisevsky, J., Pagonabarraga, J., Gonzalez-Aramburu, I., Rodriguez, A.S., Sierra, M., Duran, R., Ruz, C., Vives, F., Escamilla-Sevilla, F., Minguez, A., Camara, A., Compta, Y., Ezquerra, M., Marti, M.J., Fernandez, M., Munoz, E., Fernandez-Santiago, R., Tolosa, E., Valldeoriola, F., Garcia-Ruiz, P., Heredia, M.J.G., Errazquin, F.P., Hoenicka, J., Jimenez-Escrig, A., Martinez-Castrillo, J.C., Lopez-Sendon, J.L., Torres, I.M., Tabernero, C., Vela, L., Zimprich, A., Pihlstrom, L., Koks, S., Taba, P., Majamaa, K., Siitonen, A., Okubadejo, N.U., Ojo, O.O., Pitcher, T., Anderson, T., Bentley, S., Fowdar, J., Mellick, G., Dalrymple-Alford, J., Henders, A.K., Kassam, I., Montgomery, G., Sidorenko, J., Zhang, F.T., Xue, A.L., Vallerga, C.L., Wallace, L., Wray, N.R., Yang, J., Visscher, P.M., Gratten, J., Silburn, P.A., Halliday, G., Hickie, I., Kwok, J., Lewis, S., Kennedy, M., Pearson, J., Int Parkinsons Dis Genomics, and Syst Genomics Parkinsons Dis
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- 2019
8. PT156 - Who benefits from multiparametric magnetic resonance imaging after the suspicion of prostate cancer?
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Cuadras Sole, M., Celma, A., Regis, L., Salazar, A., Miret, E., Roche, S., De Torres, I.M., Mast, R., Semidey, M.E., Planas, J., and Morote, J.
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- 2019
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9. 1407P - Change of natural history of hereditary diffuse gastric cancer after identification of a novel CDH1 mutation
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Stjepanovic, N., Castro, S., Gadea, N., Carrasco, E., Codina, M., Lopez, A., Semidey, M.E., De Torres, I.M., Alsina, M., Urioste, M., Pena, L., Mercadillo, F., Landolfi, S., and Balmana, J.
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- 2017
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10. 848 Differential gene expression profiling in proliferative inflammatory atrophia compared to prostate carcinoma and high grade prostatic intraneoplasia using frozen microdissected tissues
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Quiles, M.T., Arbós, M.A., De Torres, I.M., Blázquez, C., Reventós, J., and Morote, J.
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- 2012
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11. 347 Early versus late serum testosterone and related hormone profile after radical prostatectomy
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Celma, A., Bastaros, J.M., Delgado, G.M., Agreda, F., Planas, J., Raventos, C.X., Placer, J., De, Torres I.M., Carles, J., and Morote, J.
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- 2012
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12. 87 ROLE OF GENDER AND KIM-1 PROTEIN EXPRESSION IN PORCINE AUTO-TRANSPLANTED GRAFT RECOVERY AFTER LAPAROSCOPIC NEPHRECTOMY
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Celma, A., Raventos Busquets, C.X., Meseguer, A., López-Hellm, J., Riera, M., De Torres, I.M., Bestard, J.E., Mir, C., and Morote, J.
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- 2009
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13. 4. Sleep disorders and objective school performance
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Carvalho, L.B.C., Prado, L.B.F., Ferreira, V.R., Camargo, E.P., Ruotulo, F., Torres, I.M., Potasz, C., Biscuola, F.N., Juliano, M.L., and Prado, G.F.
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- 2009
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14. Effect of flaxseed oil, animal fat, and vitamin E supplementation on growth performance, serum metabolites, and carcass characteristics of finisher pigs, and physical characteristics of pork.
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Huang, C., Chiba, L.I., Magee, W.E., Wang, Y., Griffing, D.A., Torres, I.M., Rodning, S.P., Bratcher, C.L., Bergen, W.G., and Spangler, E.A.
