المؤلفون: Eva Gimeno, Margarita Ortega, Silvia Ramos-Campoy, Francesc Bosch, Tycho Baumann, Sandrine Bougeon, Florence Nguyen-Khac, Helen Parker, Carolina Moreno, Anna Puiggros, Blanca Espinet, Xavier Calvo, María José Calasanz, María José Larrayoz, David Oscier, Rosa Collado, Claudia Haferlach, María Laura Blanco, Jacqueline Schoumans, Rocío Salgado, Gian Matteo Rigolin, Sílvia Beà, Antonio Cuneo, Jonathan C. Strefford, Dolors Costa

المساهمون: Institut Català de la Salut, [Ramos-Campoy S, Puiggros A] Molecular Cytogenetics Laboratory, Pathology Department, Hospital del Mar, Barcelona, Spain. Translational Research on Hematological Neoplasms Group, Cancer Research Program, Institut Hospital del Mar d’Investigacions Mèdiques (IMIM), Barcelona, Spain. [Beà S, Costa D] Hematopathology Unit, Hospital Clínic, Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), CIBERONC, Barcelona, Spain. [Bougeon S] Oncogenomic Laboratory, Hematology Service, Lausanne University Hospital, Lausanne, Switzerland. [Larráyoz MJ] Cytogenetics and Hematological Genetics Services, Department of Genetics, University of Navarra, Pamplona, Spain. [Ortega M, Bosch F] Servei d’Hematologia, Vall d'Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: HAEMATOLOGICA
r-FIHGUV. Repositorio Institucional de Producción Científica de la Fundación de Investigación del Hospital General de Valencia
instname
Dadun. Depósito Académico Digital de la Universidad de Navarra
Scientia
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau

مصطلحات موضوعية: Oncology, medicine.medical_specialty, Chronic lymphocytic leukemia, Leucèmia limfocítica crònica - Aspectes genètics, Biology, Genetic Phenomena::Genetic Variation::Mutation::Chromosome Aberrations [PHENOMENA AND PROCESSES], Risk Assessment, NO, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Complex Karyotype, Other subheadings::Other subheadings::/genetics [Other subheadings], medicine, Humans, In patient, microarrays, Chromosome Aberrations, Natural Science Disciplines::Biological Science Disciplines::Biology::Computational Biology::Genomics [DISCIPLINES AND OCCUPATIONS], Chronic lymphocytic leukmia, genomic complexity, Genome complexity, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Karyotype, Genomics, Hematology, Prognosis, medicine.disease, Leukemia, Lymphocytic, Chronic, B-Cell, Chromosome Banding, Genòmica, Anomalies cromosòmiques, Neoplasms::Neoplasms by Histologic Type::Leukemia::Leukemia, Lymphoid::Leukemia, B-Cell::Leukemia, Lymphocytic, Chronic, B-Cell [DISEASES], Área de Biomedicina, 030220 oncology & carcinogenesis, disciplinas de las ciencias naturales::disciplinas de las ciencias biológicas::biología::biología computacional::genómica [DISCIPLINAS Y OCUPACIONES], Mutation, Risk stratification, Cohort, DNA microarray, fenómenos genéticos::variación genética::mutación::aberraciones cromosómicas [FENÓMENOS Y PROCESOS], neoplasias::neoplasias por tipo histológico::leucemia::leucemia linfoide::leucemia de células B::leucemia linfocítica crónica de células B [ENFERMEDADES], 030215 immunology

وصف الملف: application/pdf; text

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0246e8a7bd7915b1adde1b3996bc485eTest
https://doi.org/10.3324/haematol.2020.274456Test

المؤلفون: David Gonzalez, Alexander W. Wyatt, Joaquin Mateo, Michelle Shiller, Leonard G. Gomella, Albrecht Stenzinger, Ros Eeles, Anders Bjartell, Frédérique Penault-Llorca, Federico Rojo

المساهمون: Imagerie Moléculaire et Stratégies Théranostiques (IMoST), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Clermont Auvergne (UCA), Centre Jean Perrin [Clermont-Ferrand] (UNICANCER/CJP), UNICANCER, Institut Català de la Salut, [Gonzalez D] Patrick G Johnston Centre for Cancer Research, Queen’s University, Belfast, UK. [Mateo J] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Stenzinger A] Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany. [Rojo F] Department of Pathology, IIS-Hospital Universitario Fundación Jiménez Díaz-CIBERONC, Madrid, Spain. [Shiller M] Department of Pathology, Baylor University Medical Center, Dallas, TX, USA. [Wyatt AW] Vancouver Prostate Centre, Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada, Vall d'Hebron Barcelona Hospital Campus

