المؤلفون: Enrique R. Argañaraz, Antonio Carlos Rosário Vallinoto, Maria Alice Freitas Queiroz, Gustavo A. Argañaraz, Ricardo Ishak, Thalita Camêlo da Silva Ferreira

المصدر: International Journal of Infectious Diseases, Vol 65, Iss, Pp 67-71 (2017)

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Microbiology (medical), Genotype, Genotyping Techniques, Population, HIV Infections, Biology, Asymptomatic, lcsh:Infectious and parasitic diseases, 03 medical and health sciences, 0302 clinical medicine, Polymorphism (computer science), Ethnicity, medicine, Humans, lcsh:RC109-216, Lymphocyte Count, education, Genotyping, Human T-lymphotropic virus 1, education.field_of_study, Polymorphism, Genetic, virus diseases, General Medicine, Viral Load, HTLV-I Infections, Genotype frequency, 030104 developmental biology, Infectious Diseases, Case-Control Studies, alpha 1-Antitrypsin, 030220 oncology & carcinogenesis, DNA, Viral, Immunology, HIV-1, Female, medicine.symptom, Viral load, Brazil, Gene Deletion, CD8

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7099d60e969a1e0e339238d24e29805Test
https://doi.org/10.1016/j.ijid.2017.10.002Test

المؤلفون: Liying Jiang, C. Wang, Yidan Wang, Y. Tao, Jiesheng Rong, Xun Zhuang, B. Xing, Minjie Chu, Xiaoyue Zhu, S. Wang

المصدر: Osteoarthritis and Cartilage. 25:1062-1067

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Oncology, China, medicine.medical_specialty, Genotype, Population, Biomedical Engineering, Single-nucleotide polymorphism, Osteoarthritis, Polymorphism, Single Nucleotide, Aldehyde Dehydrogenase 1 Family, 03 medical and health sciences, 0302 clinical medicine, Rheumatology, Polymorphism (computer science), Internal medicine, medicine, Humans, SNP, Genetic Predisposition to Disease, Orthopedics and Sports Medicine, Allele, education, Aged, 030203 arthritis & rheumatology, Genetics, education.field_of_study, business.industry, Genetic Variation, Retinal Dehydrogenase, Odds ratio, Middle Aged, Osteoarthritis, Knee, medicine.disease, Confidence interval, 030104 developmental biology, Case-Control Studies, Female, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::344fb4ba8a401f3773053e7c6075144dTest
https://doi.org/10.1016/j.joca.2017.01.003Test

المؤلفون: Niloufar Mobashery, Julie Strizki, Carolyn McHale, Jacqueline D. Reeves, Amber A. Rivera, Richard J. O. Barnard, Amy L. Himmelberger, Mark J. DiNubile, David C. Nickle, Donald J. Graham, Peggy Hwang, William Newhard, Daria J. Hazuda, Carol A. Cheney

المصدر: Virology. 443:278-284

مصطلحات موضوعية: Cyclopropanes, Male, Indoles, Vaniprevir, Hepacivirus, Isoindoles, medicine.disease_cause, Gastroenterology, Polyethylene Glycols, chemistry.chemical_compound, Genotype, Treatment Failure, Sulfonamides, education.field_of_study, Hepatitis C-genotype 1, Hepatitis C, Middle Aged, Treatment Outcome, RNA, Viral, Drug Therapy, Combination, Female, Adult, medicine.medical_specialty, Adolescent, Proline, Lactams, Macrocyclic, Hepatitis C virus, Population, Viremia, Biology, Antiviral Agents, Treatment experienced, Young Adult, Double-Blind Method, Leucine, Virology, Internal medicine, Drug Resistance, Viral, Ribavirin, medicine, Humans, Dosing, education, Resistance-associated variants, Aged, Genetic Variation, Hepatitis C, Chronic, medicine.disease, Amino Acid Substitution, chemistry, Peptide Hydrolases

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7619ea624eb71d616e98034d1959625Test
https://doi.org/10.1016/j.virol.2013.05.013Test

المؤلفون: M. Portela, Céleste Lebbé, C. Vilmer, Louis Dubertret, Bernard Grandchamp, Gisele Delestaing, Nicole Basset-Seguin, Delphine Kerob, Isabelle Gorin, Muriel Liboutet, Nadem Soufir, Nicolas Dupin, Philippe Saiag

المصدر: Journal of Investigative Dermatology. 126:1510-1517

مصطلحات موضوعية: Adult, Male, Patched Receptors, Patched, Oncology, Pathology, medicine.medical_specialty, Skin Neoplasms, Ptch gene, Population, Receptors, Cell Surface, Dermatology, Biology, Biochemistry, White People, Gene Frequency, Risk Factors, Internal medicine, Genotype, Odds Ratio, medicine, Humans, Genetic Predisposition to Disease, Basal cell carcinoma, Prospective Studies, Allele, Hair Color, education, Molecular Biology, Aged, Aged, 80 and over, education.field_of_study, Polymorphism, Genetic, Cell Biology, Odds ratio, Middle Aged, medicine.disease, Patched-1 Receptor, Carcinoma, Basal Cell, Case-Control Studies, Regression Analysis, Female, France, Receptor, Melanocortin, Type 1, Melanocortin 1 receptor

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::853998703630af09d0130707b834887eTest
https://doi.org/10.1038/sj.jid.5700263Test

