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electricity (128) 128
science & technology (123) 123
basic electric elements (115) 115
processes or means, e.g. batteries, for the direct conversionof chemical into electrical energy (115) 115
life sciences & biomedicine (107) 107
humans (95) 95
male (74) 74
performing operations (66) 66
transporting (66) 66
vehicles in general (64) 64
female (60) 60
electric equipment or propulsion of electrically-propelledvehicles (59) 59
electrodynamic brake systems for vehicles, in general (59) 59
magnetic suspension or levitation for vehicles (59) 59
genetics & heredity (55) 55
adult (47) 47
physics (47) 47
measuring (43) 43
testing (43) 43
biological and medical sciences (41) 41
circuit arrangements or systems for supplying or distributingelectric power (41) 41
conversion or distribution of electric power (41) 41
generation (41) 41
systems for storing electric energy (41) 41
measuring electric variables (40) 40
measuring magnetic variables (40) 40
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virology (22) 22
medical genetics (21) 21
fundamental and applied biological sciences. psychology (20) 20
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chromosome deletion (17) 17
genotype (17) 17
microbiology (17) 17
biochemistry & molecular biology (16) 16
hiv-1 - genetics (15) 15
immunology (15) 15
analysis (14) 14
comparative genomic hybridization (14) 14
genes (14) 14
genetic aspects (14) 14
molecular sequence data (14) 14
viral diseases (14) 14
hiv infections - virology (13) 13
human viral diseases (13) 13
pedigree (13) 13
physical sciences (13) 13
aids/hiv (12) 12
cytogenetics (12) 12
medical education (12) 12
animals (11) 11
conjoint control of vehicle sub-units of different type ordifferent function (11) 11
control systems specially adapted for hybrid vehicles (11) 11
genotype & phenotype (11) 11
hiv infections - drug therapy (11) 11
human immunodeficiency virus--hiv (11) 11
research (11) 11
road vehicle drive control systems for purposes not related tothe control of a particular sub-unit (11) 11
abridged index medicus (10) 10
chemistry (10) 10
intellectual disability - genetics (10) 10
viral diseases of the lymphoid tissue and the blood. aids (10) 10
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abnormalities, multiple - genetics (9) 9
alleles (9) 9
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chromosome aberrations (9) 9
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physiological aspects (9) 9
sequence analysis, dna (9) 9
chemical sciences (8) 8
gene deletion (8) 8
general aspects. genetic counseling (8) 8
genetic association studies (8) 8
genetics of eukaryotes. biological and molecular evolution (8) 8
health aspects (8) 8
hiv envelope protein gp120 - genetics (8) 8
materials science (8) 8
research article (8) 8
virus diseases (8) 8
aged (7) 7
amino acid sequence (7) 7
antiretroviral therapy, highly active (7) 7
base sequence (7) 7
chromosome mapping (7) 7
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1. Full Text Zika virus: high infectious viral load in semen, a new sexually transmitted pathogen?
by Mansuy, Jean Michel and Dutertre, Marine and Mengelle, Catherine and Fourcade, Camille and Marchou, Bruno and Delobel, Pierre and Izopet, Jacques and Martin-Blondel, Guillaume
The Lancet infectious diseases, ISSN 1473-3099, 2016, Volume 16, Issue 4, pp. 405 - 405
Infectious Disease | Life Sciences & Biomedicine | Infectious Diseases | Science & Technology | Zika Virus - genetics | Humans | Zika Virus - physiology | RNA, Viral - analysis | Male | Zika Virus - isolation & purification | Viral Load | Sexually Transmitted Diseases, Viral - transmission | Zika Virus Infection - transmission | Zika Virus Infection - virology | Sexually Transmitted Diseases, Viral - virology | Adult | Semen - virology | Sexually transmitted diseases | Disease transmission | Urine | Antiretroviral drugs | Pathogens | Zika virus | Infections | Womens health | Index Medicus
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2. Full Text Holt-Oram syndrome: clinical and molecular description of 78 patients with TBX5 variants