المصدر: Journal of Pathology: Clinical Research
Journal of Pathology: Clinical Research, Wiley Open Access, In press, ⟨10.1002/cjp2.203⟩
Scientia
The Journal of Pathology: Clinical Research
Gonzalez, D, Mateo, J, Stenzinger, A, Rojo, F, Shiller, M, Wyatt, A W, Penault-Llorca, F, Gomella, L G, Eeles, R & Bjartell, A 2021, ' Practical considerations for optimising homologous recombination repair mutation testing in patients with metastatic prostate cancer ', The Journal of Pathology: Clinical Research . https://doi.org/10.1002/cjp2.203Test
The Journal of Pathology: Clinical Research, Vol 7, Iss 4, Pp 311-325 (2021)

مصطلحات موضوعية: Male, Oncology, ADN - Reparació, Indoles, [SDV]Life Sciences [q-bio], Review, Other subheadings::Other subheadings::/drug therapy [Other subheadings], Poly (ADP-Ribose) Polymerase Inhibitor, Piperazines, Prostate cancer, chemistry.chemical_compound, 0302 clinical medicine, Clinical pathway, Pathology, RB1-214, Pathology, Molecular, ComputingMilieux_MISCELLANEOUS, 0303 health sciences, Otros calificadores::Otros calificadores::/genética [Otros calificadores], mCRPC, 3. Good health, Prostatic Neoplasms, Castration-Resistant, 030220 oncology & carcinogenesis, medicine.medical_specialty, Otros calificadores::Otros calificadores::/farmacoterapia [Otros calificadores], Poly(ADP-ribose) Polymerase Inhibitors, metastatic prostate cancer, homologous recombination repair, Pathology and Forensic Medicine, Olaparib, molecular diagnostics, fenómenos químicos::fenómenos bioquímicos::reparación del ADN::reparación del ADN por recombinación [FENÓMENOS Y PROCESOS], 03 medical and health sciences, SDG 3 - Good Health and Well-being, Metàstasi, Internal medicine, Other subheadings::Other subheadings::/genetics [Other subheadings], medicine, Humans, Rucaparib, 030304 developmental biology, Chemical Phenomena::Biochemical Phenomena::DNA Repair::Recombinational DNA Repair [PHENOMENA AND PROCESSES], business.industry, Prostatic Neoplasms, Recombinational DNA Repair, Pròstata - Càncer - Tractament, medicine.disease, Molecular diagnostics, Neoplasms::Neoplasms by Site::Urogenital Neoplasms::Genital Neoplasms, Male::Prostatic Neoplasms::Prostatic Neoplasms, Castration-Resistant [DISEASES], chemistry, poly(ADP‐ribose) polymerase inhibitors, neoplasias::neoplasias por localización::neoplasias urogenitales::neoplasias de los genitales masculinos::neoplasias de la próstata::neoplasias prostáticas resistentes a la castración [ENFERMEDADES], Mutation, Phthalazines, Personalized medicine, business, Homologous recombination

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3ac0b84518f6ea72980fcece1d656c4Test
https://doi.org/10.1002/cjp2.203Test

المؤلفون: Judith Abarca-Zabalía, Pilar López-Cotarelo, Manuel Comabella, Yolanda Aladro, Teresa Agudo-Jiménez, Belen Pilo, Elena Urcelay, Adela González-Jiménez, Laura Espino-Paisán

المساهمون: Institut Català de la Salut, [López-Cotarelo P, González-Jiménez A] Laboratorio de Investigación en Genética y Bases Moleculares de Enfermedades Complejas, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Madrid, Spain. Red Española de Esclerosis Múltiple (REEM), Madrid, Spain. [Agudo-Jiménez T, Abarca-Zabalía J] Laboratorio de Investigación en Genética y Bases Moleculares de Enfermedades Complejas, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Madrid, Spain. [Aladro Y, Pilo B] Neurology Department, Hospital Universitario de Getafe, Madrid, Spain. [Comabella M] Servei de Neurologia-Neuroimmunologia, Centre d’Esclerosi Múltiple de Catalunya (CEMCAT), Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. Red Española de Esclerosis Múltiple (REEM), Madrid, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Scientia

