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المؤلفون: Anna Marchesiello, Nevena Skroza, Concetta Potenza, Vincenzo Petrozza, Alessandra Mambrin, Ersilia Tolino, Ilaria Proietti, Alessia Anzalone, Nicoletta Bernardini, Natale Porta
مصطلحات موضوعية: medicine.medical_specialty, chromosomes, Dermatology, Disease, pair 1, 030207 dermatology & venereal diseases, 03 medical and health sciences, 0302 clinical medicine, Intellectual disability, medicine, Hidradenitis suppurativa, Abnormalities, Multiple, 030212 general & internal medicine, human, humans, trisomy, Groin, Chromosomes, Human, Pair 13, business.industry, adult, Apocrine, hidradenitis suppurativa, abnormalities, multiple, chromosomes, human, pair 13, female, chromosomes, human, pair 1, medicine.disease, Perineum, body regions, multiple, pair 13, Infectious Diseases, medicine.anatomical_structure, Chromosomes, Human, Pair 1, abnormalities, Metabolic syndrome, business, Trisomy
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c660d41807956328b013be5c053951dTest
http://hdl.handle.net/11573/1393233Test -
2دورية أكاديمية
المؤلفون: Skroza N., Mambrin A., Tolino E., Bernardini N., Proietti I., Anzalone A., Marchesiello A., Porta N., Petrozza V., Potenza C.
المساهمون: Skroza, N., Mambrin, A., Tolino, E., Bernardini, N., Proietti, I., Anzalone, A., Marchesiello, A., Porta, N., Petrozza, V., Potenza, C.
مصطلحات موضوعية: abnormalities, multiple, adult, chromosomes, human, pair 13, female, hidradenitis suppurativa, pair 1, trisomy
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31535764; info:eu-repo/semantics/altIdentifier/wos/WOS:000487093200009; volume:33; issue:Suppl 6; firstpage:32; lastpage:33; numberofpages:2; journal:JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY; http://hdl.handle.net/11573/1393233Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85072398303
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المؤلفون: Yukiko Tsunematsu, Yasuo Horikoshi, Yasuhiko Kaneko, Haruhiko Eguchi, Hirofumi Kobayashi, Yoshihiro Komada, Atsushi Kikuta, Yoshiro Hatae, Takeshi Namiki, Jun Miyauchi, Kazuko Kumon
المصدر: Japanese Journal of Cancer Research : Gann
مصطلحات موضوعية: Hepatoblastoma, Male, Cancer Research, medicine.medical_specialty, 2q gain, Gene Dosage, Antineoplastic Agents, Biology, Gene dosage, Article, FISH, Japan, medicine, Humans, In Situ Hybridization, Fluorescence, CGH, Chromosome Aberrations, Genome, medicine.diagnostic_test, Liver Neoplasms, Cytogenetics, Infant, Newborn, Chromosome, Infant, Nucleic Acid Hybridization, Karyotype, DNA, Neoplasm, medicine.disease, Molecular biology, Survival Rate, Oncology, Chromosomes, Human, Pair 1, Child, Preschool, Chromosomes, Human, Pair 2, Karyotyping, Chromosomal region, Chromosome abnormalities, Female, Fluorescence in situ hybridization, Comparative genomic hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::453e6eb56449bb5f0d4672b5c6964ef2Test
http://europepmc.org/articles/PMC5926834Test -
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المؤلفون: Setsuo Hirohashi, Teruko Takarabe, Hitoshi Tsuda, Takashi Fukutomi
المصدر: Japanese Journal of Cancer Research : Gann
مصطلحات موضوعية: Adult, Cancer Research, medicine.medical_specialty, Pathology, Mammary gland, Aneuploidy, Chromosomal translocation, Breast Neoplasms, Biology, Article, Translocation, Genetic, Body Mass Index, Breast cancer, Chromosome 16, medicine, Humans, Genetic Predisposition to Disease, Breast, In Situ Hybridization, Fluorescence, Hyperplasia of mammary gland, Aged, Aged, 80 and over, Chromosome Aberrations, Hyperplasia, Loss of chromosome 16, Cytogenetics, Age Factors, Cancer, Cancer etiology, Middle Aged, medicine.disease, medicine.anatomical_structure, Oncology, Chromosomes, Human, Pair 1, Female, Der(16)t(1, 16)/der(1, 16), Chromosome Deletion, Menopause, Chromosomes, Human, Pair 16