by Vanlerberghe, Clémence and Jourdain, Anne-Sophie and Ghoumid, Jamal and Frenois, Frédéric and Mezel, Aurélie and Vaksmann, Guy and Lenne, Bruno and Delobel, Bruno and Porchet, Nicole and Cormier-Daire, Valérie and Smol, Thomas and Escande, Fabienne and Manouvrier-Hanu, Sylvie and Petit, Florence
European journal of human genetics : EJHG, ISSN 1018-4813, 2018, Volume 27, Issue 3, pp. 360 - 368
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Abnormalities, Multiple - pathology | Diagnosis, Differential | Humans | Heart Defects, Congenital - pathology | Infant | Upper Extremity Deformities, Congenital - pathology | Upper Extremity Deformities, Congenital - genetics | T-Box Domain Proteins - genetics | Heart Defects, Congenital - genetics | Phenotype | Heart Septal Defects, Atrial - genetics | Mutation | Lower Extremity Deformities, Congenital - genetics | Abnormalities, Multiple - genetics | Heart Septal Defects, Atrial - pathology | Lower Extremity Deformities, Congenital - pathology | Phenotypes | Diagnosis | Elbow | Genotypes | Defects | Holt-Oram syndrome | Index Medicus | Genetic counselling | Congenital heart defects | Disease genetics
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3. Full Text Zika virus in semen and spermatozoa
by Mansuy, Jean Michel and Suberbielle, Elsa and Chapuy-Regaud, Sabine and Mengelle, Catherine and Bujan, Louis and Marchou, Bruno and Delobel, Pierre and Gonzalez-Dunia, Daniel and Malnou, Cécile E and Izopet, Jacques and Martin-Blondel, Guillaume
The Lancet infectious diseases, ISSN 1473-3099, 2016, Volume 16, Issue 10, pp. 1106 - 1107
Infectious Disease | Life Sciences & Biomedicine | Infectious Diseases | Science & Technology | Urine | Antigens | Zika virus | Infections | Microscopy | Index Medicus | Life Sciences | Human health and pathology | Microbiology and Parasitology | Sexual reproduction | Emerging diseases | Reproductive Biology | Virology
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4. Full Text On the electrochemical impedance response of composite insertion electrodes – Toward a better understanding of porous electrodes
by Gruet, David and Delobel, Bruno and Sicsic, David and Lucas, Ivan T and Vivier, Vincent
Electrochimica acta, ISSN 0013-4686, 02/2019, Volume 295, pp. 787 - 800
Lithium-ion batteries | Porous electrode | Modeling | Single particle | Electrochemical impedance spectroscopy | Electrochemistry | Physical Sciences | Science & Technology | Electrodes | Electrolytes | Mathematical models | Porosity | Solid phases | Engineering Sciences | Electric power | Chemical Sciences
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5. Full Text Quantification of preferred orientation in graphite electrodes for Li-ion batteries with a novel X-ray-diffraction-based method
by Malifarge, Simon and Delobel, Bruno and Delacourt, Charles
Journal of power sources, ISSN 0378-7753, 03/2017, Volume 343, pp. 338 - 344
X-ray diffraction | Electrode | Anisotropy | Preferred orientation | Battery | Physical Sciences | Chemistry | Materials Science | Technology | Materials Science, Multidisciplinary | Electrochemistry | Chemistry, Physical | Energy & Fuels | Science & Technology | Electrodes | Batteries | Methods
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6. Full Text QTL mapping of the production of wine aroma compounds by yeast
by Steyer, Damien and Ambroset, Chloe and Brion, Christian and Claudel, Patricia and Delobel, Pierre and Sanchez, Isabelle and Erny, Claude and Blondin, Bruno and Karst, Francis and Legras, Jean-Luc
BMC genomics, ISSN 1471-2164, 10/2012, Volume 13, Issue 1, pp. 573 - 573