مصطلحات موضوعية: Male, Esclerosi múltiple - Aspectes genètics, T-Lymphocytes, Gene Expression, Autoimmunity, Basal (phylogenetics), fenómenos genéticos::variación genética::polimorfismo genético::polimorfismo de nucleótido único [FENÓMENOS Y PROCESOS], B-Lymphocytes, Multidisciplinary, Genètica humana, medicine.diagnostic_test, Otros calificadores::Otros calificadores::/genética [Otros calificadores], CD69, Nervous System Diseases::Autoimmune Diseases of the Nervous System::Demyelinating Autoimmune Diseases, CNS::Multiple Sclerosis [DISEASES], Middle Aged, Genetic Phenomena::Genetic Variation [PHENOMENA AND PROCESSES], enfermedades del sistema nervioso::enfermedades autoinmunitarias del sistema nervioso::enfermedades autoinmunes desmielinizantes del SNC::esclerosis múltiple [ENFERMEDADES], Medicine, Female, Adult, medicine.medical_specialty, Multiple Sclerosis, Science, Biology, Peripheral blood mononuclear cell, Polymorphism, Single Nucleotide, Article, Immune system, Western blot, Downregulation and upregulation, Internal medicine, fenómenos genéticos::variación genética [FENÓMENOS Y PROCESOS], medicine, Other subheadings::Other subheadings::/genetics [Other subheadings], Immunogenetics, Humans, Allele, Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide [PHENOMENA AND PROCESSES], Multiple sclerosis, Polimorfisme genètic, Genetic Variation, Membrane Proteins, medicine.disease, Gene regulation in immune cells, Endocrinology, Genetic markers, Carrier Proteins, Neurological disorders

وصف الملف: application/pdf; image/jpeg

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f388d85995737210bb8c4ee2f6acde1Test
http://europepmc.org/articles/PMC8560952Test

المؤلفون: Lurdes Planas-Cerezales, Elena G. Arias-Salgado, Cristina Berastegui, Ana Montes-Worboys, Rafaela González-Montelongo, José. M. Lorenzo-Salazar, Vanesa Vicens-Zygmunt, Marta Garcia-Moyano, Jordi Dorca, Carlos Flores, Rosario Perona, Antonio Román, María Molina-Molina

المساهمون: Institut Català de la Salut, [Planas-Cerezales L, Montes-Worboys A] ILD Multidisciplinary Unit, Hospital Universitari Bellvitge, IDIBELL, Universitat de Barcelona, Hospitalet de Llobregat, Spain. [Arias-Salgado EG] Biomedical Research Institute CSIC/UAM, IdIPAZ, Madrid, Spain. Centro de Investigación Biomédica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain. [Berastegui C, Román A] Servei de Pneumologia, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d'Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. [González-Montelongo R, Lorenzo-Salazar JM] Genomics Division, Instituto Tecnológico y de Energías Renovables, Santa Cruz de Tenerife, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Frontiers in Medicine, Vol 8 (2021)
Dipòsit Digital de la UB
Universidad de Barcelona
Frontiers in Medicine
Scientia

مصطلحات موضوعية: 0301 basic medicine, Telomerase, Medicine (General), Respiratory Tract Diseases::Lung Diseases::Lung Diseases, Interstitial [DISEASES], medicine.medical_treatment, law.invention, 0302 clinical medicine, telomere shortening, law, telomere disorders, Pulmonary fibrosis, Medicine, genetics, Surgical Procedures, Operative::Surgical Procedures, Operative::Transplantation::Organ Transplantation::Lung Transplantation [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], Original Research, interstitial lung disease, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Interstitial lung disease, General Medicine, Intensive care unit, medicine.anatomical_structure, medicine.medical_specialty, 03 medical and health sciences, R5-920, Internal medicine, Transplantation of organs, tissues, etc, Other subheadings::Other subheadings::/genetics [Other subheadings], lung transplantation, Lung transplantation, Fibrosi pulmonar - Aspectes genètics, Lung, pulmonary fibrosis, business.industry, Extracorporeal circulation, diagnóstico::pronóstico::resultado del tratamiento [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], Pulmó, Diagnosis::Prognosis::Treatment Outcome [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], medicine.disease, Transplantation, Trasplantament d'òrgans, Pulmons - Trasplantació, 030104 developmental biology, Anomalies cromosòmiques, 030228 respiratory system, enfermedades respiratorias::enfermedades pulmonares::enfermedades pulmonares intersticiales [ENFERMEDADES], Chromosome abnormalities, Avaluació de resultats (Assistència sanitària), intervenciones quirúrgicas::intervenciones quirúrgicas::trasplante::trasplante de órganos::trasplante de pulmón [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], Lungs, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0aa4da58bf0be019cbc0238aee38019Test
https://www.frontiersin.org/articles/10.3389/fmed.2021.695919/fullTest

