المؤلفون: Yuxiang Lin, Yan Li, Xiaobin Chen, Xuan Jin, Meichen Jiang, Han Xiao, Lili Chen, Minyan Chen, Wenzhe Zhang, Hanxi Chen, Qian Nie, Rongrong Guo, Wenhui Guo, Fangmeng Fu, Chuan Wang

المصدر: Biology Direct, Vol 19, Iss 1, Pp 1-16 (2024)

مصطلحات موضوعية: Triple-negative breast cancer, Progression, DCUN1D5, FN1, YY1, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1745-6150

URL الوصول: https://doaj.org/article/7531b162e1214b1f971fa4f7eea9ad04

المؤلفون: Oh, Jagyeong, Pradella, Davide, Shao, Changwei, Li, Hairi, Choi, Namjeong, Ha, Jiyeon, Ruggiero, Sonia, Fu, Xiang-Dong, Zheng, Xuexiu, Ghigna, Claudia, Shen, Haihong

المصدر: Cells. 10(4)

مصطلحات موضوعية: DCUN1D5, alternative splicing, breast cancer, cancer metastasis, exon skipping

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/4sm1z3px

المؤلفون: Lin, Yuxiang^{Aff1, Aff2, Aff3}, Li, Yan^{Aff1, Aff2, Aff3}, Chen, Xiaobin^{Aff1, Aff2, Aff3}, Jin, Xuan^{Aff1, Aff2, Aff3}, Jiang, Meichen, Xiao, Han, Chen, Lili^{Aff1, Aff2, Aff3}, Chen, Minyan^{Aff1, Aff2, Aff3}, Zhang, Wenzhe^{Aff1, Aff2, Aff3}, Chen, Hanxi^{Aff1, Aff2, Aff3}, Nie, Qian^{Aff1, Aff2, Aff3}, Guo, Rongrong^{Aff1, Aff2, Aff3}, Guo, Wenhui^{Aff1, Aff2, Aff3, IDs13062024004812_cor13}, Fu, Fangmeng^{Aff1, Aff2, Aff3, IDs13062024004812_cor14}, Wang, Chuan^{Aff1, Aff2, Aff3, IDs13062024004812_cor15}

المصدر: Biology Direct. 19(1)

المؤلفون: Jagyeong Oh, Davide Pradella, Changwei Shao, Hairi Li, Namjeong Choi, Jiyeon Ha, Sonia Ruggiero, Xiang-Dong Fu, Xuexiu Zheng, Claudia Ghigna, Haihong Shen

المصدر: Cells, Vol 10, Iss 4, p 858 (2021)

مصطلحات موضوعية: alternative splicing, breast cancer, exon skipping, cancer metastasis, DCUN1D5, Cytology, QH573-671

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2073-4409/10/4/858; https://doaj.org/toc/2073-4409

URL الوصول: https://doaj.org/article/0e25bcbfa710456fafb43b35e31eb1ef

المؤلفون: Namjeong Choi, Jiyeon Ha, Jagyeong Oh, Changwei Shao, Claudia Ghigna, Xiang-Dong Fu, Haihong Shen, Davide Pradella, Sonia Ruggiero, Hairi Li, Xuexiu Zheng

المصدر: Cells
Cells, Vol 10, Iss 858, p 858 (2021)
Cells, vol 10, iss 4
Volume 10
Issue 4

مصطلحات موضوعية: DCUN1D5, Messenger, Breast Neoplasms, Biology, Article, Metastasis, Cell Line, Exon, alternative splicing, Breast cancer, breast cancer, cancer metastasis, Cell Line, Tumor, medicine, Genetics, RNA Precursors, 2.1 Biological and endogenous factors, Humans, RNA, Messenger, Aetiology, Peptide Synthases, lcsh:QH301-705.5, Cancer, Oncogene Proteins, Neoplastic, Tumor, Base Sequence, Serine-Arginine Splicing Factors, Alternative splicing, Reproducibility of Results, General Medicine, Exons, medicine.disease, Metastatic breast cancer, Survival Analysis, Exon skipping, Nonsense Mediated mRNA Decay, Gene Expression Regulation, Neoplastic, Alternative Splicing, Gene Expression Regulation, lcsh:Biology (General), RNA splicing, Cancer research, RNA, Female, Biotechnology, exon skipping