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LINSEED oil , *FAT , *VITAMIN E , *LIPID synthesis , *SERUM - Abstract
Highlights • Dietary supplementation with lipids, such as flaxseed oil, can reduce lipogenesis in pigs and increase intramuscular fat content of pork simultaneously. • Oxidative problems in pork because of dietary inclusion of flaxseed oil can be alleviated by vitamin E supplementation. • Supplementation with 1% flaxseed oil + 1 to 5% poultry fat seemed to have no clear effects on carcass fat or IMF. • Supplementation with 220 IU vitamin E/kg increased carcass lean with 6% lipids, but had no clear effects on other criteria. Abstract Dietary lipid supplementation can reduce de novo lipogenesis and increase intramuscular fat content of pork simultaneously, and vitamin E supplementation can increase the oxidative stability of pork. A total of 96 pigs (Yorkshire) were used to investigate the effect of dietary lipid (0 or 1% flaxseed oil + 1, 3, or 5% poultry fat for diets supplemented with lipids) and vitamin E (11 or 220 IU/kg) supplementation in a 4 × 2 factorial arrangement of treatments on growth performance, serum metabolites, and carcass traits of finisher pigs, and physical characteristics of pork. Forty-eight pens containing 2 gilts or 2 castrated males per pen were randomly assigned to 8 diets with 3 gilt pens and 3 castrated male pens per treatment. Pigs were switched from finisher-1 [initial body weight (BW): 54.3 ± 3.4 kg] to finisher-2 diets when the average pen BW reached 84.1 ± 4.0 kg. Standardized ileal digestible Lys and Ca and P were adjusted with the DE content accordingly to maintain constant Lys, Ca, and P to DE ratios. Pigs were harvested when they reached the target BW of 110.0 ± 3.0 kg. There were no lipid x vitamin E interactions in growth performance. As dietary lipids increased from 0 to 6%, average daily feed intake decreased linearly (P < 0.018) and gain to feed ratio improved linearly (P < 0.001) during the finisher-1, finisher-2, and overall phases. Supplementation with 220 IU vitamin E/kg reduced the efficiency of feed, Lys, and DE utilization for BW gain (P < 0.036) during the finisher-1 and overall phases. As dietary lipids increased, serum cholesterol and triglyceride concentrations increased linearly (P < 0.003). Supplementation of the diet with 1% flaxseed oil + 1, 3, or 5% poultry fat resulted in greater serum total protein, albumin, cholesterol, and triglyceride concentrations (P < 0.037) compared with no lipid supplementation. Pigs fed the diets containing 0, 2, and 4% lipids and supplemented with 220 IU vitamin E/kg had greater 10th rib BF and lower fat-free lean than those fed the dies contained 11 IU vitamin E/kg, whereas 10th rib BF was lower and fat-free lean was greater in pigs those fed the diet containing 6% lipids and supplemented with 200 IU vitamin E/kg than those fed the diet contained 11 IU vitamin E/kg (lipid x vitamin E, P < 0.020). Dietary lipids had no effect on subjective marbling score and ether extract content of loin muscle or most other pork and loin muscle characteristics, but belly thickness and width increased (linear, P < 0.040) as dietary lipids increased. Vitamin E supplementation increased marbling score (P = 0.042), but it had no clear effect on loin muscle color (subjective, and L*, a*, and b*), ham and loin muscle pH, loin muscle characteristics, or belly firmness. As expected, feed intake decreased and feed efficiency improved progressively with increasing dietary lipid supplementation from 0 to 6%. Although there were interactions, dietary lipids seemed to have no clear effects on the carcass BF or fat-free lean. Similarly, dietary supplementation with 1% flaxseed oil + 1, 3, or 5% poultry fat had no effect on subjective marbling score or ether extract content of loin muscle. Supplementation with 220 IU vitamin E/kg increased carcass leanness with 6% dietary lipids, but increased carcass BF with 0 to 4% dietary lipids. Vitamin E supplementation increased subjective marbling score, but seemed to have no clear effects on loin muscle color, ham and loin muscle pH, loin muscle characteristics, or pork belly firmness. [ABSTRACT FROM AUTHOR]
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- 2019
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15. Effect of diet complexity, multi-enzyme complexes, essential oils, and benzoic acid on weanling pigs.
