المؤلفون: Kauppi, P, Lindblad-Toh, K, Sevon, P, Toivonen, H T T, Rioux, J D, Villapakkam, A, Laitinen, L A, Hudson, T J, Kere, J, Laitinen, T

المساهمون: Department of Mathematics and Statistics, Department of Computer Science, Department of Medical and Clinical Genetics, Finnish Genome Center (-2009), Keuhkosairauksien yksikkö

مصطلحات موضوعية: asthma, atopy, haplotype pattern mining, polymorphism, association, SERUM IGE LEVELS, ALPHA-GENE, LINKAGE DISEQUILIBRIUM, SIGNAL-TRANSDUCTION, POLYMORPHISMS, SUSCEPTIBILITY, CHROMOSOME-5, JAPANESE, MARKERS, 311 Basic medicine

وصف الملف: application/pdf

العلاقة: Kauppi , P , Lindblad-Toh , K , Sevon , P , Toivonen , H T T , Rioux , J D , Villapakkam , A , Laitinen , L A , Hudson , T J , Kere , J & Laitinen , T 2001 , ' Second-generation association study of the 5q31 cytokine gene cluster and the interleukin-4 receptor in asthma ' , Genomics , vol. 2001 , no. 77 , pp. 35-42 .; ORCID: /0000-0003-1339-8022/work/29478278; 0164cd0d-41e1-42b5-a05e-26edb843dac9; http://hdl.handle.net/10138/144008Test; 000170806800007

الإتاحة: http://hdl.handle.net/10138/144008Test

المؤلفون: Villani, Alexandra-Chloé, Lemire, Mathieu, Fortin, Geneviève, Louis, Edouard, Silverberg, M S, Collette, Catherine, Baba, Nobuyasu, Libioulle, C, Belaiche, Jacques, Bitton, A, Gaudet, Daniel, Cohen, Albert, Langelier, D, Fortin, Paul R, Wither, Joan E, Sarfati, Marika, Rutgeerts, Paul, Rioux, J D, Vermeire, Séverine, Hudson, T J, Franchimont, Denis

المصدر: Nature genetics, 41 (1

مصطلحات موضوعية: Sciences bio-médicales et agricoles, Base Pairing, Carrier Proteins -- genetics, Carrier Proteins -- metabolism, Case-Control Studies, Crohn Disease -- genetics, Gene Expression Regulation, Genetic Predisposition to Disease, Humans, Polymorphism, Single Nucleotide -- genetics, Reproducibility of Results

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

العلاقة: uri/info:doi/10.1038/ng.285; uri/info:pii/ng.285; uri/info:pmid/19098911; uri/info:scp/58149159542; uri/info:pmcid/PMC2728932; https://dipot.ulb.ac.be/dspace/bitstream/2013/54794/4/PMC2728932.pdfTest; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/54794Test

الإتاحة: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/54794Test
https://dipot.ulb.ac.be/dspace/bitstream/2013/54794/4/PMC2728932.pdfTest

المؤلفون: Zwarts, K. Y., Clee, S. M., Zwinderman, A. H., Engert, J. C., Singaraja, R., Loubser, O., James, E., Roomp, Kirsten, Hudson, T. J., Jukema, J. W., Kastelein, J. J., Hayden, M. R.

المصدر: Clinical Genetics, 61 (2), 115-125 (2002)

مصطلحات موضوعية: 5' Untranslated Regions, Random Allocation, Promoter Regions, Genetic, Polymorphism, Single Nucleotide, Restriction Fragment Length, Phenotype, Mutation, Models, Male, Lipids/ blood, Humans, Gene Expression Regulation, Coronary Artery Disease/ genetics, Cohort Studies, ATP-Binding Cassette Transporters/ genetics, Time Factors, Life sciences, Sciences du vivant

العلاقة: urn:issn:1399-0004; https://orbilu.uni.lu/handle/10993/27008Test; info:hdl:10993/27008; scopus-id:2-s2.0-0036488074; info:pmid:11940086; wos:000174843700008

الإتاحة: https://doi.org/10.1034Test/j.1399-0004.2002.610206.x
https://orbilu.uni.lu/handle/10993/27008Test

المؤلفون: Clee, S. M., Zwinderman, A. H., Engert, J. C., Zwarts, K. Y., Molhuizen, H. O., Roomp, Kirsten, Jukema, J. W., van Wijland, M., van Dam, M., Hudson, T. J., Brooks-Wilson, A., Genest Jr., J., Kastelein, J. J., Hayden, M. R.

