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1دورية أكاديمية
المؤلفون: Behrendt-Møller, Ida, Stoltze, Ulrik, Hjalgrim, Lisa Lyngsie, Hansen, Thomas van Overeem, Schmiegelow, Kjeld, Wadt, Karin
المصدر: Behrendt-Møller , I , Stoltze , U , Hjalgrim , L L , Hansen , T V O , Schmiegelow , K & Wadt , K 2021 , ' Genomforskningsprojekt påviser TP53-mutation hos en pige med rabdomyosarkom ' , Ugeskrift for Laeger , bind 183 , nr. 32 . < https://content.ugeskriftet.dk/sites/default/files/scientific_article_files/2021-07/v03210228_web.pdfTest >
مصطلحات موضوعية: Child, Preschool, Female, Genes, p53/genetics, Genetic Predisposition to Disease, Germ-Line Mutation, Humans, Li-Fraumeni Syndrome/genetics, Pedigree, Rhabdomyosarcoma/genetics
وصف الملف: application/pdf
الإتاحة: https://curis.ku.dk/portal/da/publications/genomforskningsprojekt-paaviser-tp53mutation-hos-en-pige-med-rabdomyosarkomTest(eb1cda46-6e49-4096-a987-a7718e5384c8).html
https://curis.ku.dk/ws/files/337348261/v03210228_web.pdfTest
https://content.ugeskriftet.dk/sites/default/files/scientific_article_files/2021-07/v03210228_web.pdfTest -
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المؤلفون: Hiroshi Nanjyo, Hiroyuki Shibata, Taichi Yoshida, Daiki Taguchi, Koji Fukuda, Kazuhiro Shimazu, Shodai Takahashi, Tsutomu Takahashi, Koya Kodama
المصدر: Japanese Journal of Clinical Oncology. 50:1214-1217
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Cancer Research, Lung Neoplasms, Adenocarcinoma of Lung, Bone Neoplasms, Li-Fraumeni Syndrome, 03 medical and health sciences, T790M, 0302 clinical medicine, Germline mutation, Gefitinib, Epidermal growth factor, medicine, Humans, Radiology, Nuclear Medicine and imaging, Osimertinib, Protein Kinase Inhibitors, Germ-Line Mutation, Acrylamides, Aniline Compounds, business.industry, Bone metastasis, General Medicine, medicine.disease, Pedigree, respiratory tract diseases, 030104 developmental biology, Oncology, Li–Fraumeni syndrome, 030220 oncology & carcinogenesis, Cancer research, Adenocarcinoma, Female, Tumor Suppressor Protein p53, business, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69c47a46ee64a2225ecf59e29bc2f69aTest
https://doi.org/10.1093/jjco/hyaa095Test -
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المؤلفون: Keishiro Amano, Mami Takeoka, Masahiro Hirayama, Ryo Hanaki, Naofumi Suzuki, Junya Hirayama, Shotaro Iwamoto, Hidemi Toyoda
المصدر: Journal of Pediatric Hematology/Oncology. 43:e567-e570
مصطلحات موضوعية: Male, Oncology, medicine.medical_specialty, Malignancy, Li-Fraumeni Syndrome, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, Internal medicine, Rhabdomyosarcoma, Cancer screening, Adrenocortical Carcinoma, medicine, Humans, Missense mutation, Adrenocortical carcinoma, Genetic Predisposition to Disease, Child, Germ-Line Mutation, business.industry, Cancer, Hematology, medicine.disease, Adrenal Cortex Neoplasms, Pedigree, Li–Fraumeni syndrome, Child, Preschool, 030220 oncology & carcinogenesis, Pediatrics, Perinatology and Child Health, Tumor Suppressor Protein p53, business, 030215 immunology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::babe29e47458c83cf265961a94e9a14bTest
https://doi.org/10.1097/mph.0000000000001862Test -
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المؤلفون: John G. Aversa, Liqiang Xi, Sho Yano, Donald W. Hadley, Naris Nilubol, Irini Manoli, Mark Raffeld, Samira M. Sadowski, Francine Blumental De Abreu
المصدر: BMC Cancer, Vol 20, Iss 1, Pp 1-6 (2020)
