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المؤلفون: Tsampalieros, A., Berkenstock, M. K., Zemel, B. S., Griffin, L., Shults, J., Burnham, J. M., Baldassano, R. N., Leonard, M. B.

المصدر: Osteoporosis International: With other metabolic bone diseases. July 2014 25(7):1875-1883

المؤلفون: Cardinale, C J, Wei, Z, Panossian, S, Wang, F, Kim, C E, Mentch, F D, Chiavacci, R M, Kachelries, K E, Pandey, R, Grant, S F A^{Aff1, Aff2}, Baldassano, R N^{Aff3, Aff4}, Hakonarson, H^{Aff1, Aff4, IDgene201343_cor12}

المصدر: Genes & Immunity. 14(7):447-452

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المؤلفون: Beaudoin, Melissa, Goyette, Philippe, Goel, Gautam, Louis, E., Mansfield, J. C., Mathew, C. G., McGovern, D. P., Mitrovic, M., Montgomery, G. W., Mowat, C., Newman, W., Palmieri, O., Panés, J., Lagace, Caroline, Parkes, M., Phillips, A., Ponsioen, C. Y., Potocnik, U., Prescott, N. J., Proctor, D. D., Radford-Smith, G. L., Regueiro, M., Rioux, J. D., Roberts, R., Annese, Vito, Rotter, J. I., Rutgeerts, P., Sanderson, J., Sans, M., Satsangi, J., Schreiber, S., Schumm, P., Seibold, F., Sharma, Y., Silverberg, M. S., Bitton, Alain, Simms, L. A., Steinhart, A., Targan, S. R., Taylor, K. D., Torkvist, L., Vermeire, S., Halfvarson, J., Verspaget, H. W., De Vos, M., Walters, T., Begun, Jakob, Wang, K., Weersma, R. K., Whiteman, D., Wijmenga, C., Brant, Steven R., Bresso, Francesca, Cho, Judy H., Duerr, Richard H., Halfvarson, Jonas, Boucher, Gabrielle, McGovern, Dermot P. B., Radford-Smith, Graham, Schreiber, Stefan, Schumm, Philip L., Sharma, Yashoda, Silverberg, Mark S., Weersma, Rinse K., Quebec IBD Genetics Consortium, NIDDK IBD Genetics Consortium, International IBD Genetics Consortium (IIBDGC), Lo, Ken Sin, D'Amato, Mauro, Vermeire, Severine, Franke, Andre, Lettre, Guillaume, Xavier, Ramnik J., Daly, Mark J., Rioux, John D., Aumais, G., Bernard, E. J., Bitton, A., Rivas, Manuel A., Cohen, A., Deslandres, C., Lahaie, R., Paré, P., Brant, S. R., Cho, J. H., Duerr, R. H., Stevens, Christine, Ahmad, T., Anderson, C. A., Annese, V., Baldassano, R. N., Balschun, T., Barclay, M., Barrett, J. C., Bayless, T. M., Bis, J. C., Alikashani, Azadeh, Brand, S., Bumpstead, S., Buning, C., Colombel, J. F., Cottone, M., D'Amato, M., D'Inca, R., Ladouceur, Martin, Daly, M. J., Denson, T., Dubinsky, M., Edwards, C., Ellinghaus, D., Florin, T., Franchimont, D., Franke, A., Gearry, R., Ellinghaus, David, Georges, M., Glas, J., Van Gossum, A., Griffiths, A. M., Guthery, S. L., Hakonarson, H., Haritunians, T., Hugot, J. P., de Jong, D. J., Jostins, L., Torkvist, Leif, Kugathasan, S., Kullak-Ublick, G., Latiano, A., Laukens, D., Lawrance, I., Lee, J., Lees, C. W., Lemann, M., Levine, A., Libioulle, C.