المؤلفون: Grant W. Montgomery, Manuel A. R. Ferreira, Allan F. McRae, Gu Zhu, Nicholas G. Martin, Jodie N. Painter, Narelle K. Hansell, Brian P. McEvoy, Stuart MacGregor, Wendy S. Slutske, Anjali K. Henders, Sarah E. Medland, Margaret J. Wright, Dale R. Nyholt, Megan Campbell, Andrew C. Heath, David L. Duffy, Scott D. Gordon

المصدر: The American Journal of Human Genetics. 85(5):750-755

مصطلحات موضوعية: Male, Linkage disequilibrium, Genome-wide association study, Inner root sheath, Linkage Disequilibrium, Cohort Studies, Methionine, 0302 clinical medicine, Gene Frequency, Intermediate Filament Proteins, Genetics(clinical), Child, Genetics (clinical), Genetics, 0303 health sciences, education.field_of_study, Geography, integumentary system, Trichohyalin, medicine.anatomical_structure, Chromosomes, Human, Pair 1, Female, Hair Follicle, Adult, Genetic Markers, Adolescent, Genotype, Molecular Sequence Data, Population, Biology, Polymorphism, Single Nucleotide, White People, Nuclear Family, Young Adult, 03 medical and health sciences, Meta-Analysis as Topic, Report, Genetic variation, medicine, Humans, Amino Acid Sequence, Protein Precursors, education, Alleles, 030304 developmental biology, Genome, Human, Haplotype, Australia, Genetic Variation, Hair follicle, Genetics, Population, Amino Acid Substitution, Haplotypes, Karyotyping, sense organs, 030217 neurology & neurosurgery, Genome-Wide Association Study, Hair

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6307ebacddf6e3d1de17f5fca162dc6Test

المؤلفون: Rami Kang, Sang Kun Lee, Dong Wook Kim, Manho Kim, Seo-Young Lee

المصدر: Seizure. 15(5):344-347

مصطلحات موضوعية: Adult, Male, Genotype, Population, Clinical Neurology, C3435T polymorphism, Multidrug resistance, Polymorphism, Single Nucleotide, Epilepsy, Gene Frequency, Medicine, Humans, ATP Binding Cassette Transporter, Subfamily B, Member 1, Allele, education, Allele frequency, Gene, Alleles, Genetics, education.field_of_study, Korea, business.industry, General Medicine, medicine.disease, Drug Resistance, Multiple, Multiple drug resistance, Neurology, Female, Neurology (clinical), Gene polymorphism, Genes, MDR, Korean population, business, MDR1 gene

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56f57ddb086567115b0adf4c84e64e09Test

المؤلفون: Prachiya Jewhasuchin, Noritaka Oyama, Takahiro Hamada, Devinder Mohan Thappa, John A. McGrath, Bernice R. Krafchik, Hiroshi Shimizu, S Charuwichitratana, Mauro Paradisi, Andrew P. South, Kanokvalai Kulthanan, G H S Ashton, Vesarat Wessagowit, Apatorn Siriwattana, Ien Chan, Tamer Irfan Kaya, Patsy Lenane, Amy S. Paller, Takashi Hashimoto, Mehmet Emin Erdal, Mariko Seishima

المصدر: Journal of Investigative Dermatology. 120:345-350

مصطلحات موضوعية: Adult, Male, Heterozygote, Adolescent, Genotype, Mutation, Missense, Dermatology, Biology, Compound heterozygosity, Biochemistry, Frameshift mutation, alternative splicing, Exon, Extracellular matrix protein 1, genodermatosis hyalinosis cutis et mucosae, medicine, Humans, Frameshift Mutation, education, Molecular Biology, Genetics, Extracellular Matrix Proteins, education.field_of_study, Polymorphism, Genetic, Base Sequence, Reverse Transcriptase Polymerase Chain Reaction, Homozygote, Haplotype, Alternative splicing, Genodermatosis, Exons, Cell Biology, Middle Aged, medicine.disease, Phenotype, Haplotypes, Codon, Nonsense, Child, Preschool, Mutation, Lipoid Proteinosis of Urbach and Wiethe, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::137dfbf6f90672842d8daa334991cc32Test
https://doi.org/10.1046/j.1523-1747.2003.12073.xTest

المؤلفون: Julie M. Cunningham, Eric R. Christensen, Daniel J. Schaid, Stephen N. Thibodeau, Susan L. Slager, Steven J. Jacobsen, Angela F. Marks, Michael L. Blute, Liang Wang, James R. Cerhan, David A. Elkins, Brett J. Peterson, Shannon K. McDonnell

المصدر: The American Journal of Human Genetics. 71:116-123

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Candidate gene, Molecular Sequence Data, Population, Biology, Gastroenterology, MSR1, Polymorphism (computer science), Internal medicine, Endoribonucleases, Genotype, Genetics, medicine, Humans, Genetics(clinical), education, Allele frequency, Alleles, Germ-Line Mutation, Genetics (clinical), Aged, Aged, 80 and over, education.field_of_study, Base Sequence, Genetic Variation, Prostatic Neoplasms, RNASEL Gene, Exons, Articles, Odds ratio, Middle Aged, Introns, Endocrinology, Chromosomes, Human, Pair 1, Case-Control Studies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1740f955fc8690a78c4be1bd7bffb29Test
https://doi.org/10.1086/341281Test