المؤلفون: Marzia Del Re, David T. Miyamoto, Kenneth J. Pienta, Alejandro Athie, Arnulf Stenzl, Adam G. Sowalsky, Alexander W. Wyatt, Paul C. Boutros, Irene Casanova-Salas, Edwin M. Posadas, Joaquin Mateo

المساهمون: Institut Català de la Salut, [Casanova-Salas I, Athie A, Mateo J] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Boutros PC] Departments of Human Genetics and Urology, Institute for Precision Health and Jonsson Comprehensive Cancer Center, University of California, Los Angeles, CA, USA. [Del Re M] Unit of Clinical Pharmacology and Pharmacogenetics, Department of Clinical and Experimental Medicine, University Hospital of Pisa, Pisa, Italy. [Miyamoto DT] Department of Radiation Oncology, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA. [Pienta KJ] The James Buchanan Brady Urological Institute and Department of Urology, Johns Hopkins University School of Medicine, Baltimore, MD, USA, Vall d'Hebron Barcelona Hospital Campus

المصدر: European urology, vol 79, iss 6
Scientia

مصطلحات موضوعية: Oncology, Male, diagnóstico::toma de decisiones clínicas [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], 030232 urology & nephrology, Neoplastic Cells, Circulating Tumor DNA, Transcriptome, Prostate cancer, 0302 clinical medicine, Circulating tumor cell, Diagnosis::Diagnostic Techniques and Procedures::Clinical Laboratory Techniques::Cytological Techniques::Cytodiagnosis::Biopsy::Liquid Biopsy [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], Circulating, Cancer, screening and diagnosis, Tumor, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Precision medicine, Genomics, Extracellular vesicles, Urology & Nephrology, Neoplastic Cells, Circulating, diagnóstico::técnicas y procedimientos diagnósticos::técnicas de laboratorio clínico::técnicas citológicas::citodiagnóstico::biopsia::biopsia líquida [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], Detection, 030220 oncology & carcinogenesis, Diagnosis::Clinical Decision-Making [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], Pròstata - Càncer - Aspectes genètics, Biòpsia, Pròstata - Càncer - Presa de decisions, Biotechnology, 4.2 Evaluation of markers and technologies, Urologic Diseases, medicine.medical_specialty, Neoplasms::Neoplasms by Site::Urogenital Neoplasms::Genital Neoplasms, Male::Prostatic Neoplasms [DISEASES], Urology, Clinical Decision-Making, Clinical Sciences, Context (language use), 03 medical and health sciences, Clinical Research, Internal medicine, Biomarkers, Tumor, Other subheadings::Other subheadings::/genetics [Other subheadings], medicine, Genetics, Humans, Liquid biopsy, Circulating tumor DNA, business.industry, Human Genome, Prostatic Neoplasms, Epigenome, medicine.disease, 4.1 Discovery and preclinical testing of markers and technologies, neoplasias::neoplasias por localización::neoplasias urogenitales::neoplasias de los genitales masculinos::neoplasias de la próstata [ENFERMEDADES], Good Health and Well Being, Liquid Biopsy, Tumor progression, business, Biomarkers

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44876dd37defa804cb9ab8692907b642Test
https://escholarship.org/uc/item/8h9111fjTest