2-phenyl ethanol | ABZ1 | PLB2 | Rose oxide | Ethyl esters | QTL mapping | Citronellol | Nerolidol | QDR2 | Saccharomyces cerevisiae | Wine aroma | Farnesene | PDR8 | Genetics & Heredity | Life Sciences & Biomedicine | Biotechnology & Applied Microbiology | Science & Technology | Wine - microbiology | Sesquiterpenes - metabolism | Vitis - chemistry | Saccharomyces cerevisiae - genetics | Organic Chemicals - chemistry | Organic Chemicals - metabolism | Chromosome Mapping | Fermentation | Odorants | Genetic Variation | Saccharomyces cerevisiae - metabolism | Metabolic Networks and Pathways | Gene Deletion | Alleles | Monoterpenes - metabolism | Vitis - metabolism | Quantitative Trait Loci | Quantitative genetics | Wine | Quantitative trait loci | Metabolites | Grapes | Yeast fungi | Analysis | Genes | Physiological aspects | Esters | Instrument industry | Production data | Design | Yeast | Ethanol | Genomics | Principal components analysis | Genomes | Gene expression | Maximum likelihood method | Experiments | Index Medicus | Life Sciences
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7. Full Text The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients
by Leroy, Camille and Leroy, Camille and Landais, Emilie and Landais, Emilie and Briault, Sylvain and Briault, Sylvain and David, Albert and David, Albert and Tassy, Olivier and Tassy, Olivier and Gruchy, Nicolas and Gruchy, Nicolas and Delobel, Bruno and Delobel, Bruno and Grégoire, Marie-José and Grégoire, Marie-Jose and Leheup, Bruno and Leheup, Bruno and Taine, Laurence and Taine, Laurence and Lacombe, Didier and Lacombe, Didier and Delrue, Marie-Ange and Delrue, Marie-Ange and Toutain, Annick and Toutain, Annick and Paubel, Agathe and Paubel, Agathe and Mugneret, Francine and Mugneret, Francine and Thauvin-Robinet, Christel and Thauvin-Robinet, Christel and Arpin, Stéphanie and Arpin, Stephanie and Le Caignec, Cedric and Le Caignec, Cedric and Jonveaux, Philippe and Jonveaux, Philippe and Beri, Mylène and Beri, Mylene and Leporrier, Nathalie and Leporrier, Nathalie and Motte, Jacques and Motte, Jacques and Fiquet, Caroline and Fiquet, Caroline and Brichet, Olivier and Brichet, Olivier and Mozelle-Nivoix, Monique and Mozelle-Nivoix, Monique and Sabouraud, Pascal and Sabouraud, Pascal and Golovkine, Nathalie and Golovkine, Nathalie and Bednarek, Nathalie and Bednarek, Nathalie and Gaillard, Dominique and Gaillard, Dominique and Doco-Fenzy, Martine and Doco-Fenzy, Martine
European journal of human genetics : EJHG, ISSN 1018-4813, 06/2013, Volume 21, Issue 6, pp. 602 - 612
brachydactyly | AHO-like syndrome | overweight | 2q37-deletion syndrome | intellectual disability | genotype-phenotype correlation | Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Overweight - complications | Humans | Child, Preschool | Intellectual Disability - complications | Male | Intellectual Disability - genetics | Fibrous Dysplasia, Polyostotic - genetics | Young Adult | Chromosomes, Human, Pair 2 - genetics | Adult | Female | Behavior | Fibrous Dysplasia, Polyostotic - complications | Child | Chromosome Deletion | Genetic Association Studies | Chromosome Disorders - complications | Overweight - genetics | Chromosome Mapping | DNA Copy Number Variations - genetics | Comparative Genomic Hybridization | Brachydactyly - genetics | Adolescent | Brachydactyly - complications | Chromosome Disorders - genetics | Intellectual disabilities | Body weight | Hybridization | Gene deletion | French language | Literature reviews | Genotype & phenotype | Databases | Language | Clonal deletion | Cell cycle | Fluorescence in situ hybridization | Genetics | Period 2 protein | Brachydactyly | Genotypes | Seizures | Obesity | Phenotypes | Calpain | Gene expression | Chromosome 2 | Autism | Osteodystrophy | Collaboration | Index Medicus | Life Sciences | genotype–phenotype correlation
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8. Full Text 3D Quantification of Microstructural Properties of LiNi0.5Mn0.3Co0.2O2 High‐Energy Density Electrodes by X‐Ray Holographic Nano‐Tomography
by Nguyen, Tuan‐Tu and Villanova, Julie and Su, Zeliang and Tucoulou, Rémi and Fleutot, Benoît and Delobel, Bruno and Delacourt, Charles and Demortière, Arnaud
Advanced energy materials, ISSN 1614-6832, 02/2021, Volume 11, Issue 8, p. n/a
electrode microstructure | lithium‐ion batteries | nanoCT | microstructure analysis | X‐ray | Physical Sciences | Chemistry | Materials Science | Technology | Materials Science, Multidisciplinary | Physics, Condensed Matter | Chemistry, Physical | Energy & Fuels | Physics | Science & Technology | Physics, Applied | Attenuation coefficients | Electrodes | Flux density | Phase contrast | Morphology | Tomography | Attenuation | Microstructure | Design optimization | Quantitative analysis
