-
1دورية أكاديمية
المؤلفون: Yuhua Pan, Xiaoling Guo, Xiaoqiang Zhou, Yue Liu, Jingli Lian, Tingting Yang, Xiang Huang, Fei He, Jian Zhang, Buling Wu, Fu Xiong, Xingkun Yang
المصدر: Frontiers in Pediatrics, Vol 9 (2021)
مصطلحات موضوعية: global developmental delay (GDD), compound heterozygous missense mutations, corpus callosum anomaly, FRMD4A, intellectual disability, Pediatrics, RJ1-570
وصف الملف: electronic resource
-
2
المؤلفون: Lambert, J-C, Grenier-Boley, B., Harold, D., Zelenika, D., Chouraki, V., Kamatani, Y., Sleegers, K., Ikram, M. A., Hiltunen, M., Reitz, C., Mateo, I., Feulner, T., Bullido, M., Galimberti, D., Concari, L., Alvarez, V., Sims, R., Gerrish, A., Chapman, J., Deniz-Naranjo, C., Solfrizzi, V., Sorbi, S., Arosio, B., Spalletta, G., Siciliano, G., Epelbaum, J., Hannequin, D., Dartigues, J-F, Tzourio, C., Berr, C., Schrijvers, E. M. C., Rogers, R., Tosto, G., Pasquier, F., Bettens, K., Van Cauwenberghe, C., Fratiglioni, Laura, Graff, C., Delepine, M., Ferri, R., Reynolds, C. A., Lannfelt, L., Ingelsson, M., Prince, J. A., Chillotti, C., Pilotto, A., Seripa, D., Boland, A., Mancuso, M., Bossu, P., Annoni, G., Nacmias, B., Bosco, P., Panza, F., Sanchez-Garcia, F., Del Zompo, M., Coto, E., Owen, M., O'Donovan, M., Valdivieso, F., Caffara, P., Scarpini, E., Combarros, O., Buee, L., Campion, D., Soininen, H., Breteler, M., Riemenschneider, M., Van Broeckhoven, C., Alperovitch, A., Lathrop, M., Tregouet, D-A, Williams, J., Amouyel, P.
المصدر: Molecular Psychiatry. 18(4):461-470
وصف الملف: print
-
3
المؤلفون: Samuele Bovo, Silvia Tinarelli, Mohamad Ballan, Maurizio Gallo, Giuseppina Schiavo, Stefania Dall'Olio, Anisa Ribani, Luca Fontanesi, Valerio Joe Utzeri
المساهمون: Bovo S., Ballan M., Schiavo G., Ribani A., Tinarelli S., Utzeri V.J., Dall'Olio S., Gallo M., Fontanesi L.
المصدر: Animal Genetics
مصطلحات موضوعية: 0301 basic medicine, Genetic Markers, VRTN, Population, Sus scrofa, Genome Scan, Genome-wide association study, Single-nucleotide polymorphism, ARL4C, Biology, Quantitative trait locus, FRMD4A, Genome, 03 medical and health sciences, Mammary Glands, Animal, single nucleotide polymorphism, Genetic Marker, Genetics, Landrace, Animals, education, Genetic association, education.field_of_study, Full Paper, Animal, 0402 animal and dairy science, 04 agricultural and veterinary sciences, General Medicine, Full Papers, 040201 dairy & animal science, Genetic architecture, 030104 developmental biology, Haplotypes, Large White, Animal Science and Zoology, Female, morphological trait, HOXB1, Genome-Wide Association Study
وصف الملف: ELETTRONICO
-
4دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
5
المؤلفون: Rami Beiram, Sheikh Azimullah, Richard L. Jayaraj
المصدر: Saudi Journal of Biological Sciences, Vol 27, Iss 2, Pp 736-750 (2020)
Saudi Journal of Biological Sciencesمصطلحات موضوعية: GSK-3β, Glycogen synthase kinase 3 beta, 0106 biological sciences, 0301 basic medicine, MRI, Magnetic resonance imaging, ECE-1, Endotherin converting enzyme 1, IR, Insulin receptor, Type 2 diabetes, Disease, Bioinformatics, 01 natural sciences, LPA, Lipophosphatidic acid, Diabetes mellitus, BACE1, Beta-secretase 1, Arab population, ADAMTS9, ADAM Metallopeptidase With Thrombospondin Type 1 Motif 9, Medicine, Glucose homeostasis, lcsh:QH301-705.5, MC4R, Melanocortin 4 receptor, IGF-1, Insulin-like growth factor 1, NDUFS3, NADH:Ubiquinone Oxidoreductase Core Subunit S3, biology, NF-κB, nuclear factor kappa-light-chain-enhancer of activated B cells, RAB1A, Ras-related protein 1A, Insulin signaling, FRMD4A, FERM Domain Containing 4A, NFT, Neurofibrillary tangles, TFAP2B, Transcription Factor AP-2 Beta, BBB, Blood-Brain Barrier, Pit-PET, Pittsburgh compound B- positron emission tomography, FDG-PET, Fluorodeoxyglucose- positron emission tomography, Anti-diabetic