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1دورية أكاديمية
المؤلفون: José Luis Garrido-Huarte, Josep Fita-Torró, Rosa Viana, Amparo Pascual-Ahuir, Markus Proft
المصدر: Frontiers in Microbiology, Vol 14 (2023)
مصطلحات موضوعية: SARS-CoV-2, Saccharomyces cerevisiae, autophagy, Ca2+ homeostasis, ORF3a, ORF7a, Microbiology, QR1-502
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Lisa G. Riley, Matthew M. Heeney, Joëlle Rudinger-Thirion, Magali Frugier, Dean R. Campagna, Ronghao Zhou, Gregory A. Hale, Lee M. Hilliard, Joel A. Kaplan, Janet L. Kwiatkowski, Colin A. Sieff, David P. Steensma, Alexander J. Rennings, Annet Simons, Nicolaas Schaap, Richard J. Roodenburg, Tjitske Kleefstra, Leonor Arenillas, Josep Fita-Torró, Rasha Ahmed, Miguel Abboud, Elie Bechara, Roula Farah, Rienk Y. J. Tamminga, Sylvia S. Bottomley, Mayka Sanchez, Gerwin Huls, Dorine W. Swinkels, John Christodoulou, Mark D. Fleming
المصدر: Haematologica, Vol 103, Iss 12 (2018)
مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Amparo Pascual-Ahuir, Josep Fita-Torró, Markus Proft
المصدر: International Journal of Molecular Sciences, Vol 21, Iss 21, p 8278 (2020)
مصطلحات موضوعية: gene expression, transcriptional activation, transcriptional memory, single-cell variability, reporter assays, stress adaptation, Biology (General), QH301-705.5, Chemistry, QD1-999
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Beatriz Cadenas, Josep Fita-Torró, Mar Bermúdez-Cortés, Inés Hernandez-Rodriguez, José Luis Fuster, María Esther Llinares, Ana María Galera, Julia Lee Romero, Santiago Pérez-Montero, Cristian Tornador, Mayka Sanchez
المصدر: Pharmaceuticals, Vol 12, Iss 1, p 17 (2019)
مصطلحات موضوعية: ferritin, hereditary hyperferritinemia, hereditary hypoferritinemia, iron metabolism, cataracts syndrome, neurodegenerative disease, Medicine, Pharmacy and materia medica, RS1-441
وصف الملف: electronic resource
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5
المساهمون: Ministerio de Ciencia e Innovación (España), Proft, Markus
مصطلحات موضوعية: Genetics, Molecular evolution, GAL3, Budding yeast, GAL1, Sugar utilization, GAL switch, Ecology, Evolution, Behavior and Systematics
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72d2fe46b4478610f419bb5781d9d9c8
http://hdl.handle.net/10261/330499 -
6SARS-CoV-2 accessory proteins ORF3a and ORF7a modulate autophagic flux and Ca2+ homeostasis in yeast
المؤلفون: José Luis Garrido-Huarte, Josep Fita-Torró, Rosa Viana, Amparo Pascual-Ahuir, Markus Proft
المساهمون: Agencia Estatal de Investigación (España), Ministerio de Ciencia, Innovación y Universidades (España), Generalitat Valenciana, Pascual-Ahuir, Amparo
مصطلحات موضوعية: SARS-CoV-2, ORF3a, Autophagy, Ca2+ homeostasis, ORF7a, Saccharomyces cerevisiae
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27e49d48e2c7dc4dd0bd424d04a2f5f0
http://hdl.handle.net/10261/307775 -
7
المؤلفون: Lee Hilliard, Joëlle Rudinger-Thirion, Alexander J. Rennings, Magali Frugier, Richard J. Roodenburg, Lisa G. Riley, Leonor Arenillas, David P. Steensma, Josep Fita-Torró, Elie Bechara, Mark D. Fleming, Sylvia S. Bottomley, Gregory A. Hale, Janet L. Kwiatkowski, Rienk Y. J. Tamminga, Ronghao Zhou, Dean R. Campagna, Joel Kaplan, Miguel R. Abboud, Matthew M. Heeney, Colin A. Sieff, Nicolaas Schaap, Rasha Ahmed, John Christodoulou, Dorine W. Swinkels, Gerwin Huls, Mayka Sanchez, Tjitske Kleefstra, Roula Farah, Annet Simons
المساهمون: Stem Cell Aging Leukemia and Lymphoma (SALL), Guided Treatment in Optimal Selected Cancer Patients (GUTS), Genetic Metabolic Disorders Research Unit, Westmead Hospital [Sydney]-Kids Research Institute, Architecture et Réactivité de l'ARN (ARN), Institut de biologie moléculaire et cellulaire (IBMC), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS), St Jude Children's Research Hospital, 849 Department of Human Genetics, Radboud University Medical Center [Nijmegen], Balamand University Medical School, Westmead Hospital [Sydney]
المصدر: Haematologica
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Haematologica, 103(12), 2008-2015. FERRATA STORTI FOUNDATION
Haematologica, 103, 2008-2015
Haematologica, Ferrata Storti Foundation, 2018, 103 (12), pp.2008-2015. ⟨10.3324/haematol.2017.182659⟩
