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1دورية أكاديمية
المؤلفون: Eri Narukami, Takashi Anayama, Marino Yamamoto, Yujiro Bunno, Ryohei Miyazaki, Hironobu Okada, Mitsuko Iguchi
المصدر: Thoracic Cancer, Vol 14, Iss 23, Pp 2314-2319 (2023)
مصطلحات موضوعية: chest wall tumor, FUS gene translocation, LGFMS, pulmonary invasion, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Yagiz Alp Aksoy, Alexander J Cole, Wei Deng, Daniel Hesselson
المصدر: Cells, Vol 13, Iss 5, p 372 (2024)
مصطلحات موضوعية: Amyotrophic Lateral Sclerosis (ALS), CCNF gene, FUS gene, Zebrafish models, CRISPR/Cas9 genome editing, TALEN-mediated genome editing, Cytology, QH573-671
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Hirofumi Yamashita, Hodaka Yamakado, Makoto Urushitani, Nobukatsu Sawamoto, Ryosuke Takahashi, Ryota Hikiami, Shinsui Tatsumi, Takashi Ayaki, Teruyuki Tsuji, Yuichiro Hashi
المصدر: Internal Medicine. 2018, 57(13):1917
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4دورية أكاديمية
المؤلفون: Ruiz, J. A., Bernar, E. M., Jung, K.
المصدر: Plos One ; Vol.10, no.1 ; e0117040 ; http://www.plosone.org/home.actionTest
مصطلحات موضوعية: ZINC ION, WILD TYPE, UNCLASSIFIED DRUG, SPECTROPHOTOMETRY, SIDEROPHORE, RHIZOBIALES, PYOVERDINE, PSEUDOMONAS PROTEGENS, PSEUDOMONAS FLUORESCENS GROUP, PSEUDOMONAS, PROTEIN EXPRESSION, NONHUMAN, MULTIDRUG RESISTANCE PROTEIN, MINIMUM INHIBITORY CONCENTRATION, MICROBIAL PRODUCTS NOT CLASSIFIED ELSEWHERE, MANGANESE, GROWTH INHIBITION, GENE EXPRESSION, FUSARIUM, FUSARIC ACID, FUS GENE, FUNGI, FERROUS ION, FERRIC ION, ENANTIO PYOCHELIN, DRUG BINDING, COPPER ION, CONTROLLED STUDY, CONCENTRATION RESPONSE, CELL MOTILITY
وصف الملف: application/pdf
الإتاحة: https://doi.org/10.1371/journal.pone.0117040Test
http://ri.agro.uba.ar/greenstone3/library/collection/arti/document/2015ruizTest -
5دورية أكاديميةRecombination of chl-fus gene (Plastid Origin) downstream of hop: a locus of chromosomal instability
المساهمون: Laboratorio de Biología Molecular, Escuela de Biología, Universidad Industrial de Santander, Universidad Industrial de Santander Bucaramanga (UIS), Institut de minéralogie, de physique des matériaux et de cosmochimie (IMPMC), Muséum national d'Histoire naturelle (MNHN)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de recherche pour le développement IRD : UR206-Centre National de la Recherche Scientifique (CNRS)
المصدر: ISSN: 1471-2164 ; BMC Genomics ; https://hal.sorbonne-universite.fr/hal-01212972Test ; BMC Genomics, 2015, 16, pp.573. ⟨10.1186/s12864-015-1780-1⟩.
مصطلحات موضوعية: TPR proteins, hop gene, cEF-G, chl-fus gene, Microsynteny, Exon shuffling, Intron phase, [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology
العلاقة: hal-01212972; https://hal.sorbonne-universite.fr/hal-01212972Test; https://hal.sorbonne-universite.fr/hal-01212972/documentTest; https://hal.sorbonne-universite.fr/hal-01212972/file/s12864-015-1780-1.pdfTest
الإتاحة: https://doi.org/10.1186/s12864-015-1780-1Test
https://hal.sorbonne-universite.fr/hal-01212972Test
https://hal.sorbonne-universite.fr/hal-01212972/documentTest
https://hal.sorbonne-universite.fr/hal-01212972/file/s12864-015-1780-1.pdfTest -
6دورية أكاديمية
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7دورية أكاديمية
المؤلفون: Lanteri P., Meola I., Canosa A., De Marco G., Lomartire A., Rinaudo M. T., Albamonte E., Sansone V. A., Lunetta C., Manera U., Vasta R., Moglia C., Calvo A., Origone P., Chio A., Mandich P.
