المؤلفون: Jie Zhou, Peiwei Li, Xiaogang Zhao, Yuanhao Zhao, Junwen Luo, Yupeng Deng, Ning Jiang, Zhaohua Xiao, Wenhao Zhang, Yongjia Zhou, Jiangfeng Zhao, Peichao Li, Yuliang Li, Zhongxian Tian

المصدر: Respiratory Research, Vol 24, Iss 1, Pp 1-17 (2023)

مصطلحات موضوعية: Circ_16601, miR-5580-5p, LUAD, FGB, HIPPO pathway, My-CAF, Diseases of the respiratory system, RC705-779

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1465-993XTest

الوصول الحر: https://doaj.org/article/b8a1e3aa4bf0451fa1320785b3281376Test

المؤلفون: Cavalli, M., Diamanti, K., Pan, G., Spalinskas, Rapolas, Dr., 1983, Kumar, C., Deshmukh, A. S., Mann, M., Sahlén, Pelin, Komorowski, J., Wadelius, C.

المصدر: Omics. 24(4):180-194

مصطلحات موضوعية: human liver, multi-omics data integration, proteomics, snRNA-seq, ADAMTS protein, ADAMTS2 protein, albumin, biological marker, cadherin, cadherin 11, CD163 antigen, CD74 antigen, collagen type 3, collagen type 6, cystic fibrosis transmembrane conductance regulator, dihydropyrimidine dehydrogenase, epithelial cell adhesion molecule, fibroblast growth factor 1, fluorouracil, glucose transporter 1, glucose transporter 2, interleukin 18, messenger RNA, nostrin, proteome, small nuclear RNA, somatomedin binding protein 3, transcription factor Sox4, transcription factor Sox9, transcriptome, unclassified drug, vasculotropin receptor 1, apoa2 gene, Article, c3 gene, controlled study, dcn gene, enhancer region, eps2 gene, f5 gene, f8 gene, fgb gene, fgl1 gene, g6pc gene, gene, gene identification, human, human cell, human chromosome, human tissue, intron, lamb1 gene, liver cell carcinoma, liver parenchyma, lrp2 gene, marker gene, mass spectrometry, multiomics, mup3 gene, myo1f gene, oit3 gene, pck1 gene, plekhg1 gene, plg gene, priority journal, promoter region, ptprb gene, RNA conformation, RNA sequencing, single nucleotide polymorphism, spp1 gene, transcriptomics

وصف الملف: print

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-277233Test
https://doi.org/10.1089/omi.2019.0215Test

المؤلفون: Zhang Y, Chen X, Cao Y, Yang Z

المصدر: Cancer Management and Research, Vol Volume 13, Pp 3503-3515 (2021)

مصطلحات موضوعية: c8b, fgb, complement and coagulation cascades, hepatocellular carcinoma, survival., Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

العلاقة: https://www.dovepress.com/c8b-in-complement-and-coagulation-cascades-signaling-pathway-is-a-pred-peer-reviewed-fulltext-article-CMARTest; https://doaj.org/toc/1179-1322Test

الوصول الحر: https://doaj.org/article/a73896f490974c72a23b23193c0cce9bTest

المؤلفون: N. N. Mavlyanova

المصدر: Juvenis Scientia, Vol 7, Iss 2, Pp 12-17 (2021)

مصطلحات موضوعية: pregnancy, placental insufficiency, genetics, polymorphism, fgb gene, Science, Medicine, History of scholarship and learning. The humanities, AZ20-999

وصف الملف: electronic resource

العلاقة: https://jscientia.org/index.php/js/article/view/48Test; https://doaj.org/toc/2414-3782Test; https://doaj.org/toc/2414-3790Test

الوصول الحر: https://doaj.org/article/36e3141ff7ca42f1b1992298efe35ff0Test

المؤلفون: S. D. Mayanskaya, L. A. Garaeva, A. T. Teplyakov, M. L. Filipenko, E. A. Sokolova, O. A. Kravtsova, E. V. Berezikova

المصدر: Бюллетень сибирской медицины, Vol 19, Iss 4, Pp 130-137 (2021)

مصطلحات موضوعية: повторный инфаркт миокарда, полиморфизм генов, tnfα, il1b, tgfb1b, fgb, itgb3, lpl, Medicine

وصف الملف: electronic resource

العلاقة: https://bulletin.ssmu.ru/jour/article/view/4160Test; https://doaj.org/toc/1682-0363Test; https://doaj.org/toc/1819-3684Test

الوصول الحر: https://doaj.org/article/05d8f645a58a4f2b8873befc1e3eab9cTest

المؤلفون: Nazirova V.