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Wang, Y., Chiba, L.I., Huang, C., Torres, I.M., Wang, L., and Welles, E.G.
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SWINE nutrition , *ANIMAL weaning , *ESSENTIAL oils , *BENZOIC acid , *GUT microbiome - Abstract
The study was conducted to investigate the effect of supplementing a simple corn-soybean meal (SBM) diet with multi-enzyme complexes, essential oils, and benzoic acid on growth performance, serum metabolite profile, serum cytokines, and intestinal microbiota in weanling pigs. Forty-eight gilts and 48 castrated males weaned at 3 to 4 wk of age (initial body weight, 7.96 ± 0.89 kg) were randomly assigned to 4 dietary treatments with 3 gilt and 3 castrated male pens per treatment and 4 gilts or 4 castrated males per pen. A complex diet containing palatable and digestible ingredients was formulated (1.30 g standardized ileal digestible Lys/kg) to serve as the positive control (POS) diet. A simple corn-SBM, negative control (NEG) diet was formulated to be isolysinic to the POS diet, and the NEG diet was supplemented with multi-enzyme complexes (ENZ) or multi-enzyme complexes, essential oils, and benzoic acid (ALL). All diets were formulated to meet or exceed the 2012 NRC nutrient requirements of pigs weighing 7 to 25 kg. During the fourth week, blood samples were collected to determine serum metabolite profile and cytokines, and fecal samples were collected for the enumeration of bacteria. Pigs had ad libitum access to feed and water throughout the 4-wk study. From d 0 to 7 and 7 to 14, pigs fed the POS diet had greater feed and Lys intake ( P < 0.05) and weight gain ( P < 0.05) than those fed the NEG and ALL diets, but there were no differences in those response criteria between pigs fed the POS and ENZ diets. Weight gain of pigs fed the ENZ diet was 17% greater than those fed the NEG diet during the second week ( P < 0.05), but it increased only numerically (16%) during the first week. Overall (d 0 to 28), pigs fed the POS diet consumed more feed, Lys, and digestible energy (DE; P < 0.05) and had greater weight gain ( P < 0.05) than those fed the other diets. Dietary treatments had no effect on the efficiency of feed, Lys, or DE utilization for weight gain during the study. Serum total protein in pigs fed the ENZ and ALL diets was greater ( P < 0.05) than those fed the POS and NEG diets. Pigs fed the ENZ diet had greater serum albumin ( P < 0.05) than those fed the NEG diet. Serum globulin and urea N were lower ( P < 0.05) and albumin to globulin ratio, glucose, and cholesterol were greater ( P < 0.05) in pigs fed the POS diet than those fed the other diets. Dietary treatments had no clear effect on serum cytokines or fecal microbiota. Pigs fed the POS diet grew faster and had lower serum urea N and globulin and greater serum glucose and cholesterol than those fed the other diets. Although supplementation of the NEG diet with multi-enzyme complexes seemed to have beneficial effect on growth performance during the first 2 wk of the study, supplementation of the NEG diet with various feed additives had no clear effects. Further research is needed to explore further the possibility of using a simple corn-SBM diet for weanling pigs by supplementation with multi-enzyme complexes, essential oils, and benzoic acid. [ABSTRACT FROM AUTHOR]
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- 2018
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16. 630 DIFFERENTIAL CHEMOKINE EXPRESSION PROFILE IN PROSTATE CANCER-ASSOCIATED FIBROBLASTS
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Quiles, M.T., Arbós, M.A., De Torres, I.M., Reventós, J., and Morote, J.
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- 2011
- Full Text
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