Search Results - "Abidi, E."

Wintertime aerosol chemical composition and source apportionment of the organic fraction in the metropolitan area of Paris by Crippa, M, DeCarlo, P. F, Slowik, J. G, Mohr, C, Heringa, M. F, Chirico, R, Poulain, L, Freutel, F, Sciare, J, Cozic, J, Di Marco, C. F, Elsasser, M, Nicolas, J. B, Marchand, N, Abidi, E, Wiedensohler, A, Drewnick, F, Schneider, J, Borrmann, S, Nemitz, E, Zimmermann, R, Jaffrezo, J.-L, Prévôt, A. S. H, Baltensperger, U

“…The effect of a post-industrial megacity on local and regional air quality was assessed via a month-long field measurement campaign in the Paris metropolitan…”
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Inter-comparison of source apportionment models for the estimation of wood burning aerosols during wintertime in an Alpine city (Grenoble, France) by Favez, O., El Haddad, I., Piot, C., Boréave, A., Abidi, E., Marchand, N., Jaffrezo, J.-L., Besombes, J.-L., Personnaz, M.-B., Sciare, J., Wortham, H., George, C., D'Anna, B.

“…The emission of organic aerosols (OA) in the ambient air by residential wood burning is nowadays a subject of great scientific concern and a growing number of…”
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Evolution of the physical parameters of photovoltaic generators as a function of temperature and irradiance: New method of prediction based on the manufacturer’s datasheet by Yadir, S., Bendaoud, R., EL-Abidi, A., Amiry, H., Benhmida, M., Bounouar, S., Zohal, B., Bousseta, H., Zrhaiba, A., Elhassnaoui, A.

“…[Display omitted] •New physical parameters extracting method based on PV module datasheet.•New physical parameters extracting method based on accurate (I, V)…”
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Primary and secondary organic aerosol origin by combined gas-particle phase source apportionment by Crippa, M, Canonaco, F, Slowik, J. G, El Haddad, I, DeCarlo, P. F, Mohr, C, Heringa, M. F, Chirico, R, Marchand, N, Temime-Roussel, B, Abidi, E, Poulain, L, Wiedensohler, A, Baltensperger, U, Prévôt, A. S. H

“…Secondary organic aerosol (SOA), a prominent fraction of particulate organic mass (OA), remains poorly constrained. Its formation involves several unknown…”
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Terahertz Detection by Asymmetric Dual Grating Gate Bilayer Graphene FETs with Integrated Bowtie Antenna by Abidi, E, Khan, A, Delgado-Notario, J A, Clericó, V, Calvo-Gallego, J, Taniguchi, T, Watanabe, K, Otsuji, T, Velázquez, J E, Meziani, Y M

“…An asymmetric dual-grating gate bilayer graphene-based field effect transistor (ADGG-GFET) with an integrated bowtie antenna was fabricated and its response as…”
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Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia by Abidi, F E, Holloway, L, Moore, C A, Weaver, D D, Simensen, R J, Stevenson, R E, Rogers, R C, Schwartz, C E

“…Mutations in the JARID1C (Jumonji AT-rich interactive domain 1C) gene were recently associated with X-linked mental retardation (XLMR). Mutations in this gene…”
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A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palate by Abidi, FE, Miano, MG, Murray, JC, Schwartz, CE

“…Recently, two truncating mutations in the PHF8 (plant homeodomain finger protein 8) gene have been found to cause X‐linked mental retardation associated with…”
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ARHGEF9 disruption in a female patient is associated with X linked mental retardation and sensory hyperarousal by Marco, E J, Abidi, F E, Bristow, J, Dean, W B, Cotter, P, Jeremy, R J, Schwartz, C E, Sherr, E H

“…We identified a female patient with mental retardation and sensory hyperarousal. She has a de novo paracentric inversion of one X chromosome with completely…”
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Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C by Grafodatskaya, Daria, Chung, Barian H Y, Butcher, Darci T, Turinsky, Andrei L, Goodman, Sarah J, Choufani, Sana, Chen, Yi-An, Lou, Youliang, Zhao, Chunhua, Rajendram, Rageen, Abidi, Fatima E, Skinner, Cindy, Stavropoulos, James, Bondy, Carolyn A, Hamilton, Jill, Wodak, Shoshana, Scherer, Stephen W, Schwartz, Charles E, Weksberg, Rosanna

“…A number of neurodevelopmental syndromes are caused by mutations in genes encoding proteins that normally function in epigenetic regulation. Identification of…”
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A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor by Ramser, Juliane, Abidi, Fatima E., Burckle, Celine A., Lenski, Claus, Toriello, Helga, Wen, Gaiping, Lubs, Herbert A., Engert, Stefanie, Stevenson, Roger E., Meindl, Alfons, Schwartz, Charles E., Nguyen, Genevieve

“…The renin–angiotensin system (RAS) is essential for blood pressure control and water–electrolyte balance. Until the discovery of the renin receptor, renin was…”
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Mutation in the 5' alternatively spliced region of the XNP/ATR-X gene causes Chudley-Lowry syndrome by Abidi, Fatima E, Cardoso, Carlos, Lossi, Anne-Marie, Lowry, Robert Brian, Depetris, Danielle, Mattéi, Marie-Geneviève, Lubs, Herbert A, Stevenson, Roger E, Fontes, Michel, Chudley, Albert E, Schwartz, Charles E