drugs, T1DM, Type 1 Diabetes Mellitus, PP2A, Protein phosphatase 2, ApoE, Apolipoprotein E, General Agricultural and Biological Sciences, Alzheimer’s disease, IR, Insulin resistance, MCI, Myocardial infarction, TCF7L2, Transcription Factor 7 Like 2, PI3K, Phosphoinositide-3, NOTCH4, Neurogenic locus notch homolog protein 4, AGPAT1, 1-acyl-sn-glycerol-3-phosphate acyltransferase alpha, BMI, Body mass index, MENA, Middle East North African, AAV, Adeno-associated virus, AD, Alzheimer’s disease, Article, CALR, calreticulin gene, 03 medical and health sciences, Insulin resistance, FTO, Fat Mass and Obesity Associated Gene, GLP-1, Glucagon like peptide, Dementia, Aβ, Amyloid-beta, SORT, Sortilin, PPAR-γ2, Peroxisome proliferator-activated receptor gamma 2, CSF, Cerebrospinal fluid, MG-H1, Methylglyoxal-hydroimidazolone isomer trifluoroactic acid salt, COX-2, Cyclooxygenase 2, business.industry, DM, Diabetes mellitus, STZ, Streptozotocin, medicine.disease, CIP2A, Cancerous Inhibitor Of Protein Phosphatase 2A, Obesity, Insulin receptor, 030104 developmental biology, DUSP9, Dual Specificity Phosphatase 9, lcsh:Biology (General), ABCA1, ATP binding cassette subfamily A member 1, IDE, Insulin degrading enzyme, biology.protein, GNPDA2, Glucosamine-6-phosphate deaminase 2, business, T2DM, Type 2 Diabetes Mellitus, 010606 plant biology & botany
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82087843d8727a5c0d4d07ba5ff6b9bd
http://www.sciencedirect.com/science/article/pii/S1319562X19303286 -
6دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
7دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
8
المؤلفون: Jun Chen, Bo Jia, Jie Pan, Weitao Hu, Jianjiang Zhao, Hongxing Chu, Jiusong Han, Xiaoling Qiu, Xi Lin, Xianghuai Zheng, Xiang Sun
المصدر: International Journal of Molecular Medicine
مصطلحات موضوعية: Male, 0301 basic medicine, Pathology, medicine.medical_specialty, Blotting, Western, Cell, tongue squamous cell carcinoma, FRMD4A, Biology, Flow cytometry, Metastasis, gene silencing, 03 medical and health sciences, 0302 clinical medicine, Cell Movement, Tongue, Cell Line, Tumor, Genetics, medicine, Humans, Gene silencing, Neoplasm Invasiveness, Adaptor Proteins, Signal Transducing, Cell Proliferation, Retrospective Studies, medicine.diagnostic_test, Oncogene, Reverse Transcriptase Polymerase Chain Reaction, Cell Cycle, Cancer, Articles, General Medicine, Middle Aged, Cell cycle, medicine.disease, Immunohistochemistry, Tongue Neoplasms, Gene Expression Regulation, Neoplastic, 030104 developmental biology, medicine.anatomical_structure, 030220 oncology & carcinogenesis, CAL27, Carcinoma, Squamous Cell, Female, RNA Interference
-
9
المؤلفون: Mustafa A. Salih, Basma Abadel, Elliott H. Sherr, Stefan T. Arold, Mohammed Al-Owain, Amal Alhashem, Christopher A. Walsh, Fowzan S. Alkuraya, Jennifer N. Partlow, Ghada A. Otaify, Samira Sogati, Ali H Alwadei, Mohammed Zain Seidahmed, Saud Alsahli, Fahad A. Bashiri, Maha Tulbah, Nour Ewida, Samia A. Temtamy, Fahad Al-Hazzani, Brieana Fregeau, Eman Alobeid, Mona Aglan, Maha S. Zaki, Saeed Al Tala, Amal Y. Kentab, Muddathir H Hamad, Tarfa Al-Sheddi, Katta M. Girisha, Serdar Şahintürk, Niema Ibrahim, Zainab Al-Humaidi, Ghada M H Abdel-Salam, Salwa M. Alkhalifi, Mohamed Abouelhoda, Mais Hashem, Rana Alomar, Saad AlShahwan, Firdous Abdulwahab, Ranad Shaheen, Muna Al Saffar, Eissa Faqeih, Sateesh Maddirevula, Anas M. Alazami, Brahim Tabarki, Nisha Patel, Ameen Softah, Afaque Ahmad Imtiyaz Momin
المساهمون: Bursa Uludağ Üniversitesi/Tıp Fakültesi/Temel Tıp Bilimleri Anabilim Dalı., Şahintürk, Serdar
المصدر: Genetics in medicine : official journal of the American College of Medical Genetics