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98a59d236d9be394b0f1c788bf126d25Test
http://europepmc.org/articles/PMC5926417Test -
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المؤلفون: Yohji Fukuda, Issei Imoto, Zeng-Quan Yang, Masayuki Imamura, Yusuke Nakamura, Johji Inazawa, Teruo Amagasa, Atiphan Pimkhaokham, Yutaka Shimada, Naoki Kurihara
المصدر: Japanese Journal of Cancer Research : Gann
مصطلحات موضوعية: Cancer Research, medicine.medical_specialty, Esophageal Neoplasms, Chromosomal Proteins, Non-Histone, Gene Dosage, medicine, Comparative genomic hybridization (CGH), Tumor Cells, Cultured, Humans, Centromere protein F (CENPF), Centromere Protein F, In Situ Hybridization, Fluorescence, Chromosome Aberrations, Activating Transcription Factor 3, medicine.diagnostic_test, biology, Microfilament Proteins, CENPF, Cytogenetics, Gene Amplification, Chromosome, Nucleic Acid Hybridization, Amplicon, Blotting, Northern, Molecular biology, Blotting, Southern, Oncology, Epidermoid carcinoma, Human activating transcription factor 3 (ATF3), Chromosomes, Human, Pair 1, Esophageal squamous cell carcinoma (ESC), Cancer research, biology.protein, Carcinoma, Squamous Cell, Chromosome Deletion, Amplicon map, Chromosomes, Human, Pair 9, Rapid Communication, Fluorescence in situ hybridization, Comparative genomic hybridization, Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdffa7e127742457f12ce4bf034b4ba5Test
http://europepmc.org/articles/PMC5926289Test -
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المؤلفون: Yoshihiro Kurita, Tetsuro Kobayashi, Hiroki Kurahashi, Koji Takami, Isamu Nishisho, Shoichi Fujita, Takesada Mori, Shin-ichiro Takai, Eisei Shin
المصدر: Japanese Journal of Cancer Research : Gann
مصطلحات موضوعية: Cancer Research, Pathology, medicine.medical_specialty, Heterozygote, endocrine system diseases, Deletion map, Chromosomes, Human, Pair 22, Adrenal Gland Neoplasms, Multiple endocrine neoplasia type 2, Pheochromocytoma, Biology, Article, Loss of heterozygosity, Gene mapping, medicine, Humans, Deletion mapping, neoplasms, Chromosome, Chromosome Mapping, medicine.disease, Oncology, Genetic marker, Chromosomes, Human, Pair 1, Chromosome Arm, Cancer research, Chromosome Deletion, DNA Probes, Chromosome 22
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::295eb9a37c4717413a4a9f26b8b3d576Test
http://europepmc.org/articles/PMC5919302Test -
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المؤلفون: Hiroshi Takatera, Taisei Nomura, Hiroaki Itatani
المصدر: Japanese Journal of Cancer Research : Gann
مصطلحات موضوعية: Male, Cancer Research, endocrine system diseases, Cellular differentiation, Mice, SCID, Testicle, chemistry.chemical_compound, Mice, Tumor Cells, Cultured, Lymph node, Spermatozoa, Kidney Neoplasms, Isoenzymes, medicine.anatomical_structure, Oncology, Chromosomes, Human, Pair 1, Organ Specificity, Differentiation, Lymphatic Metastasis, LDH‐X (C4), Rapid Communication, Adult, medicine.medical_specialty, endocrine system, Transplantation, Heterologous, Mice, Nude, Scid‐nustr mouse, Dysgerminoma, Biology, Human seminoma, Isozyme, Testicular Neoplasms, Lactate dehydrogenase, Internal medicine, Seminoma cell line, medicine, Animals, Humans, Severe combined immunodeficiency, L-Lactate Dehydrogenase, urogenital system, Seminoma, Electrophoresis, Cellulose Acetate, medicine.disease, Endocrinology, chemistry, Chromosome Inversion, Cancer research, Lymph Nodes, Spermatogenesis, Neoplasm Transplantation
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d54a7dff5bbffcf77e5851ac268d7c7Test