المؤلفون: Rita Beier, Marina Cavazzana, Figen Dogu, Yves Bertrand, Paul Veys, Francesca Ferrua, Robbert G. M. Bredius, Roland Meisel, Arnalda Lanfranchi, Renata Formankova, Stéphane Blanche, Virginie Courteille, Elena Soncini, Tayfun Güngör, Jolanta Gozdzik, Kim Vettenranta, Krzysztof Kałwak, Mikael Alligon, Natacha Entz-Werle, Ansgar Schulz, Nizar Mahlaoui, Savaş Kansoy, Wilhelm Friedrich, Amos Toren, Mehmet A. Yeşilipek, Alina Ferster, Andrew R. Gennery, Mary Slatter, Despina Moshous, Fulvio Porta, Marco Zecca, Anders Fasth, Karoline Ehlert, Gérard Michel, Bénédicte Neven, Victoria Bordon, Alphan Kupesiz, Mikael Sundin, Kanchan Rao, Cristina Diaz-de-Heredia, Isabelle Badell Serra, Michael H. Albert, Herbert Pichler, Arjan C. Lankester, Andrew J. Cant, Marta González-Vicent, Petr Sedlacek, Jose Moraleda, Caroline A. Lindemans, Peter Bader, Manfred Hoenig, Alain Fischer, Austen Worth, Dmitry Balashov, Erik G J von Asmuth, Carsten Speckmann, Nuno Miranda, Aydan Ikinciogullari

المساهمون: Clinicum, Children's Hospital, Lastentautien yksikkö, HUS Children and Adolescents, University of Zurich, Lankester, Arjan C, Institut Català de la Salut, [Lankester AC, von Asmuth EGJ] Pediatric Stem Cell Transplantation Program and Laboratory for Pediatric Immunology, Willem-Alexander Children’s Hospital, Leiden University Medical Center, Leiden, The Netherlands. [Neven B] Unité d’Immuno-hematologie et Rhumatologie Pédiatrique, Hôpital Universitaire Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France. Université de Paris, Paris, France. Institut Imagine, INSERM UMR1163, Laboratory of Immunogenetics of Pediatric Autoimmune Diseases, Paris, France. [Mahlaoui N, Courteille V, Alligon M] French National Reference Center for Primary Immunodeficiencies (CEREDIH) and European Registry for Stem Cell Transplantation for Primary Immunodeficiencies (SCETIDE), Hôpital Universitaire Necker-Enfants malades, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France. [Diaz-de-Heredia C] Servei d’Oncologia i Hematologia Pediàtriques, Vall d’Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Instituto de Salud Carlos III (ISCIII)
Journal of Allergy and Clinical Immunology, 149(5), 1744-1754.e8. MOSBY-ELSEVIER
Scientia

مصطلحات موضوعية: Oncology, Transplantation Conditioning, medicine.medical_treatment, Hematopoietic stem cell transplantation, Cohort Studies, 0302 clinical medicine, conditioning, Immunology and Allergy, OUTCOMES, 0303 health sciences, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Hematopoietic Stem Cell Transplantation, immune reconstitution, 3. Good health, surgical procedures, operative, medicine.anatomical_structure, Cohort, 2723 Immunology and Allergy, SURVIVAL, Malalties congènites, Unrelated Donors, medicine.medical_specialty, Immunology, 610 Medicine & health, pretransplantation infections, SCID, 03 medical and health sciences, Internal medicine, enfermedades y anomalías neonatales congénitas y hereditarias::enfermedades del recién nacido::inmunodeficiencia combinada grave [ENFERMEDADES], Other subheadings::Other subheadings::/genetics [Other subheadings], medicine, Humans, genetic subgroups, Interleukin-7 receptor, 030304 developmental biology, Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Infant, Newborn, Diseases::Severe Combined Immunodeficiency [DISEASES], 2403 Immunology, Severe combined immunodeficiency, Cèl·lules mare hematopoètiques - Trasplantació, business.industry, medicine.disease, Anti-thymocyte globulin, Transplantation, RECONSTITUTION, Graft-versus-host disease, 10036 Medical Clinic, 3121 General medicine, internal medicine and other clinical medicine, Severe Combined Immunodeficiency, Bone marrow, business, 030215 immunology

وصف الملف: PIIS0091674921016298.pdf - application/pdf; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3a166208b4a369dac2c837c1851bc17Test
https://doi.org/10.1016/j.jaci.2021.10.017Test