مصطلحات موضوعية: Cep135, 0301 basic medicine, Male, dwarfism, Yars gene, Intellectual disability, Dwarfism, Postnatal microcephaly, Procedures, Gene, Gene locus, Families, Cep135 gene, Genetic heterogeneity, Map1b gene, 0302 clinical medicine, Locus heterogeneity, Mechanisms, Truncating mutation, Autosomal Recessive Primary Microcephaly, Microcephaly, Ankle2 gene, Child, Genetics (clinical), Exome sequencing, Thg1L gene, Allele, Genetics, Transfer-rna, primary microcephaly, Genetics & heredity, Genomics, Pedigree, Nuclear magnetic resonance imaging, Phenotype, Child, Preschool, Recessive mutations, symbols, Female, medicine.symptom, Human, Adult, Genotype, Major clinical study, Biology, autozygome, Pathophysiology, Short stature, Article, 03 medical and health sciences, symbols.namesake, Frmd4a gene, Exome Sequencing, medicine, Humans, CNTRL, Ccnh gene, Preschool, Bptf gene, Disease severity, Form, Genetic regulation, Whole exome sequencing, Infant, Newborn, Infant, Genome analysis, Ppfibf1 gene, Newborn, medicine.disease, Human genetics, 030104 developmental biology, Preschool child, Mutation, Mendelian inheritance, Genetic variability, Primordial dwarfism, Controlled study, 030217 neurology & neurosurgery
وصف الملف: application/pdf
-
10
المؤلفون: P. Bosco, Rebecca Sims, Monique M.B. Breteler, L. Concari, Giuseppe Tosto, María J. Bullido, Kristel Sleegers, Fernando Valdivieso, Diana Zelenika, T. Feulner, Raffaele Ferri, Christophe Tzourio, P. Caffara, Davide Seripa, Benjamin Grenier-Boley, Paola Bossù, C. Chillotti, Marc Delepine, C. Deniz-Naranjo, Daniela Galimberti, David-Alexandre Trégouët, Benedetta Nacmias, Elisabeth M. C. Schrijvers, Karolien Bettens, Anne Boland, Christiane Reitz, Florentino Sanchez-Garcia, Dominique Campion, R. Rogers, C. Van Broeckhoven, Jean-Charles Lambert, Denise Harold, Amy Gerrish, Didier Hannequin, Mohammad Arfan Ikram, Michael Conlon O'Donovan, Elio Scarpini, Giorgio Annoni, Vincent Chouraki, Marc Lathrop, Francesco Panza, Chandra A. Reynolds, Gabriele Siciliano, Sandro Sorbi, Philippe Amouyel, Florence Pasquier, Luc Buée, Mikko Hiltunen, Claudine Berr, Eliecer Coto, Victoria Alvarez, Caroline Graff, Vincenzo Solfrizzi, Julie Williams, Jonathan A. Prince, Martin Ingelsson, Michael John Owen, Laura Fratiglioni, Jennifer Chapman, Ignacio Mateo, Annick Alpérovitch, H. Soininen, Michelangelo Mancuso, G. Spalletta, Matthias Riemenschneider, Andrea Pilotto, C. Van Cauwenberghe, Jacques Epelbaum, M. Del Zompo, Onofre Combarros, Lars Lannfelt, Yoichiro Kamatani, Beatrice Arosio, Jean-François Dartigues
المساهمون: Inserm U744, Epidémiologie des maladies chroniques : impact des interactions gène environnement sur la santé des populations, Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille, Droit et Santé-Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille, Droit et Santé, Cardiff University, Bioinformatics, GlaxoSmithKline, Centre National de Génotypage (CNG), Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Institut des Neurosciences de Montpellier (INM), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Centre d'Etude du Polymorphisme Humain (CEPH), Université Paris Diderot - Paris 7 (UPD7)-Institut Universitaire d'Hématologie (IUH), Université Paris Diderot - Paris 7 (UPD7)-Fondation Jean Dausset, Neurodegenerative Brain Diseases group, Department of Molecular Genetics, VIB, Antwerpen, Belgium, Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Antwerpen, Belgium, University of Antwerp (UA), Erasmus University Medical Center [Rotterdam] (Erasmus MC), University of Eastern Finland, G.H. Sergievsky Center, Columbia University, New York, NY, USA, Columbia University Irving Medical Center (CUIMC), Service of Neurology, University Hospital Marques de Valdecilla, University of Cantabria, Santander, Spain, Department of Psychiatry and Psychotherapy, Universitätsklinikum des Saarlandes, Universität des Saarlandes Saarbruecken, Germany, Centro