BMC Cancerمصطلحات موضوعية: Adult, 0301 basic medicine, Oncology, Heterozygote, Cancer Research, medicine.medical_specialty, Genotype, Genetic counseling, Case Report, Neuroendocrine tumors, lcsh:RC254-282, Loss of heterozygosity, 03 medical and health sciences, Hereditary pancreatic neoplasm, 0302 clinical medicine, Surgical oncology, Pancreatic neuroendocrine tumor, Internal medicine, Pancreatic cancer, Genetics, medicine, Humans, Genetic Predisposition to Disease, Li-Fraumeni syndrome, TP53, neoplasms, Germ-Line Mutation, business.industry, Astrocytoma, Genes, p53, medicine.disease, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Choroid plexus papilloma, Pedigree, Pancreatic Neoplasms, Neuroendocrine Tumors, 030104 developmental biology, Li–Fraumeni syndrome, 030220 oncology & carcinogenesis, Female, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a7ad87b3827327686f3d3df8401244fTest
http://link.springer.com/article/10.1186/s12885-020-06723-6Test -
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المؤلفون: Louise C. Strong, Christopher I. Amos, Elissa B. Dodd-Eaton, Jingxiao Chen, Wenyi Wang, Jing Ning, Jasmina Bojadzieva, Fan Gao, Xianhua Kong, Seung Jun Shin
المصدر: Cancer Res
مصطلحات موضوعية: Male, 0301 basic medicine, Oncology, Cancer Research, Time Factors, Datasets as Topic, Penetrance, Li-Fraumeni Syndrome, 0302 clinical medicine, Mutation Rate, Child, Neoplasms, Second Primary, Second primary cancer, Middle Aged, Pedigree, Child, Preschool, 030220 oncology & carcinogenesis, Cohort, Female, Adult, Heterozygote, medicine.medical_specialty, Adolescent, Genetic counseling, Genetic Counseling, Risk Assessment, Article, Young Adult, 03 medical and health sciences, Germline mutation, Predictive Value of Tests, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Germ-Line Mutation, Models, Genetic, business.industry, Infant, Newborn, Computational Biology, Infant, Cancer, medicine.disease, Confidence interval, 030104 developmental biology, Li–Fraumeni syndrome, Tumor Suppressor Protein p53, business, Software, Follow-Up Studies
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4879382bc2bbe4b8656d95cdd290b37Test
https://doi.org/10.1158/0008-5472.can-19-0725Test -
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المؤلفون: Ida, Behrendt-Møller, Ulrik, Stoltze, Lisa Lyngsie, Hjalgrim, Thomas van Overeem, Hansen, Kjeld, Schmiegelow, Karin, Wadt
المصدر: Ugeskrift for laeger. 183(32)
مصطلحات موضوعية: Li-Fraumeni Syndrome, Child, Preschool, Rhabdomyosarcoma, Humans, Female, Genetic Predisposition to Disease, Child, Genes, p53, Germ-Line Mutation, Pedigree
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::593d610cf773da0a95c60b09d5ffe803Test
https://pubmed.ncbi.nlm.nih.gov/34378529Test -
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المؤلفون: Behrendt-Møller, Ida, Stoltze, Ulrik, Hjalgrim, Lisa Lyngsie, Hansen, Thomas van Overeem, Schmiegelow, Kjeld, Wadt, Karin
المصدر: Behrendt-Møller, I, Stoltze, U, Hjalgrim, L L, Hansen, T V O, Schmiegelow, K & Wadt, K 2021, ' Genomforskningsprojekt påviser TP53-mutation hos en pige med rabdomyosarkom ', Ugeskrift for Laeger, bind 183, nr. 32 . < https://content.ugeskriftet.dk/sites/default/files/scientific_article_files/2021-07/v03210228_web.pdfTest >
مصطلحات موضوعية: Genes, p53/genetics, Rhabdomyosarcoma/genetics, Child, Preschool, Humans, Female, Genetic Predisposition to Disease, Child, Germ-Line Mutation, Li-Fraumeni Syndrome/genetics, Pedigree
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od______2751::845925cd25dfce53db6902c08020422cTest
https://curis.ku.dk/portal/da/publications/genomforskningsprojekt-paaviser-tp53mutation-hos-en-pige-med-rabdomyosarkomTest(eb1cda46-6e49-4096-a987-a7718e5384c8).html -
8دورية أكاديمية