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9. Full Text A recurrent tonsillitis
by Fourage, Marie, Dr and Bourguignat, Christophe, MD and Fermond, Bruno, MD and Delobel, Pierre, PhD
The Lancet (British edition), ISSN 0140-6736, 2013, Volume 381, Issue 9862, pp. 266 - 266
Internal Medicine | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Biological and medical sciences | General aspects | Medical sciences | Fusobacterium Infections - diagnosis | Recurrence | Tonsillitis - diagnosis | Humans | Adult | Fusobacterium necrophorum | Male | Tonsillitis - microbiology | Fusobacterium Infections - complications | Tonsillitis | Medical research | Bacteria | Infections | Bacterial infections | Index Medicus | Abridged Index Medicus
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10. Full Text High reactivity of the nickel-rich LiNi1-x-yMnxCoyO2 layered materials surface towards H2O/CO2 atmosphere and LiPF6-based electrolyte
by Martinez, Ana Cristina and Grugeon, Sylvie and Cailleu, Dominique and Courty, Matthieu and Tran-Van, Pierre and Delobel, Bruno and Laruelle, Stephane
Journal of power sources, ISSN 0378-7753, 08/2020, Volume 468, p. 228204
TG-MS | LiPO2F2 | Soluble base | Titration | NMC storage | Physical Sciences | Chemistry | Materials Science | Technology | Materials Science, Multidisciplinary | Electrochemistry | Chemistry, Physical | Energy & Fuels | Science & Technology | Inorganic chemistry | Chemical Sciences
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11. Full Text CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability
by Montagne, Louise and Derhourhi, Mehdi and Piton, Amélie and Toussaint, Bénédicte and Durand, Emmanuelle and Vaillant, Emmanuel and Thuillier, Dorothée and Gaget, Stefan and De Graeve, Franck and Rabearivelo, Iandry and Lansiaux, Amélie and Lenne, Bruno and Sukno, Sylvie and Desailloud, Rachel and Cnop, Miriam and Nicolescu, Ramona and Cohen, Lior and Zagury, Jean-François and Amouyal, Mélanie and Weill, Jacques and Muller, Jean and Sand, Olivier and Delobel, Bruno and Froguel, Philippe and Bonnefond, Amélie
Molecular metabolism (Germany), ISSN 2212-8778, 07/2018, Volume 13, pp. 1 - 9
Obesity | Augmented whole-exome sequencing | Copy number variation | Intellectual disability | Molecular diagnosis | Next-generation sequencing | Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Index Medicus
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12. Full Text A new mutational hotspot in the SKI gene in the context of MFS/TAA molecular diagnosis
by Arnaud, Pauline and Racine, Caroline and Hanna, Nadine and Thevenon, Julien and Alessandri, Jean-Luc and Bonneau, Dominique and Clayton-Smith, Jill and Coubes, Christine and Delobel, Bruno and Dupuis-Girod, Sophie and Gouya, Laurent and Odent, Sylvie and Carmignac, Virginie and Thauvin-Robinet, Christel and Le Goff, Carine and Jondeau, Guillaume and Boileau, Catherine and Faivre, Laurence
Human genetics, ISSN 0340-6717, 01/2020, Volume 139, Issue 4, pp. 461 - 472
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Proto-Oncogene Proteins - metabolism | Arachnodactyly - metabolism | Craniosynostoses - genetics | Humans | Middle Aged | Child, Preschool | Craniosynostoses - diagnosis | Male | Proto-Oncogene Proteins - genetics | DNA-Binding Proteins - genetics | Marfan Syndrome - genetics | Arachnodactyly - diagnosis | DNA-Binding Proteins - metabolism | Adolescent | Arachnodactyly - genetics | Marfan Syndrome - diagnosis | Marfan Syndrome - metabolism | Adult | Female | Mutation | Child | Pathology, Molecular | Craniosynostoses - metabolism | Learning disabilities | Genetic aspects | Diagnosis | Genes | Marfan syndrome | Marfan's syndrome | Phenotypes | Intellectual disabilities | Connective tissue diseases | Medical treatment | Surgery | Amino acids | Aorta | Thorax | Bone diseases | Index Medicus | Life Sciences
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