de Biología Molecular Severo Ochoa [Madrid] (CBMSO), Universidad Autónoma de Madrid (UAM)-Consejo Superior de Investigaciones Científicas [Madrid] (CSIC), Centro Dino Ferrari [Milano], Università degli Studi di Milano = University of Milan (UNIMI)-Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, Department of Neuroscience, University of Parma, Parma, Italy, Università degli studi di Parma = University of Parma (UNIPR), Genética Molecular-Laboratorio de Medicina, Hospital Universitario Central Asturias, Oviedo, Spain, Servicio de Inmunología. Hospital Unviersitario de Gran Canaria Dr Negrín. Bco, Las Palmas de Gran Canaria, Spain, Department of Geriatrics, Center for aging brain, Memory unit, University of Bari, Bari, Italy, Università degli studi di Bari Aldo Moro = University of Bari Aldo Moro (UNIBA), Department of neurological and psychiatric Sciences, University of Florence, Florence, Italy, Università degli Studi di Firenze = University of Florence (UniFI), Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, Clinical and Behavioral Neurology, IRCCS Fondazione Santa Lucia, Roma, Italy, Clinical and Behavioral Neurology - Neuroscienze e riabilitazione, IRCCS Fondazione Santa Lucia [Roma], Neurological clinic, University of Pisa, Pisa, Italy, University of Pisa - Università di Pisa, Centre de Psychiatrie et Neurosciences (U894), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Génétique médicale et fonctionnelle du cancer et des maladies neuropsychiatriques, Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Génétique du cancer et des maladies neuropsychiatriques (GMFC), Epidémiologie et Biostatistique [Bordeaux], Université Bordeaux Segalen - Bordeaux 2-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), Neuroépidémiologie, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Neuropsychiatrie : recherche épidémiologique et clinique (PSNREC), Université Montpellier 1 (UM1)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Aging Research Center [Karolinska Institutet] (ARC ), Stockholm University-Karolinska Institutet [Stockholm], Department of Geriatric Medicine, Karolinska University Hospital, Stockholm, Sweden, KI-Alzheimer's Disease Reseach Center, Department NVS, Karolinska Institutet, KIADRC, Stockholm, Sweden, IRCCS Associazione Oasi Maria SS, Institute for Research on Mental Retardation and Brain Aging, Troina (EN), Italy, Department of Psychology [Riverside], University of California [Riverside] (UC Riverside), University of California (UC)-University of California (UC), Department of Public health and Caring Sciences, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden, Uppsala University, Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden, Unit of Clinical Pharmacology, Teaching Hospital of Cagliari, Cagliari, Italy, Geriatric Unit & Gerontology-Geriatrics Research Laboratory, Department of Medical Sciences, I.R.C.C.S. 'Casa Sollievo della Sofferenza', San Giovanni Rotondo, Italy, Università degli Studi di Cagliari = University of Cagliari (UniCa), Centre de Recherche Jean-Pierre AUBERT Neurosciences et Cancer - U837 (JPArc), Université Lille Nord de France (COMUE)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille, DZNE, Bonn, Germany, Génomique cardiovasculaire, Unité de Recherche sur les Maladies Cardiovasculaires, du Métabolisme et de la Nutrition = Research Unit on Cardiovascular and Metabolic Diseases (ICAN), Université Pierre et Marie Curie - Paris 6 (UPMC)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU), This work was supported by the National Foundation for Alzheimer's disease and related disorders, the Institut Pasteur de Lille, the Centre National de Génotypage, Inserm, FRC (fondation sur la recherche sur le cerveau) and Rotary., EADI consortium, GERAD consortium, Medical