المساهمون: Lanteri P., Meola I., Canosa A., De Marco G., Lomartire A., Rinaudo M.T., Albamonte E., Sansone V.A., Lunetta C., Manera U., Vasta R., Moglia C., Calvo A., Origone P., Chio A., Mandich P.
مصطلحات موضوعية: FUS gene, Juvenile amyotrophic lateral sclerosi, Truncated FUS protein expression
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33637330; info:eu-repo/semantics/altIdentifier/wos/MEDLINE:33637330; firstpage:1; lastpage:4; numberofpages:4; journal:NEUROBIOLOGY OF AGING; http://hdl.handle.net/2318/1778138Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85101375527
الإتاحة: https://doi.org/10.1016/j.neurobiolaging.2021.01.029Test
http://hdl.handle.net/2318/1778138Test -
8دورية أكاديمية
المساهمون: Başak, Ayşe Nazlı (ORCID 0000-0001-9257-3540 & YÖK ID 1512), Bodur, Muhittin, Toker, Rabia Tütüncü, Okan, Mehmet Sait, Koç University Research Center for Translational Medicine (KUTTAM) / Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM), School of Medicine
المصدر: Turkish Journal of Pediatrics
مصطلحات موضوعية: Pediatrics, Juvenile amyotrophic lateral sclerosis, FUS gene
وصف الملف: text/academic publication
العلاقة: Publisher version; Koç University Institutional Repository; Bodur, Muhittin, Rabia T. Toker, Ayse N. Basak, and Mehmet S. Okan. ""A Rare Case of Juvenile Amyotrophic Lateral Sclerosis."" The Turkish Journal of Pediatrics. 63.3 (2021): 495-499.; https://dx.doi.org/10.24953/turkjped.2021.03.017Test; IR03035.pdf; WoS; Scopus; PubMed; NA; http://libdigitalcollections.ku.edu.tr/cdm/ref/collection/IR/id/9692Test
الإتاحة: https://doi.org/10.24953/turkjped.2021.03.017Test
http://libdigitalcollections.ku.edu.tr/cdm/ref/collection/IR/id/9692Test -
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المؤلفون: Irene Meola, Maria Teresa Rinaudo, Giovanni de Marco, Christian Lunetta, Paola Origone, Emilio Albamonte, Adriano Chiò, Cristina Moglia, Paola Mandich, Valeria A. Sansone, Annarosa Lomartire, Rosario Vasta, Antonio Canosa, Andrea Calvo, Umberto Manera, Paola Lanteri
مصطلحات موضوعية: 0301 basic medicine, Proband, Aging, medicine.medical_specialty, Heterozygote, Juvenile amyotrophic lateral sclerosis, Gene Expression, Loss of Heterozygosity, Gene mutation, medicine.disease_cause, FUS gene, 03 medical and health sciences, Exon, 0302 clinical medicine, Internal medicine, medicine, Humans, Cognitive Dysfunction, RNA, Messenger, Truncated FUS protein expression, Child, Genetic Association Studies, Mutation, biology, business.industry, General Neuroscience, Amyotrophic Lateral Sclerosis, Wild type, Exons, 030104 developmental biology, Endocrinology, biology.protein, Disease Progression, RNA-Binding Protein FUS, Female, Neurology (clinical), Geriatrics and Gerontology, Antibody, business, 030217 neurology & neurosurgery, Nuclear localization sequence, Developmental Biology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10c9399758a8ee88ea463149dac02123Test
http://hdl.handle.net/2318/1778138Test -
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المؤلفون: Rabia Tütüncü Toker, Mehmet Okan, Muhittin Bodur, Ayşe Nazlı Başak
المساهمون: Başak, Ayşe Nazlı (ORCID 0000-0001-9257-3540 & YÖK ID 1512), Bodur, Muhittin, Toker, Rabia Tütüncü, Okan, Mehmet Sait, Koç University Research Center for Translational Medicine (KUTTAM) / Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM), School of Medicine
المصدر: Turkish Journal of Pediatrics
مصطلحات موضوعية: Mutation, Weakness, Pathology, medicine.medical_specialty, business.industry, Juvenile amyotrophic lateral sclerosis, Disease, Motor neuron, FUS gene, medicine.disease, medicine.disease_cause, Pediatrics, medicine.anatomical_structure, Pediatrics, Perinatology and Child Health, Rare case, Medicine, Sarcoma, Amyotrophic lateral sclerosis, medicine.symptom, business
وصف الملف: text/academic publication
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca02750aa8730e15c21823a090614654Test
http://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/9692Test