المصدر: POLISH JOURNAL OF SCIENCE 50 49-55

مصطلحات موضوعية: arterial hypertension, dyslipidemia, fibrinogen gene FGB, polymorphism, genotype, odds ratio

العلاقة: https://zenodo.org/record/6557477Test; https://doi.org/10.5281/zenodo.6557477Test; oai:zenodo.org:6557477

الإتاحة: https://doi.org/10.5281/zenodo.6557477Test
https://doi.org/10.5281/zenodo.6557476Test
https://zenodo.org/record/6557477Test

المؤلفون: Eliška Ceznerová, Jiřina Kaufmanová, Žofie Sovová, Jana Štikarová, Jan Loužil, Roman Kotlín, Jiří Suttnar

المصدر: International Journal of Molecular Sciences; Volume 23; Issue 2; Pages: 721

مصطلحات موضوعية: congenital fibrinogen disorder, FGB, hypofibrinogenemia, afibrinogenemia, dysfibrinogenemia, functional assays, scanning electron microscopy, homology modeling

جغرافية الموضوع: agris

وصف الملف: application/pdf

العلاقة: Macromolecules; https://dx.doi.org/10.3390/ijms23020721Test

الإتاحة: https://doi.org/10.3390/ijms23020721Test

المؤلفون: Fager Ferrari, Marcus

المصدر: Lund University, Faculty of Medicine Doctoral Dissertation Series. (2021:67)

مصطلحات موضوعية: Bleeding, Inherited Bleeding Disorders, Platelet Dysfunction, Thrombocytopenia, Genetic Screening, High-Throughput Sequencing, STX11, STXBP2, UNC13D, FGB, COL1A1, COL3A1, COL5A1, COL5A2, GNE, Sialic Acid, Oseltamivir, Medicin och hälsovetenskap, Klinisk medicin, Hematologi, Medical and Health Sciences, Clinical Medicine, Hematology

وصف الملف: electronic

الوصول الحر: https://lup.lub.lu.se/record/ad71c20f-76b8-4791-acf7-9c1c98c9aaf5Test
https://portal.research.lu.se/files/97548661/Marcus_Fager_Ferrari_WEBB.pdfTest

المؤلفون: Shengbin Han (11500345), Bin Yang (103252), Yaoyu Feng (142393), Lingfeng Zhao (11500348), Qun Feng (9427479), Hongxi Guan (11500351), Donghui Song (796642), Fang Yin (197561), Li Zhuang (120307)

مصطلحات موضوعية: Cardiology, Pharmacology and Pharmaceutical Sciences not elsewhere classified, fibrinogen β, single nucleotide polymorphisms, lower extremity deep venous thrombosis, FGB promoter polymorphism

العلاقة: https://figshare.com/articles/journal_contribution/Supplemental_Material_sj-pdf-1-cat-10_1177_1076029620967108_-_The_Correlation_Between_FGB_Promoter_Polymorphism_and_Clotting_Function_in_Patients_With_Idiopathic_Lower_Extremity_Deep_Venous_Thrombosis/16698739Test

الإتاحة: https://doi.org/10.25384/sage.16698739.v1Test

المؤلفون: Simurda T., Brunclikova M., Asselta R., Caccia S., Zolkova J., Kolkova Z., Loderer D., Skornova I., Hudecek J., Lasabova Z., Stasko J., Kubisz P.

المساهمون: T. Simurda, M. Brunclikova, R. Asselta, S. Caccia, J. Zolkova, Z. Kolkova, D. Loderer, I. Skornova, J. Hudecek, Z. Lasabova, J. Stasko, P. Kubisz

مصطلحات موضوعية: Beta and gamma nodule, FGB gene, FGG gene, Fibrinogen, Mutations associated with thrombosi, Quantitative fibrinogen disorders, Settore BIO/11 - Biologia Molecolare, Settore MED/03 - Genetica Medica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32610551; info:eu-repo/semantics/altIdentifier/wos/WOS:000550275900001; volume:21; issue:13; firstpage:1; lastpage:19; numberofpages:19; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; http://hdl.handle.net/2434/768952Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85087114562

الإتاحة: https://doi.org/10.3390/ijms21134616Test
http://hdl.handle.net/2434/768952Test