Research Council (MRC) Centre for Neuropsychiatric Genetics and Genomics, Neurosciences and Mental Health Research Institute, Department of Psychological Medicine and Neurology, School of Medicine, Cardiff University, Cardiff, UK, Institut des Neurosciences de Montpellier - Déficits sensoriels et moteurs (INM), Department of neurology, University of Eastern Finland and Kuopio University Hospital, Kuopio, Finland, Department of neurology, University of Eastern Finland-University Hospital of Kuopio-University of Eastern Finland-University Hospital of Kuopio, Universidad Autonoma de Madrid (UAM)-Consejo Superior de Investigaciones Científicas [Madrid] (CSIC), Università degli Studi di Milano [Milano] (UNIMI)-Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, Università degli studi di Bari Aldo Moro (UNIBA), Università degli Studi di Firenze = University of Florence [Firenze] (UNIFI), Institut de psychiatrie et neurosciences (U894 / UMS 1266), University of California [Riverside] (UCR), University of California-University of California, Section of Clinical Pharmacology, Department of Neurosciences 'B.B. Brodie', University of Cagliari, Cagliari, Italy, Centre de Recherche Jean-Pierre AUBERT Neurosciences et Cancer - U1172 Inserm - U837 (JPArc), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Lille Nord de France (COMUE)-Université de Lille, Unité de Recherche sur les Maladies Cardiovasculaires, du Métabolisme et de la Nutrition = Institute of cardiometabolism and nutrition (ICAN), Lambert, J, Grenier Boley, B, Harold, D, Zelenika, D, Chouraki, V, Kamatani, Y, Sleegers, K, Ikram, M, Hiltunen, M, Reitz, C, Mateo, I, Feulner, T, Bullido, M, Galimberti, D, Concari, L, Alvarez, V, Sims, R, Gerrish, A, Chapman, J, Deniz Naranjo, C, Solfrizzi, V, Sorbi, S, Arosio, B, Spalletta, G, Siciliano, G, Epelbaum, J, Hannequin, D, Dartigues, J, Tzourio, C, Berr, C, Schrijvers, E, Rogers, R, Tosto, G, Pasquier, F, Bettens, K, Van Cauwenberghe, C, Fratiglioni, L, Graff, C, Delepine, M, Ferri, R, Reynolds, C, Lannfelt, L, Ingelsson, M, Prince, J, Chillotti, C, Pilotto, A, Seripa, D, Boland, A, Mancuso, M, Bossù, P, Annoni, G, Nacmias, B, Bosco, P, Panza, F, Sanchez Garcia, F, Del Zompo, M, Coto, E, Owen, M, O'Donovan, M, Valdivieso, F, Caffara, P, Scarpini, E, Combarros, O, Buée, L, Campion, D, Soininen, H, Breteler, M, Riemenschneider, M, Van Broeckhoven, C, Alpérovitch, A, Lathrop, M, Trégouët, D, Williams, J, Amouyel, P, Epidemiology, Radiology & Nuclear Medicine, Neurology, Grenier-Boley, Benjamin, Réseau International des Instituts Pasteur ( RIIP ) -Réseau International des Instituts Pasteur ( RIIP ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Université de Lille, Droit et Santé-Institut Pasteur de Lille, Réseau International des Instituts Pasteur ( RIIP ) -Réseau International des Instituts Pasteur ( RIIP ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Université de Lille, Droit et Santé, Centre National de Génotypage ( CNG ), Commissariat à l'énergie atomique et aux énergies alternatives ( CEA ), Institut des Neurosciences de Montpellier - Déficits sensoriels et moteurs ( INM ), Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Université de Montpellier ( UM ), Centre d'Etude du Polymorphisme Humain ( CEPH ), Université Paris Diderot - Paris 7 ( UPD7 ) -Institut Universitaire d'Hématologie ( IUH ), Université Paris Diderot - Paris 7 ( UPD7 ) -Fondation Jean Dausset, Departement of Epidemiology and Radiology, Erasmus MC, Rotterdam, Centro de Biologia Molecular Severo Ochoa (UAM-CSIC) and CIBERNED, Universidad Autonoma, Madrid, Spain, Università degli studi di Milano [Milano]-Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, Department of Internal Medicine, Geriatric Unit, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Università