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المؤلفون: Yazun Jarrar, Sawsan I. Khdair, Omar Al-Khaldi, Wassan Jarrar, Safa’a Bataineh
المصدر: Endocrine, Metabolic & Immune Disorders - Drug Targets. 20:895-902
مصطلحات موضوعية: Adult, Male, musculoskeletal diseases, 0301 basic medicine, Adolescent, Genotype, endocrine system diseases, Endocrinology, Diabetes and Metabolism, Human leukocyte antigen, Biology, Lower risk, HLA-DQ alpha-Chains, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, immune system diseases, HLA-DQ Antigens, Diabetes mellitus, medicine, HLA-DQ beta-Chains, Humans, Immunology and Allergy, Genetic Predisposition to Disease, Allele, skin and connective tissue diseases, HLA-DRB1, Alleles, Genetic Association Studies, Type 1 diabetes, Jordan, Haplotype, nutritional and metabolic diseases, medicine.disease, Diabetes Mellitus, Type 1, 030104 developmental biology, Haplotypes, Case-Control Studies, Immunology, Female, HLA-DRB1 Chains, 030215 immunology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb55b44d9dfc2ddc969947a091621f2cTest
https://doi.org/10.2174/1871530319666191119114031Test -
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المؤلفون: Ravinder Goswami, Ajay Sood, R. Rani
المصدر: Tissue Antigens. 64:145-155
مصطلحات موضوعية: Adult, Male, musculoskeletal diseases, Adolescent, Immunology, Antigen presentation, India, Human leukocyte antigen, Biology, Major histocompatibility complex, Biochemistry, immune system diseases, Diabetes mellitus, Genetics, medicine, Humans, Immunology and Allergy, Genetic Predisposition to Disease, Allele, skin and connective tissue diseases, Alleles, Type 1 diabetes, HLA-DR Antigens, General Medicine, medicine.disease, Variable number tandem repeat, Diabetes Mellitus, Type 1, biology.protein, Female, Restriction fragment length polymorphism, HLA-DRB1 Chains
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::070cacffd4c5a7ebedff86f206376fecTest
https://doi.org/10.1111/j.1399-0039.2004.00246.xTest -
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المؤلفون: Nikhil Tandon, Neeraj Kumar, Gurvinder Kaur, Narinder K. Mehra
المصدر: Human Immunology. 73:566-573
مصطلحات موضوعية: Adult, Male, Linkage disequilibrium, Adolescent, endocrine system diseases, Immunology, Population, HLA-DR3, Single-nucleotide polymorphism, Human leukocyte antigen, Biology, Polymorphism, Single Nucleotide, Linkage Disequilibrium, HLA-DR3 Antigen, Gene Frequency, immune system diseases, Humans, Immunology and Allergy, Genetic Predisposition to Disease, Age of Onset, Allele, Child, education, Allele frequency, Alleles, Genetics, education.field_of_study, Tumor Necrosis Factor-alpha, Haplotype, nutritional and metabolic diseases, General Medicine, Middle Aged, Diabetes Mellitus, Type 1, Haplotypes, Genetic Loci, Case-Control Studies, Female, 5' Untranslated Regions, Microsatellite Repeats
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82a7b23663374991855fd67cba07164dTest
https://doi.org/10.1016/j.humimm.2012.01.012Test -
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المؤلفون: Taro Maruyama, Yasuko Nakano, Matsuo Taniyama, Teruaki Tozaki, Yoshiyuki Ban
المصدر: Human Immunology. 71:795-798
