Zobrazeno 1 - 10
of 189
pro vyhledávání: '"CCL3L1"'
Autor:
Ahmed Hieran, Bushra Jabbar Albadry
Publikováno v:
مجلة علوم ذي قار, Vol 10, Iss 1 (2023)
The CCL3L1 gene plays an important role in regulating immunity against many pathogens. The aim of this study, which was conducted in Thi-Qar province from February 2022 to February 2023, was to estimate the gene expression of the CCL3L1 gene in peopl
Externí odkaz:
https://doaj.org/article/f076f6fcd0b44b0dbd8870af05d55241
Autor:
Jalilah Jamaluddin, Nur Khairina Mohd Khair, Shameni Devi Vinodamaney, Zulkefley Othman, Suhaili Abubakar
Publikováno v:
BMC Genetics, Vol 21, Iss 1, Pp 1-8 (2020)
Abstract Background C-C motif Chemokine Ligand 3 Like 1 (CCL3L1) is a multiallelic copy number variable, which plays a crucial role in immunoregulatory and hosts defense through the production of macrophage inflammatory protein (MIP)-1α. Variable ra
Externí odkaz:
https://doaj.org/article/b1a00a0039574d4e8bec7a03c3289de1
Autor:
Dong-Eun Lee, Hye-Won Sim, Eunyoung Emily Lee, Yeong Wook Song, Kyeong-Man Hong, Young Ho Kim, Eun-Kyung Kang, Yoon-Ho Won
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Scientific Reports
Scientific Reports
The correlation between copy number variation (CNV) and the susceptibility to systemic lupus erythematosus (SLE) has been reported for various immunity-related genes. However, the contribution of CNVs to SLE susceptibility awaits more investigation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::520000d929087773c6d51cd288841f13
https://doaj.org/article/476cd58f043043d6a01ce297736735e1
https://doaj.org/article/476cd58f043043d6a01ce297736735e1
Publikováno v:
Molecular Diagnosis & Therapy
Introduction It has been proposed that the copy number (CN) variation (CNV) in β-defensin genes (DEFB) on human chromosome 8p23 determines phenotypic differences in inflammatory diseases. However, no method for accurate and easy DEFB CN quantificati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4664130f0843858b6fb9e4c29e3c4187
https://doi.org/10.1007/s40291-021-00546-2
https://doi.org/10.1007/s40291-021-00546-2
The CNVrd2 package: measurement of copy number at complex loci using high-throughput sequencing data
Publikováno v:
Frontiers in Genetics, Vol 5 (2014)
Recent advances in high-throughout sequencing technologies have made it possible to accurately assign copy number (CN) at CN variable loci. However, current analytic methods often perform poorly in regions in which complex CN variation is observed. H
Externí odkaz:
https://doaj.org/article/baa4848508c345a8926beba72787c388
Akademický článek
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SLAMF7 Is a Critical Negative Regulator of IFN-α–Mediated CXCL10 Production in Chronic HIV Infection
Autor:
Patrick O'Connell, Maja K Blake, Yasser A. Aldhamen, Michael D. Rizzo, Andrea Amalfitano, Yuliya Pepelyayeva, Linda Dale, Norbert E. Kaminski, Peter Gulick, Cristiane Pereira-Hicks, Sarah Godbehere, Robert B. Crawford, Sean Hyslop
Publikováno v:
The Journal of Immunology. 202:228-238
Current advances in combined antiretroviral therapy have rendered HIV infection a chronic, manageable disease; however, the problem of persistent immune activation still remains despite treatment. The immune cell receptor SLAMF7 has been shown to be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdaca4bf6eeca147cc959e5ece5f3101
https://doi.org/10.4049/jimmunol.1800847
https://doi.org/10.4049/jimmunol.1800847
Publikováno v:
European Journal of Human Genetics. 26:886-897
Copy number variations (CNVs) are genomic structural variations that result from the deletion or duplication of large genomic segments. The characterization of CNVs is largely underrepresented, particularly those of indigenous populations, such as th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b389432470187557df19e879c32efe35
https://doi.org/10.1038/s41431-018-0120-8
https://doi.org/10.1038/s41431-018-0120-8
Publikováno v:
Oncotarget
// Yanting Shen 1, 2 , Lu Bu 3 , Rui Li 1 , Zhenzhu Chen 1 , Fei Tian 1 , Na Lu 2 , Qinyu Ge 2 , Yunfei Bai 2 , Zuhong Lu 1, 2 1 Research Center for Learning Science, Southeast University, Nanjing, Jiangsu Province 210096, PR China 2 State Key Labora
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac47354176639456d9506daacaac95dc
http://europepmc.org/articles/PMC5438623
http://europepmc.org/articles/PMC5438623
Autor:
Knight, Julian C., author
Publikováno v:
Human Genetic Diversity : Functional Consequences for Health and Disease, 2009, ill.
Externí odkaz:
https://doi.org/10.1093/acprof:oso/9780199227693.003.0014