المساهمون: Yonggeun Cho, Juwon Kim, Yoonjung Kim, Joon Jeong, Kyung-A Lee, Kim, Yoon Jung, Kim, Ju Won, Lee, Kyung A, Jeong, Joon
المصدر: T201301734.pdf
مصطلحات موضوعية: Adolescent, Adult, Breast Neoplasms/complications, Breast Neoplasms/diagnosis, Breast Neoplasms/therapy, Combined Modality Therapy, Exons, Female, Genotype, Heterozygote, Humans, Li-Fraumeni Syndrome/complications, Li-Fraumeni Syndrome/diagnosis, Li-Fraumeni Syndrome/therapy, Middle Aged, Multimodal Imaging, Mutation, Missense, Pedigree, Sequence Analysis, DNA, Tumor Suppressor Protein p53/genetics, Young Adult, Breast cancer, LFL, LFS, Late onset, Li-Fraumeni syndrome, Li-Fraumeni-like syndrome, Penetrance
وصف الملف: application/pdf
العلاقة: ANNALS OF LABORATORY MEDICINE; J00164; OAK-2013-00911; https://ir.ymlib.yonsei.ac.kr/handle/22282913/87029Test; T201301734; ANNALS OF LABORATORY MEDICINE, Vol.33(3) : 212-216, 2013
الإتاحة: https://doi.org/10.3343/alm.2013.33.3.212Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/87029Test -
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المؤلفون: Jianfeng Zhou, Haiyun An, Jia Gu, Di Wang, Xiaolu Long, Li Zhu, Yaoyao Lou, Yi Xiao, Yang Cao, Ying Wang, Na Wang, Jin Wang, Min Xiao, Liting Chen, Gaoxiang Wang, Chunrui Li, Bin Xu
المصدر: Journal for ImmunoTherapy of Cancer, Vol 8, Iss 1 (2020)
Journal for Immunotherapy of Cancerمصطلحات موضوعية: Adult, Male, 0301 basic medicine, Oncology, Cancer Research, medicine.medical_specialty, Immunology, Case Report, Gene mutation, Immunotherapy, Adoptive, Li-Fraumeni Syndrome, 03 medical and health sciences, 0302 clinical medicine, Precursor B-Cell Lymphoblastic Leukemia-Lymphoma, Internal medicine, medicine, Humans, Immunology and Allergy, RC254-282, Salvage Therapy, Pharmacology, business.industry, Lymphoblastic lymphoma, Cancer, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Prognosis, medicine.disease, Minimal residual disease, Pedigree, Transplantation, Cytokine release syndrome, 030104 developmental biology, Drug Resistance, Neoplasm, Li–Fraumeni syndrome, 030220 oncology & carcinogenesis, Acute Disease, Mutation, Monoclonal, haematology, Molecular Medicine, Female, immunotherapy, Neoplasm Recurrence, Local, Tumor Suppressor Protein p53, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::360ff6d4d80517742f365b5701085dcbTest
https://jitc.bmj.com/content/8/1/e000364.fullTest -
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المؤلفون: Nuno Coimbra, Manuel R. Teixeira, Carla Escudeiro, Marco Ferreira, Joana Guerra, Pedro Pinto, Joana Vieira, Rui Santos, Catarina Santos, Ana Berta Sousa, Ana Peixoto, Manuela Pinheiro, Paula Lopes, C. Leal, Carla M. A. Pinto, João Silva, Susana Lisboa
المصدر: Familial cancer. 20(3)
مصطلحات موضوعية: 0301 basic medicine, Oncology, Adult, Cancer Research, medicine.medical_specialty, Breast Neoplasms, 030105 genetics & heredity, Germline, Li-Fraumeni Syndrome, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, Breast cancer, Internal medicine, Epidemiology, Genetics, medicine, Humans, Genetic Predisposition to Disease, First-degree relatives, skin and connective tissue diseases, neoplasms, Genetics (clinical), Germ-Line Mutation, In Situ Hybridization, Fluorescence, Sanger sequencing, business.industry, Carcinoma, Ductal, Breast, Age Factors, Gene Amplification, Cancer, High-Throughput Nucleotide Sequencing, Sequence Analysis, DNA, Genes, erbB-2, medicine.disease, Genes, p53, Pedigree, Li–Fraumeni syndrome, 030220 oncology & carcinogenesis, symbols, Female, Breast carcinoma, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::930f2af97a7995afe1014e782285d9c3Test
https://pubmed.ncbi.nlm.nih.gov/33051812Test