مصطلحات موضوعية: Adult, Male, endocrine system, Linkage disequilibrium, Genotype, endocrine system diseases, Immunology, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Linkage Disequilibrium, PTPN22, Asian People, Gene Frequency, Japan, immune system diseases, Genetic predisposition, Humans, Immunology and Allergy, Genetic Predisposition to Disease, Allele, Allele frequency, Alleles, Genetics, Haplotype, nutritional and metabolic diseases, Protein Tyrosine Phosphatase, Non-Receptor Type 22, General Medicine, Diabetes Mellitus, Type 1, Haplotypes, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52cbded95e50e4964a0c8805d6755176Test
https://doi.org/10.1016/j.humimm.2010.05.016Test -
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المؤلفون: Kadri Haller, Ele Prans, Raivo Uibo, Konstantinos Douroudis, Kalle Kisand, Tarvo Rajasalu, V. Nemvalts, Vallo Tillmann
المصدر: Tissue Antigens. 72:425-430
مصطلحات موضوعية: Adult, Estonia, Male, musculoskeletal diseases, Genotype, endocrine system diseases, Immunology, Population, Single-nucleotide polymorphism, Protein tyrosine phosphatase, Biology, Polymorphism, Single Nucleotide, Biochemistry, PTPN22, immune system diseases, Genetics, Humans, Immunology and Allergy, Genetic Predisposition to Disease, Allele, skin and connective tissue diseases, education, Gene, Alleles, Aged, education.field_of_study, nutritional and metabolic diseases, Protein Tyrosine Phosphatase, Non-Receptor Type 22, General Medicine, Middle Aged, PTPN11, Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2, Case-Control Studies, Female, TCF7L2
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a61686498f587d2577f42f1d72a27888Test
https://doi.org/10.1111/j.1399-0039.2008.01115.xTest -
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المؤلفون: Charles R. M. Bangham, Mineki Saito, Koichiro Usuku, Wataru Matsumoto, Shuji Izumo, Daisuke Kodama, Mitsuhiro Osame, Amir H. Sabouri, Kimiyoshi Arimura
المصدر: Journal of Neuroimmunology. 156:188-194
مصطلحات موضوعية: Adult, Male, T cell, Immunology, Biology, Jurkat Cells, Transactivation, Myelopathy, Risk Factors, immune system diseases, hemic and lymphatic diseases, Tropical spastic paraparesis, medicine, Humans, Immunology and Allergy, Allele, Dinucleotide Repeats, Promoter Regions, Genetic, Human T-lymphotropic virus 1, Polymorphism, Genetic, virus diseases, Promoter, Gene Products, tax, Middle Aged, medicine.disease, Paraparesis, Tropical Spastic, medicine.anatomical_structure, Matrix Metalloproteinase 9, Neurology, Htlv i associated myelopathy, Neurology (clinical), Asymptomatic carrier
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e988a7e351e70c91a2e2925a7ec2745Test
https://doi.org/10.1016/j.jneuroim.2004.07.007Test -
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المؤلفون: H. Shbaklo, Tony G. Zreik, G. Halaby, Sami T. Azar, Henry Terwedow, Pierre Zalloua, Antoine Abchee
المصدر: Human Immunology. 65:719-724
مصطلحات موضوعية: Adult, Male, Heterozygote, Adolescent, Genotype, endocrine system diseases, Immunology, Population, chemical and pharmacologic phenomena, Human leukocyte antigen, Biology, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, law.invention, Exon, Gene Frequency, Antigens, CD, immune system diseases, law, HLA-DQ Antigens, HLA-DQ beta-Chains, Humans, Immunology and Allergy, CTLA-4 Antigen, Genetic Predisposition to Disease, Age of Onset, Lebanon, Allele, Child, education, Polymerase chain reaction, Genetic association, Genetics, education.field_of_study, Homozygote, Haplotype, nutritional and metabolic diseases, DNA, Exons, General Medicine, Antigens, Differentiation, Diabetes Mellitus, Type 1, Child, Preschool, Data Interpretation, Statistical, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35e17f982689e673f64f40a9004c56a5Test
https://doi.org/10.1016/j.humimm.2004.04.007Test -
