المؤلفون: Jianing Lin, Pian Huang, Weineng Chen, Chenghui Ye, Huanxing Su, Xiaoli Yao

المصدر: Frontiers in Genetics, Vol 11 (2020)

مصطلحات موضوعية: sporadic amyotrophic lateral sclerosis, gene expression profiles, motor neurons, bioinformatics analysis, FN1 gene, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2020.578143/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/2834d9ace5b649c08c4a02fe145574c5

المؤلفون: Hu S., Parker J., Wright J.T.

المساهمون: DEAN'S OFFICE (DENTISTRY), DENTISTRY

المصدر: Unpaywall 20191101

مصطلحات موضوعية: dentome, mitogen activated protein kinase 7, phospholipase C, RNA, transcriptome, unclassified drug, ameloblast, AMELX gene, Article, ASTN1 gene, cell isolation, cell motility, cell motion, cells by body anatomy, COL1A1 gene, controlled study, developmental stage, enamel, fetus, FN1 gene, gene, gene expression, gestational age, human, human cell, human tissue, laser capture microdissection, LUM gene, microarray analysis, molecular mechanics

Relation: Hu S., Parker J., Wright J.T. (2015). Towards unraveling the human tooth transcriptome: The dentome. PLoS ONE 10 (4) : e0124801. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0124801; https://scholarbank.nus.edu.sg/handle/10635/161524

الاتاحة: https://scholarbank.nus.edu.sg/handle/10635/161524

المؤلفون: Chenghui Ye, Pian Huang, Jianing Lin, Weineng Chen, Xiaoli Yao, Huanxing Su

المصدر: Frontiers in Genetics, Vol 11 (2020)
Frontiers in Genetics

مصطلحات موضوعية: 0301 basic medicine, bioinformatics analysis, Bioinformatics analysis, lcsh:QH426-470, Blood vessel morphogenesis, Biology, FN1 gene, Pathogenesis, Extracellular matrix, 03 medical and health sciences, 0302 clinical medicine, sporadic amyotrophic lateral sclerosis, Gene expression, Genetics, medicine, motor neurons, Amyotrophic lateral sclerosis, Transcription factor, Genetics (clinical), Original Research, gene expression profiles, medicine.disease, lcsh:Genetics, 030104 developmental biology, 030220 oncology & carcinogenesis, Molecular Medicine, Regulatory Pathway, Neuroscience

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b08b132214bcfe05791c1c5db343d950
https://www.frontiersin.org/articles/10.3389/fgene.2020.578143/full

المؤلفون: Cohen, Evan N, Gao, Hui, Anfossi, Simone, Mego, Michal, Reddy, Neelima G, Debeb, Bisrat, Giordano, Antonio, Tin, Sanda, Wu, Qiong, Garza, Raul J, Cristofanilli, Massimo, Mani, Sendurai A, Croix, Denise A, Ueno, Naoto T, Woodward, Wendy A, Luthra, Raja, Krishnamurthy, Savitri, Reuben, James M

المصدر: Department of Medical Oncology Faculty Papers

مصطلحات موضوعية: Medical Oncology, Thomas Jefferson University, Article, cancer cell culture, cell invasion, cell migration, circulating tumor cell, clinical article, controlled study, cytokine production, epithelial mesenchymal transition, FN1 gene, gene expression, human, human cell, human tissue, immunocompetent cell, inflammatory breast cancer, marker gene, metastasis, protein expression, T lymphocyte activation, TGM2 gene, VIM gene, ZEB1 gene, Oncology

وصف الملف: application/pdf

Relation: https://jdc.jefferson.edu/medoncfp/44; https://jdc.jefferson.edu/context/medoncfp/article/1043/viewcontent/inflammatory_breast_cancer_cells.pdf

الاتاحة: https://jdc.jefferson.edu/medoncfp/44
https://jdc.jefferson.edu/context/medoncfp/article/1043/viewcontent/inflammatory_breast_cancer_cells.pdf

المؤلفون: Constantinou-Deltas, Constantinos D., Pierides, Alkis M., Voskarides, Konstantinos

المساهمون: Constantinou-Deltas, Constantinos D. [0000-0001-5549-9169]

المصدر: Nephrology Dialysis Transplantation
Nephrol.Dial.Transplant.

مصطلحات موضوعية: COL5A5 gene, Genetic modifiers, COL4-CFHR5-FN1, kidney disease, genetic analysis, urologic and male genital diseases, glomerulopathy with fibronectin deposits, X chromosome recessive inheritance, genetic variability, protein complement factor H related 5, gene mutation, familial disease, chromosome map, Glomerular basement membrane, thin basement membrane nephropathy, COL4A1 gene, complement factor H, COL4A4 gene, Glomerulonephritis, phenotypic variation, Penetrance, unclassified drug, medicine.anatomical_structure, priority journal, Nephrology, CFHR5 gene, Genetic and phenotypic heterogeneity, Biological Markers, immunoreactivity, Thin basement membrane disease, Collagen Type IV, review, Biology, glomerulopathy, FN1 gene, histology, collagen type 4, Glomerulopathy, fibronectin, c3 glomerulonephritis, medicine, Humans, human, Alport syndrome, end stage renal disease, Molecular Biology, COL4A3 gene, Hematuria, Transplantation, modifier gene, nonhuman, Genetic heterogeneity, missense mutation, Complement System Proteins, medicine.disease, Alport-TBMN-CFHR5/C3GN-GFND, Fibronectins, Familial microscopic hematuria, hematuria, glomerular filtration barrier, Immunology, molecular genetics, Mutation, familial hematuric disease, proteinuria, CFHR5, Biomarkers, glomerulonephritis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2595998b2b8b377a83e9aca8ed6486ac
http://gnosis.library.ucy.ac.cy/handle/7/53032