degli Studi di Milano, Milan, Italy, University of Pisa [Pisa], Centre de Psychiatrie et Neurosciences ( CPN - U894 ), Université Paris Descartes - Paris 5 ( UPD5 ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ), Université de Rouen Normandie ( UNIROUEN ), Normandie Université ( NU ) -Normandie Université ( NU ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ), Génétique du cancer et des maladies neuropsychiatriques ( GMFC ), Université Bordeaux Segalen - Bordeaux 2-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale ( INSERM ), Université Pierre et Marie Curie - Paris 6 ( UPMC ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ), Neuropsychiatrie : recherche épidémiologique et clinique, Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Université Montpellier 1 ( UM1 ) -Université de Montpellier ( UM ), Department of Epidemiology and Neurology, Erasmus MC, Rotterdam, Centre Hospitalier Régional Universitaire [Lille] ( CHRU Lille ), Aging Reasearch Center, Department NVS, Karolinska Institutet and Stockholm University, Stockholm, Sweden, University of California [Riverside] ( UCR ), Centre de recherche Jean-Pierre Aubert-Neurosciences et Cancer, Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Université de Lille, Droit et Santé, Department of Epidemiology, Erasmus MC, Rotterdam, Unité de Recherche sur les Maladies Cardiovasculaires, du Métabolisme et de la Nutrition = Institute of cardiometabolism and nutrition ( ICAN ), Université Pierre et Marie Curie - Paris 6 ( UPMC ) -Assistance publique - Hôpitaux de Paris (AP-HP)-Institut National de la Santé et de la Recherche Médicale ( INSERM ) -CHU Pitié-Salpêtrière [APHP]
المصدر: Digital.CSIC. Repositorio Institucional del CSIC
instname
Molecular psychiatry
Europe PubMed Central
Molecular Psychiatry
Molecular Psychiatry, 2012, 18, pp.521-521. ⟨10.1038/mp.2012.75⟩
Molecular Psychiatry, Nature Publishing Group, 2012, 18, pp.521-521. ⟨10.1038/mp.2012.75⟩
Molecular Psychiatry, 18(4), 461-470. Nature Publishing Group
Molecular psychiatry 18(4), 461-470 (2012). doi:10.1038/mp.2012.14
Molecular Psychiatry, Nature Publishing Group, 2012, 18, pp.521-521. 〈10.1038/mp.2012.75〉مصطلحات موضوعية: Apolipoprotein E, haplotype, FERM domain-containing protein 4A, human, genetics [Alzheimer Disease], Genome-wide association study, Disease, Genome, Plasma, 0302 clinical medicine, genetics [Adaptor Proteins, Signal Transducing], blood [Amyloid beta-Peptides], GWAS, genetics [Genetic Predisposition to Disease], [ SDV.GEN.GH ] Life Sciences [q-bio]/Genetics/Human genetics, Genetics, 0303 health sciences, FRMD4A gene, amyloid, [ SDV.SPEE ] Life Sciences [q-bio]/Santé publique et épidémiologie, GWAS study, Alzheimer, FRMD4A, Alzheimer's disease, 3. Good health, Psychiatry and Mental health, Chemistry, genetics [Polymorphism, Single Nucleotide], Original Article, Corrigendum, medicine.medical_specialty, Amyloid, Single-nucleotide polymorphism, Locus (genetics), genome wide haplotype association study, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Cellular and Molecular Neuroscience, blood [Alzheimer Disease], Alzheimer Disease, genetics [Haplotypes], Genetic predisposition, medicine, Humans, Genetic Predisposition to Disease, ddc:610, Psychiatry, Molecular Biology, plasma, Genetic association, Adaptor Proteins, Signal Transducing, 030304 developmental biology, Amyloid beta-Peptides, business.industry, Haplotype, Case-control study, Haplotypes, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, [SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologie, Case-Control Studies, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, Human medicine, business, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: pdf; application/pdf
Full Text Finder 
Find this article in full text from Springer Verlag.