8
المؤلفون: Abdul-Qader Al-Irhayim, Touhami Mahjoub, Jihen Benmansour, Wassim Y. Almawi, Mouna Stayoussef, Hichem B. Said, Chiheb B. Rayana
مصطلحات موضوعية: Microbiology (medical), musculoskeletal diseases, Adult, Male, Tunisia, endocrine system diseases, Adolescent, Clinical Biochemistry, Immunology, Human leukocyte antigen, Biology, Polymerase Chain Reaction, Young Adult, Gene Frequency, immune system diseases, HLA-DQ Antigens, Genotype, Genetic predisposition, medicine, Immunology and Allergy, Clinical Laboratory Immunology, HLA-DQ beta-Chains, Humans, Genetic Predisposition to Disease, Allele, skin and connective tissue diseases, Child, Genotyping, Retrospective Studies, Genetics, Type 1 diabetes, Polymorphism, Genetic, Haplotype, Case-control study, nutritional and metabolic diseases, HLA-DR Antigens, Sequence Analysis, DNA, medicine.disease, Diabetes Mellitus, Type 1, Haplotypes, Case-Control Studies, Female, HLA-DRB1 Chains
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f2c64d687b816ee2bb736eb39dbb958Test
https://europepmc.org/articles/PMC2725529Test/ -
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المؤلفون: Maria Elizabeth Rossi da Silva, Silvia Barbosa Dutra Marques, Sophie Caillat-Zucman, Walkyria Mara Gonçalves Volpini, Sofia Helena Valente de Lemos Marini, Gil Guerra, Maria Fernanda Vanti Macedo Paulino, Ligia B.L. Persoli, L. I. Alves, Giuliana V. Testa, Sergio Atala Dib
المصدر: Human Immunology. 62:1226-1233
مصطلحات موضوعية: Adult, Male, musculoskeletal diseases, Adolescent, Genotype, endocrine system diseases, Genes, MHC Class II, Immunology, Population, Human leukocyte antigen, Biology, HLA-DQ alpha-Chains, immune system diseases, HLA-DQ Antigens, HLA-DQ beta-Chains, Humans, Immunology and Allergy, Allele, Child, skin and connective tissue diseases, education, Genotyping, Alleles, Genetics, education.field_of_study, Haplotype, nutritional and metabolic diseases, Heterozygote advantage, HLA-DR Antigens, General Medicine, Subtyping, Diabetes Mellitus, Type 1, Haplotypes, Female, Brazil, HLA-DRB1 Chains
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d2b9781124fc1cca5ae0235ee2f2491Test
https://doi.org/10.1016/s0198-8859Test(01)00323-8 -
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المؤلفون: Novella Rapini, E. Del Duca, A. Maccari, G. Canu, M. L. Manca Bitti, Luigi Fontana, Alberto Verrotti, F. Angelini, Patrizia Saccucci, Nunzio Bottini, F. Chiarelli, Simona Piccinini, Cosimo Giannini
مصطلحات موضوعية: Male, endocrine system diseases, Autoimmunity, Protein tyrosine phosphatase, medicine.disease_cause, Biochemistry, Gene Frequency, immune system diseases, Missense mutation, Immunology and Allergy, Child, Genetics, General Medicine, Single Nucleotide, PTPN22, Non-Receptor Type 22, Type 1 diabetes, Italy, Female, Type 1, Adult, Italian, Adolescent, Immunology, Mutation, Missense, C1858T, Replication, Biology, Polymorphism, Single Nucleotide, Settore MED/01 - Statistica Medica, medicine, Diabetes Mellitus, Humans, Genetic Predisposition to Disease, Allele, Polymorphism, LYP, Alleles, Amino Acid Substitution, Base Sequence, Case-Control Studies, DNA Primers, Diabetes Mellitus, Type 1, Protein Tyrosine Phosphatase, Non-Receptor Type 22, Allele frequency, Case-control study, nutritional and metabolic diseases, medicine.disease, Mutation, Protein Tyrosine Phosphatase, Missense
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9f92927faf7850fa9d4bfb13acb1ed6Test
http://hdl.handle.net/11391/1230181Test