المؤلفون: Remuzgo-Martínez, Sara, Genre, Fernanda, Pulito-Cueto, Verónica, Atienza-Mateo, Belén, Mora Cuesta, Víctor Manuel, Iturbe Fernández, David, Fernández Rozas, Sonia María, Lera-Gómez, Leticia, Alonso Lecue, Pilar, Ussetti, María Piedad, Laporta, Rosalía, Berastegui García, Cristina, Solé, Amparo, Pérez González, Virginia Luz, De Pablo Gafas, Alicia, Gualillo, Oreste, Cifrián, José Manuel, López-Mejías, Raquel, Gonzalez-Gay, MA, Universitat Autònoma de Barcelona

المساهمون: Institut Català de la Salut, Vall d'Hebron Barcelona Hospital Campus, Universidad de Cantabria

المصدر: Biomedicines, Vol 9, Iss 458, p 458 (2021)
Biomedicines
Volume 9
Issue 5
Scientia
Biomedicines . 2021 Apr 22;9(5):458
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona

مصطلحات موضوعية: idiopathic interstitial pneumonia, medicine.medical_specialty, Pulmons - Malalties - Aspectes genètics, Respiratory Tract Diseases::Lung Diseases::Lung Diseases, Interstitial [DISEASES], QH301-705.5, Medicine (miscellaneous), Interstitial lung disease, Gastroenterology, General Biochemistry, Genetics and Molecular Biology, Pulmonary function testing, Enzymes and Coenzymes::Enzymes::Transferases::Phosphotransferases::Phosphotransferases (Alcohol Group Acceptor)::Protein Kinases::Protein-Tyrosine Kinases::Receptor Protein-Tyrosine Kinases::Receptors, Vascular Endothelial Growth Factor [CHEMICALS AND DRUGS], Lung Disorder, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Internal medicine, Genotype, Proteïnes quinases - Receptors, medicine, Other subheadings::Other subheadings::/genetics [Other subheadings], Genetics, genetics, Idiopathic interstitial pneumonia, Biology (General), health care economics and organizations, interstitial lung disease, vascular endothelial growth factor, business.industry, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Haplotype, Biomarker, respiratory system, medicine.disease, respiratory tract diseases, Vascular endothelial growth factor, 030228 respiratory system, chemistry, enfermedades respiratorias::enfermedades pulmonares::enfermedades pulmonares intersticiales [ENFERMEDADES], 030220 oncology & carcinogenesis, Biomarker (medicine), enzimas y coenzimas::enzimas::transferasas::fosfotransferasas::fosfotransferasas (grupo alcohol aceptor)::proteína cinasas::proteína-tirosina cinasas::receptores proteína-tirosina cinasas::receptores del factor de crecimiento del endotelio vascular [COMPUESTOS QUÍMICOS Y DROGAS], biomarker, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9b03977d86c2562597f540c38ff3003Test
https://www.mdpi.com/2227-9059/9/5/458Test

المؤلفون: Maria Rosario Chica Parrado, Maria Auxiliadora Gómez-España, Eduardo Díaz-Rubio, Manuel Benavides, Ana Vivancos, Marta Toledano, Enrique Aranda, Vanesa García-Barberán, Martina Alvarez, Elena Elez

المساهمون: Institut Català de la Salut, [Vivancos A] Grup de genòmica del Càncer, Vall d'Hebron Institut d'Oncologia, Barcelona, Spain. [Aranda E, Gómez-España MA] Department of Medical Oncology, Reina Sofía University Hospital, CIBERONC, Córdoba, Spain. [Benavides M] Department of Medical Oncology, Hospital Universitario Regional y Virgen de la Victoria, Málaga, Spain. [Élez E] Servei d’Oncologia Mèdica, Vall d'Hebron Institut d'Oncologia, Barcelona, Spain. [Toledano M] IMIBIC Instituto Maimonides Investigación Biomédica de Córdoba, Córdoba, Spain., Hospital Verge de la Cinta de Tortosa

المصدر: Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019)
Scientia
Recercat. Dipósit de la Recerca de Catalunya
instname
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Scientific Reports