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41b77f820c0e10ee7c5d3bf30c16d2ec
https://pubmed.ncbi.nlm.nih.gov/33918758

المؤلفون: Gian Paolo Tonini, Maria Capasso, Raffaella Defferrari, Maria Antonietta Tufano, Lucio Nitsch, Tommy Martinsson, Katia Mazzocco, Annalisa Passariello, Roberta Migliorati, Daniele De Brasi, Paolo Siani, Rita Genesio

المساهمون: Passariello, Annalisa, De Brasi, D, Defferrari, R, Genesio, R, Tufano, M, Mazzocco, K, Capasso, M, Migliorati, Roberta, Martinsson, T, Siani, P, Nitsch, Lucio, Tonini, Gp

المصدر: European journal of medical genetics. 56(11)

مصطلحات موضوعية: SLE, domain containing 5, Gene Dosage, European cytogeneticists association register of unbalanced chromosome aberration, Germline, Loss of heterozygosity, Neuroblastoma, pseudo autosomal region 1, systemic lupus erythematosus, MYCN, DECIPHER, Jacobsen syndrome, multiplex ligation-dependent probe amplification, 11q syndrome, Genetics (clinical), Genetics, Oncogene Proteins, N-Myc Proto-Oncogene Protein, 123-iodine metaidobenzoguadinyl scintigrafy, database of genomic variant, MMP, medicine.diagnostic_test, Brain Neoplasms, MMP13, Nuclear Proteins, General Medicine, Syndrome, matrix metalloproteinase gene, DGV, PAR1, MLPA, International NB Staging System, structural copy number variation, ECARUCA, GYG2, array comparative genomic hybridization, Female, INSS, ARSD, matrix metalloproteinase 13, Chromosome Deletion, ARSE, CR, ARSH, DCUN1D5, CNV, Trigonocephaly, Biology, Craniosynostoses, FISH, aCGH, Hypotelorism, critical region, medicine, MCA/MR, Humans, Abnormalities, Multiple, DCN1, Multiplex ligation-dependent probe amplification, fluorescence in situ hybridization, Oncogene, Germ-Line Mutation, Chromosomes, Human, Pair 11, database of chromosomal imbalance and phenotype in humans using ensembl resource, Infant, arilsulphatases gene, multiple congenital anomaly/mental retardation, medicine.disease, (123)MIBG, defective in cullin neddylation 1, Cancer research, NB, glycogenin 2 gene, Fluorescence in situ hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3d103735750a021ada53799c84d40c2
https://pubmed.ncbi.nlm.nih.gov/24035971

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المؤلفون: Passariello A; Department of Medical Translational Sciences, University of Naples 'Federico II', Naples, Italy; Neonatology Unit, AORN dei Colli - V. Monaldi Hospital, Naples, Italy. Electronic address: annalisa.passariello@unina.it., De Brasi D, Defferrari R, Genesio R, Tufano M, Mazzocco K, Capasso M, Migliorati R, Martinsson T, Siani P, Nitsch L, Tonini GP

المصدر: European journal of medical genetics [Eur J Med Genet] 2013 Nov; Vol. 56 (11), pp. 626-34. Date of Electronic Publication: 2013 Sep 13.

نوع المنشور: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Chromosome Deletion*, Abnormalities, Multiple/*genetics , Brain Neoplasms/*genetics , Chromosomes, Human, Pair 11/*genetics , Craniosynostoses/*genetics , Neuroblastoma/*genetics , Nuclear Proteins/*genetics , Oncogene Proteins/*genetics, Abnormalities, Multiple/diagnosis ; Brain Neoplasms/congenital ; Brain Neoplasms/diagnosis ; Craniosynostoses/diagnosis ; Female ; Gene Dosage ; Germ-Line Mutation ; Humans ; Infant ; N-Myc Proto-Oncogene Protein ; Neuroblastoma/congenital ; Neuroblastoma/diagnosis ; Syndrome