http://europepmc.org/articles/PMC5919147Test -
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المؤلفون: Takeshi Sodeyama, Seiichi Usuda, Kendo Kiyosawa, Shuhei Yamada, Seiichi Furuta, Koji Yabu, Paul K. Nakane, Kiyoshi Furuta, Kaname Yoshizawa, Yoshiyuki Nakatsuji, Eiji Tanaka, Shuichi Kaneko
المصدر: Japanese Journal of Cancer Research : Gann
مصطلحات موضوعية: Male, Cancer Research, Carcinoma, Hepatocellular, Hepatitis C virus, Molecular Sequence Data, Chromosomes, Human, Pair 20, Hepacivirus, Biology, medicine.disease_cause, Polymerase Chain Reaction, Virus, Article, Culture Techniques, medicine, Carcinoma, Biomarkers, Tumor, Tumor Cells, Cultured, Humans, Key words, In Situ Hybridization, Aged, Aged, 80 and over, Gene Rearrangement, Base Sequence, Liver Neoplasms, Gene rearrangement, Hepatocellular carcinoma cell line, Oligonucleotides, Antisense, medicine.disease, Virology, digestive system diseases, HCV‐RNA, Kinetics, Microscopy, Electron, Oncology, Oligodeoxyribonucleotides, Cell culture, Chromosomes, Human, Pair 1, Hepatocellular carcinoma, Karyotyping, biology.protein, RNA, Viral, Antibody, Nested polymerase chain reaction, Cell Division, Chromosomes, Human, Pair 17
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2b2a97fddfc3e204e2ab78878168f9eTest
http://europepmc.org/articles/PMC5918961Test -
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المؤلفون: Angelika Erkwoh, Rolf Fimmers, Otmar D. Wiestler, Lutz Kirsch, Guido Reifenberger, Uwe Schlegel, Jörg Felsberg, Britta Blaschke, Johannes Schramm, Michael Sabel
المصدر: Brain Pathol
55. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie e.V. (DGNC), 1. Joint Meeting mit der Ungarischen Gesellschaft für Neurochirurgie; 20040425-20040428; Köln; DOCP 06.59 /20040423/مصطلحات موضوعية: Oncology, Adult, Male, medicine.medical_specialty, Pathology, Adolescent, medicine.medical_treatment, Oligodendroglioma, Loss of Heterozygosity, Biology, Astrocytoma, Polymerase Chain Reaction, Pathology and Forensic Medicine, Loss of heterozygosity, Internal medicine, medicine, Humans, Oligodendroglial Tumor, Child, Survival rate, neoplasms, Survival analysis, Aged, Aged, 80 and over, Chemotherapy, Brain Neoplasms, General Neuroscience, Chromosome, Middle Aged, medicine.disease, Prognosis, Survival Analysis, Survival Rate, ddc: 610, Chromosomes, Human, Pair 1, Chromosome Arm, Disease Progression, Female, Neurology (clinical), Research Article, Microsatellite Repeats
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16c06e94aa57b0b8832512d969bfe4dcTest
https://europepmc.org/articles/PMC8095961Test/ -
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المؤلفون: Jan Oosting, Ronald van Eijk, Sjoerd G. van Duinen, Mathilde Kouwenhove, Anne-Marie Cleton-Jansen, Remco Natté, Johan M. Kros, Paul H. C. Eilers
المساهمون: Virology, Neurology, Pathology
المصدر: Brain Pathol
Brain Pathology, 15(3), 192-197. Wiley-Blackwellمصطلحات موضوعية: musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, In situ hybridization, Biology, Polymerase Chain Reaction, Sensitivity and Specificity, Pathology and Forensic Medicine, law.invention, law, 1p Deletion, Humans, Oligodendroglial Tumor, Multiplex, Multiplex ligation-dependent probe amplification, Genotyping, Polymerase chain reaction, In Situ Hybridization, Fluorescence, Brain Neoplasms, General Neuroscience, Reproducibility of Results, Glioma, Molecular biology, Chromosomal Loss, Chromosomes, Human, Pair 1, Neurology (clinical), Chromosome Deletion, Chromosomes, Human, Pair 19, Nucleic Acid Amplification Techniques, CORRESPONDENCE: Letters to the Editor, Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b6276772ee771e63173a2990efc5da8Test
https://europepmc.org/articles/PMC8095888Test/