مصطلحات موضوعية: 0301 basic medicine, Male, Colorectal cancer, Mutant, DNA Mutational Analysis, lcsh:Medicine, medicine.disease_cause, Gastroenterology, 0302 clinical medicine, Diagnosis::Diagnostic Techniques and Procedures::Clinical Laboratory Techniques::Cytological Techniques::Cytodiagnosis::Biopsy::Liquid Biopsy [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], Other subheadings::/diagnosis [Other subheadings], lcsh:Science, Early Detection of Cancer, enzimas y coenzimas::enzimas::hidrolasas::ácido anhídrido hidrolasas::GTP fosfohidrolasas::proteínas de unión al GTP::proteínas de unión al GTP monoméricas::proteínas ras::proteínas protooncogénicas p21(ras) [COMPUESTOS QUÍMICOS Y DROGAS], Aged, 80 and over, Mutation, Multidisciplinary, Otros calificadores::Otros calificadores::/genética [Otros calificadores], neoplasias::neoplasias por localización::neoplasias del sistema digestivo::neoplasias gastrointestinales::neoplasias intestinales::neoplasias colorrectales [ENFERMEDADES], Enzimas y Coenzimas::Enzimas::Hidrolasas::Ácido Anhídrido Hidrolasas::GTP Fosfohidrolasas::Proteínas de Unión al GTP::Proteínas de Unión al GTP Monoméricas::Proteínas ras::Proteínas Proto-Oncogénicas p21(ras) [COMPUESTOS QUÍMICOS Y DROGAS], Middle Aged, Prognosis, diagnóstico::técnicas y procedimientos diagnósticos::técnicas de laboratorio clínico::técnicas citológicas::citodiagnóstico::biopsia::biopsia líquida [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], Female, KRAS, Colorectal Neoplasms, Biòpsia, Cell-Free Nucleic Acids, Oncogens Ras, Neoplasias::Neoplasias por Localización::Neoplasias del Sistema Digestivo::Neoplasias Gastrointestinales::Neoplasias Intestinales::Neoplasias Colorrectales [ENFERMEDADES], Adult, medicine.medical_specialty, Concordance, Otros calificadores::/diagnóstico [Otros calificadores], Article, Cancer screening, Proto-Oncogene Proteins p21(ras), 03 medical and health sciences, Gastrointestinal cancer, Neoplasms::Neoplasms by Site::Digestive System Neoplasms::Gastrointestinal Neoplasms::Intestinal Neoplasms::Colorectal Neoplasms [DISEASES], Internal medicine, medicine, Biomarkers, Tumor, Other subheadings::Other subheadings::/genetics [Other subheadings], Humans, Liquid biopsy, Allele, neoplasms, Aged, Enzymes and Coenzymes::Enzymes::Hydrolases::Acid Anhydride Hydrolases::GTP Phosphohydrolases::GTP-Binding Proteins::Monomeric GTP-Binding Proteins::ras Proteins::Proto-Oncogene Proteins p21(ras) [CHEMICALS AND DRUGS], business.industry, lcsh:R, Liquid Biopsy, medicine.disease, digestive system diseases, 030104 developmental biology, Còlon - Càncer - Diagnòstic, lcsh:Q, business, 030217 neurology & neurosurgery, Kras mutation

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97c48f78c860ebc9726fe6397f0efd05Test
http://link.springer.com/article/10.1038/s41598-019-45616-yTest

المؤلفون: Nicholas van Buuren, Ricardo Ramirez, Cameron Soulette, Vithika Suri, Dong Han, Lindsey May, Scott Turner, P.C. Parvangada, Ross Martin, Henry L.Y. Chan, Patrick Marcellin, Maria Buti, Nam Bui, Neeru Bhardwaj, Anuj Gaggar, Li Li, Hongmei Mo, Becket Feierbach

المساهمون: Institut Català de la Salut, [van Buuren N, Ramirez R, Soulette C, Suri V, Han D, May L] Gilead Sciences Inc., Foster City, CA, USA. [Buti M] Vall d’Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Scientia

مصطلحات موضوعية: Transcripció genètica, Infections::Infections::Virus Diseases::DNA Virus Infections::Hepadnaviridae Infections::Hepatitis B::Infections::Virus Diseases::Hepatitis B, Chronic [DISEASES], Hepatology, Otros calificadores::Otros calificadores::/genetica [Otros calificadores], fenómenos químicos::fenómenos bioquímicos::transcripción genética [FENÓMENOS Y PROCESOS], Other subheadings::Other subheadings::/genetics [Other subheadings], Gastroenterology, Internal Medicine, Genetic Phenomena::Gene Expression::Transcription, Genetic [PHENOMENA AND PROCESSES], Immunology and Allergy, Hepatitis B - Aspectes genètics, virosis::infecciones por virus ADN::infecciones por Hepadnaviridae::hepatitis B::hepatitis B crónica [ENFERMEDADES]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d27e71d336449edfc1fcdeff7a95276fTest
https://doi.org/10.1016/j.jhepr.2022.100449Test

