المؤلفون: Junichi Imanishi, Takanori Maeda, Sae Ujiro, Mayuka Masuda, Yuta Kusakabe, Makoto Takemoto, Wataru Fujimoto, Koji Kuroda, Soichiro Yamashita, Masamichi Iwasaki, Takahumi Todoroki, Masanori Okuda

المصدر: European heart journal. Acute cardiovascular care.

مصطلحات موضوعية: General Medicine, Cardiology and Cardiovascular Medicine, Critical Care and Intensive Care Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::189885ea8d592b29d7117aff7b0504a6
https://pubmed.ncbi.nlm.nih.gov/36548965

المؤلفون: Issei Imoto, Tomohiro Kohmoto, Katsutoshi Shoda, Sae Ujiro, Rizu Takahashi, Kiyoshi Masuda, Daisuke Ichikawa, Eigo Otsuji, Shoichiro Tange

المصدر: Gastric Cancer. 23:403-417

مصطلحات موضوعية: Male, Cancer Research, Apoptosis, 03 medical and health sciences, 0302 clinical medicine, Stomach Neoplasms, Surgical oncology, Transcription (biology), Intestinal Neoplasms, Biomarkers, Tumor, Tumor Cells, Cultured, Humans, Gene silencing, Medicine, Claudin, Gene, Aged, Cell Proliferation, YAP1, business.industry, Cell growth, Cell Cycle, Gastroenterology, General Medicine, Prognosis, Gene Expression Regulation, Neoplastic, Survival Rate, Oncology, Cell culture, Case-Control Studies, 030220 oncology & carcinogenesis, Claudins, Cancer research, Female, 030211 gastroenterology & hepatology, business, Follow-Up Studies

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4f2ac107e6e0a2eea7f186912db1622
https://doi.org/10.1007/s10120-019-01014-x

المؤلفون: Miki Watanabe, Yuji Fujita, Takuya Naruto, Hideaki Horikawa, Kiyoshi Masuda, Tomohiro Kohmoto, Sae Ujiro, Issei Imoto, Nana Okamoto

المصدر: American journal of medical genetics. Part A. 173(4)

مصطلحات موضوعية: 0301 basic medicine, DNA Copy Number Variations, Non-allelic homologous recombination, Copy number analysis, Limb Deformities, Congenital, Organic Anion Transporters, Biology, Homology (biology), 03 medical and health sciences, Asian People, Mesomelia, Genetics, medicine, Humans, Abnormalities, Multiple, Child, Homologous Recombination, Genetics (clinical), Genes, Dominant, Sequence Deletion, Base Sequence, Breakpoint, High-Throughput Nucleotide Sequencing, Synostosis, medicine.disease, Osteochondrodysplasia, 030104 developmental biology, Long Interspersed Nucleotide Elements, Female, Sulfotransferases, Homologous recombination, Chromosomes, Human, Pair 8

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0ed0f93aa824878dd3885d713dfd30b
https://pubmed.ncbi.nlm.nih.gov/28328141