المساهمون: Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI)

المصدر: Plos Genetics, 9, 9, pp. e1003723
PLoS genetics, 9(9):e1003723. PUBLIC LIBRARY SCIENCE
PLoS Genetics, Vol 9, Iss 9, p e1003723 (2013)
PLoS Genetics
PLoS Genetics, 9(9)
Plos Genetics, 9, e1003723
PLOS genetics, 9 (9
Lees, C & Satsangi, J 2013, ' Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis ', PLoS Genetics, vol. 9, no. 9, pp. e1003723 . https://doi.org/10.1371/journal.pgen.1003723
PLoS genetics 9(9), e1003723 (2013). doi:10.1371/journal.pgen.1003723
PLOS GENETICS

مصطلحات موضوعية: Cancer Research, Génétique clinique, LIVER, Genome-wide association study, Inflammatory bowel disease, 0302 clinical medicine, Crohn Disease, GENETIC-VARIANTS, Medicine and Health Sciences, Ethnicity, UBIQUITIN LIGASES, Genetics(clinical), Genetics (clinical), Genetics, 0303 health sciences, Ecology, High-Throughput Nucleotide Sequencing, CROHN-DISEASE, CROHNS-DISEASE, 3. Good health, 030220 oncology & carcinogenesis, Medical genetics, Biologie, Research Article, EXPRESSION, medicine.medical_specialty, Canada, lcsh:QH426-470, SUSCEPTIBILITY LOCI, Evolution, Ubiquitin-Protein Ligases, Ethnic Groups, Evolution des espèces, Biology, Molecular gastro-enterology and hepatology Pathogenesis and modulation of inflammation [IGMD 2], Polymorphism, Single Nucleotide, 03 medical and health sciences, Behavior and Systematics, medicine, Humans, Genetic Predisposition to Disease, Ligase activity, MODULATION, Allele, GENOME-WIDE ASSOCIATION, Molecular Biology, Genotyping, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Genetic association, Ecologie, Biologie moléculaire, Receptors, Interleukin, medicine.disease, NUCLEAR FACTOR 4-ALPHA, Genetic architecture, Cancérologie, CARD Signaling Adaptor Proteins, lcsh:Genetics, CELLS, Colitis, Ulcerative, INTESTINAL EPITHELIAL-CELLS, Genome-Wide Association Study, INFLAMMATORY-BOWEL-DISEASE

وصف الملف: application/pdf; 1 full-text file(s): application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2848aa5d583f624e11893cb2f15d02f6
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/125308

المؤلفون: Cavanaugh, J. A., Bryce, M. E., Stanford, P. M., Pavli, P., Vermeire, S., Peeters, M., Vlietinck, R., Rutgeerts, P., Rioux, J. D., Silverberg, M. S., Steinhart, A. H., Siminovitch, K. A., Hugot, J. P., Lesage, S., Zouali, H., Paavola, P., Halme, L., Färkkilä, M., Kontula, K., Annese, V., Forabosco, P., Fortina, P., Latiano, A., Van Heel, D., Parkes, M., Lench, N., Jewell, D., Brant, S. R., Bailey-Wilson, J. E., Panhuysen, C. I. M., Bayless, T. M., Cho, J. H., Bonen, D. K., Kirschner, B. S., Hanauer, S. B., Yang, H., Taylor, K., Targan, S. R., Rotter, J. I., Silver, J., Gulwani-Akolkar, B., Akolkar, P., Lin, X. -Y., Duerr, R. H., Zhang, L., Achkar, J. P., Baldassano, R. N., Daly, M. J., Risch, N.

مصطلحات موضوعية: Male, Genetic Linkage, International Cooperation, Ulcerative, 0302 clinical medicine, Chromosome Mapping, Chromosomes, Human, Pair 12, Chromosomes, Human, Pair 16, Colitis, Ulcerative, Crohn Disease, European Continental Ancestry Group, Family Characteristics, Female, Genetic Heterogeneity, Genetic Markers, Genetic Predisposition to Disease, Genotype, Humans, Jews, Lod Score, Microsatellite Repeats, Models, Genetic, Nuclear Family, Reproducibility of Results, Statistics, Nonparametric, Genetics, Genetics (clinical), Models, Pair 12, Genetics(clinical), 0303 health sciences, Statistics, Articles, Colitis, 3. Good health, symbols, Microsatellite, 030211 gastroenterology & hepatology, Human, Locus (genetics), Biology, White People, Chromosomes, 03 medical and health sciences, symbols.namesake, Chromosome 16, Genetic, Genetic linkage, Nonparametric, Genotyping, Chromosome 12, 030304 developmental biology, Genetic heterogeneity, Pair 16, Mendelian inheritance

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81fec3e3e0d132bc8783af5f4e9645af
http://hdl.handle.net/11573/1182672

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