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1دورية أكاديمية
المؤلفون: Diaconu Rodica, Dumitrașcu Andreea-Ramona, Liehn Elisa, Pîrvu Andrei, Ioana Mihai, Alexandru Dragoș, Țieranu Eugen, Bălșeanu Tudor-Adrian, Donoiu Ionuț
المصدر: Romanian Journal of Cardiology, Vol 33, Iss 1, Pp 19-24 (2023)
مصطلحات موضوعية: apolipoprotein e, genotyping, allele variants, cardiovascular risk, apolipoproteină e, genotipare, variante de alele, risc cardiovascular, Internal medicine, RC31-1245
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2734-6382
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2دورية أكاديمية
المؤلفون: Eugeniu Russu, Liliana Groppa, Lia Chișlari, Victor Cazac, Larisa Rotaru
المصدر: Arta Medica, Vol 83, Iss 2 (2022)
مصطلحات موضوعية: artrita psoriazică, alele HLA, markerii imunogenetici, Medicine, Surgery, RD1-811
وصف الملف: electronic resource
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المؤلفون: Gregorčič, Tamara
المساهمون: Potočnik, Klemen
مصطلحات موضوعية: mleko, udc:575:637.1(043.2), govedo, kapa kazein, magistrske naloge, molekularna genetika, izražanje genov, alele, verjetnost
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3505::4f1349f6c9d2d2b88d801d39e1b408aa
https://repozitorij.uni-lj.si/IzpisGradiva.php?id=123522 -
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المؤلفون: Fojtíková, Markéta
المساهمون: Pavelka, Karel, Hrnčíř, Zbyněk, Rovenský, Jozef
مصطلحات موضوعية: Systemic lupus erythematosus, exprese, hlavní histokompatibilní systém, prolaktin, psoriatic arthritis, systemic sclerosis, prolactin, autoimmunity, dermatomyositis, major histocompatibility system, autoimunita, psoriatická artritida, polymyositis, alela, alele, dermatomyositida, rheumatoid arthritis, revmatoidní artritida, gen, association, polymorphism, polymyositida, asociace, Systémový lupus erythematodes, polymorfismus, systémová sklerodermie, gene, expression, skin and connective tissue diseases
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::447689c926670a038b82d91550ef490b
http://www.nusl.cz/ntk/nusl-441655 -
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المؤلفون: Volskienė, Rasa
المساهمون: Miceikienė, Ilona Teodora, Jukna, Česlovas, Bakutis, Bronius, Klimienė, Asta, Nainienė, Rasa, Tušas, Saulius, Juozaitienė, Vida, Sruoga, Aniolas, Lithuanian Veterinary Academy
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1338::66c03f09b918547c2744fd89d9850ab9
http://vddb.library.lt/fedora/get/LT-eLABa-0001:E.02~2008~D_20081215_130610-35367/DS.005.0.02.ETD -
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المؤلفون: Paolo Vezzoni, David Mellis, Julie C. Crockett, Fraser P. Coxon, Alessandra Pangrazio, Daniele Moratto, Evelina Mazzolari, Anna Villa, Mario Abinun, Paul J. Orchard, Jill Clayton-Smith, Luigi D. Notarangelo, Ilhan Tezcan, Michael J. Rogers, Barbara Cassani, Sara Sebnem Kilic, Miep H. Helfrich, Annalisa Frattini, Ashok Vellodi, Cristina Sobacchi, Matteo M Guerrini
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı/Çocuk İmmunoloji Bilim Dalı., Kılıç, Sara Şebnem, AAH-1658-2021, Çocuk Sağlığı ve Hastalıkları
المصدر: American journal of human genetics 83 (2008): 64–76. doi:10.1016/j.ajhg.2008.06.015
info:cnr-pdr/source/autori:Guerrini MM; Sobacchi C; Cassani B; Abinun M; Kilic SS; Pangrazio A; Moratto D; Mazzolari E; Clayton-Smith J; Orchard P; Coxon FP; Helfrich MH; Crockett JC; Mellis D; Vellodi A; Tezcan I; Notarangelo LD; Rogers MJ; Vezzoni P; Villa A; Frattini A./titolo:Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations./doi:10.1016%2Fj.ajhg.2008.06.015/rivista:American journal of human genetics/anno:2008/pagina_da:64/pagina_a:76/intervallo_pagine:64–76/volume:83مصطلحات موضوعية: Male, Turkey, DNA Mutational Analysis, Gene sequence, Monocyte, Hypogammaglobulinemia, Consanguinity, Receptor activator differentiation, Agammaglobulinemia, Genetics(clinical), Priority, Cell proliferation, Genetics & Heredity, Mutation, Colony stimulating factor 1, Antigens, CD45, Pedigree, Autosomal recessive osteopetrosis, Cohort studies, Osteoclast, Osteopetrosis, Osteopetrosis with Renal Tubular Acidosis, Chloride Channels, Leukocytes, mononuclear, Human, musculoskeletal diseases, Albers Schoenberg disease, Cells, Argentina, Radiography, thoracic, Receptors, vitronectin, Article, Ilium, Genetic, Genetics, Humans, Polymorphism, Receptor activator of nuclear factor-kappa B, RANK ligand, Polymorphism, Genetic, medicine.disease, Cell line, transformed, Immunology, İmmunological parameters, Nucleotide sequence, Lipopolysaccharides, Herpesvirus 4, Human, Journal, Amino acid substitution, Mutation, missense, Duplication, Biopsy, Osteoimmunology, Osteoclasts, medicine.disease_cause, Disease, Pakistan, İmmunoglobulin deficiency, Genetics (clinical), Tartrate-resistant acid phosphatase, biology, Macrophage colony-stimulating factor, Homozygote, Isoenzymes, medicine.anatomical_structure, RANKL, Female, Osteoclast differentiation factor, Alele, Cells, cultured, Heterozygote, Sibling, İmmune system, Genes, Recessive, Case-control studies, Sequence homology, amino Acid, Arginine, Cell transformation, viral, Amino acid sequence, Receptor activator of nuclear factor kappa B, Molecular sequence data, medicine, Acid phosphatase, Cysteine, Gene mutation, Human tissue, B lymphocyte, Tartrate-Resistant Acid Phosphatase, Models, immunological, İmmune deficiency, Osteoprotegerin, In vitro study, Dendrites, TCIRG1, Actins, biology.protein, Leukocyte Common Antigens, CLCN7, Protein structure, tertiary
وصف الملف: application/pdf; text/plain
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::868813390919efb5303f6e2b4af5955d
http://www.cnr.it/prodotto/i/56024 -
8مورد إلكتروني
المصدر: 6A
URL:
http://cdm16802.contentdm.oclc.org/cdm/ref/collection/p16802coll35/id/428972 http://cdm16802.contentdm.oclc.org/utils/getthumbnail/collection/p16802coll35/id/428972 http://worldcat.org/search?q=on:OCO+http://cdm16802.contentdm.oclc.org/oai/oai.php+p16802coll35+CNTCOLL http://worldcat.org/oclc/1182494417/viewonline
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