Haematologica, 103, 12, pp. 2008-2015مصطلحات موضوعية: 0301 basic medicine, Anemia, [SDV]Life Sciences [q-bio], Anèmia, TRANSFER-RNA SYNTHETASE, Biology, 03 medical and health sciences, All institutes and research themes of the Radboud University Medical Center, Germline mutation, Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience [Radboudumc 7], Sideroblastic anemia, Mitochondrial myopathy, medicine, Missense mutation, HETEROGENEITY, Allele, MUTATION, Exome sequencing, ComputingMilieux_MISCELLANEOUS, Genetics, IDENTIFICATION, Cancer development and immune defence RIHS: Radboud Institute for Health Sciences [Radboudumc 2], Hematology, medicine.disease, Renal disorders RIMLS: Radboud Institute for Molecular Life Sciences [Radboudumc 11], 3. Good health, Fenotip, Cancer development and immune defence RIMLS: Radboud Institute for Molecular Life Sciences [Radboudumc 2], Mitochondrial diseases RIMLS: Radboud Institute for Molecular Life Sciences [Radboudumc 6], 030104 developmental biology, Lactic acidosis
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e33db39b676f24e3649b6850f1684f6a
https://doi.org/10.3324/haematol.2017.182659 -
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المؤلفون: Josep Fita-Torró, Markus Proft, Amparo Pascual-Ahuir
المساهمون: Ministerio de Ciencia, Innovación y Universidades (España), Proft, Markus, Proft, Markus [0000-0002-6788-5830]
المصدر: International Journal of Molecular Sciences, Vol 21, Iss 8278, p 8278 (2020)
Digital.CSIC. Repositorio Institucional del CSIC
instname
International Journal of Molecular Sciences
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valénciaمصطلحات موضوعية: Cell physiology, Yeast Model, Transcription, Genetic, Living cell, Computational biology, Review, Biology, Catalysis, Transcriptional dynamics, Cell Physiological Phenomena, Inorganic Chemistry, lcsh:Chemistry, Genetic Heterogeneity, Transcriptional memory, Transcriptional activation, Gene expression, BIOQUIMICA Y BIOLOGIA MOLECULAR, Animals, Humans, Physical and Theoretical Chemistry, Stress adaptation, Molecular Biology, lcsh:QH301-705.5, Spectroscopy, Regulation of gene expression, Organic Chemistry, Dynamics (mechanics), Single-cell variability, Gene Expression Regulation, Developmental, General Medicine, Computer Science Applications, Chromatin, Molecular Imaging, lcsh:Biology (General), lcsh:QD1-999, Single-Cell Analysis, Reporter assays
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d188f23d330ce4f9d7dc75a8470023b1
https://hdl.handle.net/10251/169418 -
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المؤلفون: Carlos Andrés Martínez-Garay, Carlos García-Ferris, María Teresa Martínez-Pastor, Isabel Mulet, Antonia María Romero, Sergi Puig, Lucía Ramos-Alonso, Josep Fita-Torró, María Jesús Lozano, Nadine Wittmaack
المساهمون: Ministerio de Economía y Competitividad (España), Ministerio de Economía, Industria y Competitividad (España), European Commission
المصدر: Digital.CSIC. Repositorio Institucional del CSIC
instnameمصطلحات موضوعية: 0301 basic medicine, Saccharomyces cerevisiae Proteins, Transcription, Genetic, Iron, Saccharomyces cerevisiae, Biophysics, Biochemistry, Cofactor, Biomaterials, 03 medical and health sciences, Fet3, Gene Expression Regulation, Fungal, Cth2, medicine, Baker’s yeast, Ypk1, Transcription factor, Alleles, chemistry.chemical_classification, Reactive oxygen species, biology, Kinase, Iron deficiency, Respiration, Metals and Alloys, biology.organism_classification, medicine.disease, Yeast, Cell biology, Iron toxicity, 030104 developmental biology, chemistry, Iron-deficiency anemia, Chemistry (miscellaneous), biology.protein, Aft1
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea85dc68855b23778d33dca61f16da7f
https://pubmed.ncbi.nlm.nih.gov/30137082 -
10
المؤلفون: Lisa G, Riley, Matthew M, Heeney, Joëlle, Rudinger-Thirion, Magali, Frugier, Dean R, Campagna, Ronghao, Zhou, Gregory A, Hale, Lee M, Hilliard, Joel A, Kaplan, Janet L, Kwiatkowski, Colin A, Sieff, David P, Steensma, Alexander J, Rennings, Annet, Simons, Nicolaas, Schaap, Richard J, Roodenburg, Tjitske, Kleefstra, Leonor, Arenillas, Josep, Fita-Torró, Rasha, Ahmed, Miguel, Abboud, Elie, Bechara, Roula, Farah, Rienk Y J, Tamminga, Sylvia S, Bottomley, Mayka, Sanchez, Gerwin, Huls, Dorine W, Swinkels, John, Christodoulou, Mark D, Fleming
المصدر: Haematologica
مصطلحات موضوعية: Male, Adolescent, Mutation, Missense, Infant, Genetic Diseases, X-Linked, Middle Aged, Article, Anemia, Sideroblastic, Mitochondrial Proteins, Young Adult, Tyrosine-tRNA Ligase, MELAS Syndrome, Humans, Acidosis, Lactic, Female, Red Cell Biology & its Disorders, Genetic Association Studies, Germ-Line Mutation
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::6a45e11c567c6f28ad3a0a7859fd7703
https://pubmed.ncbi.nlm.nih.gov/30026338