المصدر: Circulation, 103 (9), 1198-1205 (2001)

مصطلحات موضوعية: ATP-Binding Cassette Transporters/ genetics, Lipids/blood, Lipoproteins/blood/ metabolism, Middle Aged, Phenotype, Polymorphism, Genetic, Single Nucleotide, Risk Factors, Severity of Illness Index, Survival Analysis, Humans, Genotype, Genetic Variation, Adult, Age Factors, Aged, Amino Acid Substitution, Body Mass Index, Cholesterol, HDL/metabolism, Cohort Studies, Coronary Disease/ genetics/pathology, Gene Frequency, Triglycerides/blood, Life sciences, Sciences du vivant

العلاقة: urn:issn:1524-4539; https://orbilu.uni.lu/handle/10993/26996Test; info:hdl:10993/26996; scopus-id:2-s2.0-0035814958; info:pmid:11238261; wos:000167562200006

الإتاحة: https://doi.org/10.1161/01.CIR.103.9.1198Test
https://orbilu.uni.lu/handle/10993/26996Test

المؤلفون: Rioux, J D, Daly, M J, Silverberg, M S, Lindblad, K, Steinhart, H, Cohen, Z, Delmonte, T, Brown, Kerry K, PhD, Miller, K, Guschwan, S, Kulbokas, E J, O'Leary, S, Winchester, E, Dewar, K, Green, T, Stone, V, Chow, C, Cohen, A, Langelier, D, Lapointe, G, Gaudet, D, Faith, J, Branco, N, Bull, S B, McLeod, R S, Griffiths, A M, Bitton, A, Greenberg, G R, Lander, E S, Siminovitch, K A, Hudson, T J

المصدر: Department of Pathology & Laboratory Medicine

مصطلحات موضوعية: Chromosome Mapping, Chromosomes, Human, Pair 5, Crohn Disease, Cytokines, Genetic Predisposition to Disease, Genetic Variation, Humans, Linkage Disequilibrium, Multigene Family, Polymorphism, Single Nucleotide, Department of Pathology and Laboratory Medicine, Medicine and Health Sciences

العلاقة: https://scholarlyworks.lvhn.org/pathology-laboratory-medicine/691Test; https://pubmed.ncbi.nlm.nih.gov/11586304Test/

الإتاحة: https://scholarlyworks.lvhn.org/pathology-laboratory-medicine/691Test
https://pubmed.ncbi.nlm.nih.gov/11586304Test/

المؤلفون: Xiong, L, Labuda, Małgorzata, Li, D S, Hudson, T J, Desbiens, Richard, Patry, G, Verret, S, Langevin, P, Mercho, S, Seni, M H, Scheffer, Ingrid E, Dubeau, Francois, Berkovic, S F, Andermann, Frederick, Andermann, Eva, Pandolfo, Massimo

المصدر: American journal of human genetics, 65 (6

مصطلحات موضوعية: Sciences bio-médicales et agricoles, Australia, Canada, Chromosome Mapping, Chromosomes, Human, Pair 22 -- genetics, Epilepsies, Partial -- genetics, Female, Founder Effect, Genes, Dominant -- genetics, Genetic Heterogeneity, Genetic Markers, Haplotypes -- genetics, Homozygote, Humans, Linkage (Genetics) -- genetics, Male, Pedigree, Penetrance, Polymorphism, Genetic -- genetics, Receptors, Purinergic P1 -- genetics, Recombination

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

العلاقة: uri/info:doi/10.1086/302649; uri/info:pii/S0002-9297(07)63590-3; uri/info:pmid/10577924; uri/info:pmcid/PMC1288381; https://dipot.ulb.ac.be/dspace/bitstream/2013/58629/4/PMC1288381.pdfTest; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/58629Test

الإتاحة: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/58629Test
https://dipot.ulb.ac.be/dspace/bitstream/2013/58629/4/PMC1288381.pdfTest

المؤلفون: Poon, A. H., Laprise, C., Lemire, M., Hudson, T. J., Schurr, E.

المصدر: Genes & Immunity; Sep2005, Vol. 6 Issue 6, p519-527, 9p

مصطلحات موضوعية: ASTHMATICS, TUBERCULOSIS, ACTINOMYCETALES, MYCOBACTERIA, ETIOLOGY of diseases

مصطلحات جغرافية: QUEBEC (Province)

المؤلفون: Kauppi, P., Lindblad-Toh, K., Sevon, P., Hannu Toivonen, Rioux, J. D., Villapakkam, A., Laitinen, L. A., Hudson, T. J., Juha Kere, Laitinen, T.

المساهمون: Department of Mathematics and Statistics, Department of Computer Science, Department of Medical and Clinical Genetics, Finnish Genome Center (-2009), Keuhkosairauksien yksikkö

المصدر: University of Helsinki

مصطلحات موضوعية: LINKAGE DISEQUILIBRIUM, JAPANESE, CHROMOSOME-5, education, atopy, association, SERUM IGE LEVELS, SIGNAL-TRANSDUCTION, asthma, haplotype pattern mining, SUSCEPTIBILITY, polymorphism, MARKERS, 311 Basic medicine, ALPHA-GENE, POLYMORPHISMS

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e684bed7edbccf59ca5f68d889bc67b7Test
https://researchportal.helsinki.fi/en/publications/0164cd0d-41e1-42b5-a05e-26edb843dac9Test