المؤلفون: Espen Saxhaug Kristoffersen, Ko Willems van Dijk, Aster V.E. Harder, Rigmor H. Jensen, Patricia Pozo-Rosich, Lisanne S. Vijfhuizen, Michel D. Ferrari, John-Anker Zwart, Laurent F. Thomas, Thomas F. Hansen, Emer O'Connor, G.M. Terwindt, Raymond Noordam, Frits R. Rosendaal, Lisette J. A. Kogelman, Rolf Fronczek, Erling Tronvik, Sigrid Børte, Arn M. J. M. van den Maagdenberg, Irene de Boer, Bendik S. Winsvold, Carmen Fourier

المساهمون: Institut Català de la Salut, [Harder AVE] Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands. Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands. [Winsvold BS] Department of Research, Innovation and Education, Division of Clinical Neuroscience, Oslo University Hospital, Oslo, Norway. K.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway. Department of Neurology, Oslo University Hospital, Oslo, Norway. [Noordam R] Department of Internal Medicine, Section of Gerontology and Geriatrics, Leiden University Medical Center, Leiden, The Netherlands. [Vijfhuizen LS] Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands. [Børte S] Department of Research, Innovation and Education, Division of Clinical Neuroscience, Oslo University Hospital, Oslo, Norway. K.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway. Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway. [Kogelman LJA] Department of Neurology, Danish Headache Center, Rigshospitalet, Glostrup, Denmark. [Pozo-Rosich P] Grup de Recerca en Cefalea, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. Unitat de Cefalea, Servei de Neurologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus, Complex Disease Genetics, Institute for Molecular Medicine Finland, Genomics of Neurological and Neuropsychiatric Disorders, University of Helsinki

المصدر: Annals of Neurology, 90(2), 203-216. WILEY
Scientia
Annals of Neurology
Harder, A V E, Winsvold, B S, Noordam, R, Vijfhuizen, L S, Børte, S, Kogelman, L J A, Boer, I, Tronvik, E, Rosendaal, F R, Willems Van Dijk, K, O'connor, E, Fourier, C, Thomas, L F, Kristoffersen, E S, Fronczek, R, Pozo-rosich, P, Jensen, R H, Ferrari, M D, Hansen, T F, Zwart, J, Terwindt, G M & Maagdenberg, A M J M 2021, ' Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache ', Annals of Neurology, vol. 90, no. 2, pp. 203-216 . https://doi.org/10.1002/ana.26146Test
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona

مصطلحات موضوعية: medicine.medical_specialty, Linkage disequilibrium, Genetic Phenomena::Genotype::Genetic Predisposition to Disease [PHENOMENA AND PROCESSES], Diàtesi, Single-nucleotide polymorphism, Genome-wide association study, 3124 Neurology and psychiatry, afecciones patológicas, signos y síntomas::procesos patológicos::atributos de la enfermedad::susceptibilidad a enfermedades::predisposición genética a la enfermedad [ENFERMEDADES], Internal medicine, medicine, Genetic predisposition, Other subheadings::Other subheadings::/genetics [Other subheadings], enfermedades del sistema nervioso::enfermedades del sistema nervioso central::enfermedades cerebrales::trastornos con cefaleas::cefaleas primarias::cefalalgia autónoma del trigémino::cefalea histamínica [ENFERMEDADES], Research Articles, business.industry, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Cluster headache, 3112 Neurosciences, Cefalàlgia - Aspectes genètics, Odds ratio, medicine.disease, Confidence interval, 3. Good health, Neurology, Nervous System Diseases::Central Nervous System Diseases::Brain Diseases::Headache Disorders::Headache Disorders, Primary::Trigeminal Autonomic Cephalalgias::Cluster Headache [DISEASES], Population study, Neurology (clinical), business, Research Article

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dcff5fa4403ed4b892b048f6c58b55cTest
https://ddd.uab.cat/record/256417Test