“…The Chudley-Lowry syndrome (ChLS, MIM 309490) is an X-linked recessive condition characterized by moderate to severe mental retardation, short stature, mild…”
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A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation by Teague, Jon, Van Esch, Hilde, Carvill, Gemma, Richardson, David, Varian, Jennifer, Wooster, Richard, Stratton, Michael R, O'Meara, Sarah, Hardy, Claire, Shepherd, Rebecca, Bobrow, Martin, Gardner, Alison, Abidi, Fatima E, Srivastava, Anand K, Fullston, Tod, Cole, Jennifer, Jenkinson, Andrew, Buck, Gemma, Tarpey, Patrick S, Futreal, P Andrew, Latimer, Calli, Turrell, Kelly, Jia, Mingming, Corbett, Mark, Boyle, Jackie, Luo, Ying, Partington, Michael, Gecz, Jozef, van Bokhoven, Hans, Andrews, Jenny, Blow, Matt, de Brouwer, Arjan P M, Cox, James, Whibley, Annabel, Rujirabanjerd, Sinitdhorn, Moon, Jenny, Mallya, Uma, Gray, Kristian, Dunmore, Rebecca, Smith, Raffaella, Shoubridge, Cheryl, Turner, Rachel, Menzies, Andrew, Maddison, Mark, Hackett, Anna, Barthorpe, Syd, Martinez, Francisco, Turner, Gillian, Parnau, Josef, Jones, David, Vandeleur, Lucianne, Chelly, Jamel, Haan, Eric, Greenman, Chris, Thompson, Deborah, Mohammed, Shehla, Skinner, Cindy, Mironenko, Tatiana, Ropers, Hans-Hilger, Xue, Yali, Field, Michael, Shaw, Marie, Tyler-Smith, Chris, Tolmie, John L, Edkins, Sarah, Pleasance, Erin, Stevenson, Roger E, Schwartz, Charles E, Widaa, Sara, Stephens, Phil, Goliath, Rene, Raynaud, Martine, Easton, Douglas F, Dicks, Ed, Butler, Adam, Raymond, F Lucy, Wray, Paul, Tejada, M Isabel, West, Sofie

“…Tarpey et al . carry out a large-scale systematic sequencing of the majority of X-chromosome coding exons from 208 families with multiple individuals with…”
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Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype by Hiatt, Susan M., Trajkova, Slavica, Sebastiano, Matteo Rossi, Partridge, E. Christopher, Abidi, Fatima E., Anderson, Ashlyn, Ansar, Muhammad, Antonarakis, Stylianos E., Azadi, Azadeh, Bachmann-Gagescu, Ruxandra, Bartuli, Andrea, Benech, Caroline, Berkowitz, Jennifer L., Betti, Michael J., Brusco, Alfredo, Cannon, Ashley, Caron, Giulia, Chen, Yanmin, Cochran, Meagan E., Coleman, Tanner F., Crenshaw, Molly M., Cuisset, Laurence, Curry, Cynthia J., Darvish, Hossein, Demirdas, Serwet, Descartes, Maria, Douglas, Jessica, Dyment, David A., Elloumi, Houda Zghal, Ermondi, Giuseppe, Faoucher, Marie, Farrow, Emily G., Felker, Stephanie A., Fisher, Heather, Hurst, Anna C.E., Joset, Pascal, Kelly, Melissa A., Kmoch, Stanislav, Leadem, Benjamin R., Lyons, Michael J., Macchiaiolo, Marina, Magner, Martin, Mandrile, Giorgia, Mattioli, Francesca, McEown, Megan, Meadows, Sarah K., Medne, Livija, Meeks, Naomi J.L., Montgomery, Sarah, Napier, Melanie P., Natowicz, Marvin, Newberry, Kimberly M., Niceta, Marcello, Noskova, Lenka, Nowak, Catherine B., Noyes, Amanda G., Osmond, Matthew, Prijoles, Eloise J., Pugh, Jada, Pullano, Verdiana, Quélin, Chloé, Rahimi-Aliabadi, Simin, Rauch, Anita, Redon, Sylvia, Reymond, Alexandre, Schwager, Caitlin R., Sellars, Elizabeth A., Scheuerle, Angela E., Shukarova-Angelovska, Elena, Skraban, Cara, Stolerman, Elliot, Sullivan, Bonnie R., Tartaglia, Marco, Thiffault, Isabelle, Uguen, Kevin, Umaña, Luis A., van Bever, Yolande, van der Crabben, Saskia N., van Slegtenhorst, Marjon A., Waisfisz, Quinten, Washington, Camerun, Rodan, Lance H., Myers, Richard M., Cooper, Gregory M.

“…Neurodevelopmental disorders (NDDs) result from highly penetrant variation in hundreds of different genes, some of which have not yet been identified. Using…”
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Molecular Cloning and Characterization of TRPC5 (HTRP5), the Human Homologue of a Mouse Brain Receptor-Activated Capacitative Ca2+ Entry Channel by Sossey-Alaoui, Khalid, Lyon, Jenifer A., Jones, Latonya, Abidi, Fatima E., Hartung, Andrew J., Hane, Bernhard, Schwartz, Charles E., Stevenson, Roger E., Srivastava, Anand K.

“…A novel human gene, TRPC5, was cloned from the region of Xq23 that contains loci for nonsyndromic mental retardation (MRX47 and MRX35) and two genes, DCX and…”
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A systematic review on the use of action research methods in mental health nursing care by Moreno‐Poyato, Antonio R., Subias‐Miquel, Martí, Tolosa‐Merlos, Diana, Ventosa‐Ruiz, Ana, Pérez‐Toribio, Alonso, EL Abidi, Kadhija, Navarro‐Maldonado, Raquel, Suárez‐Pérez, Raquel, Valera‐Fernández, Rosario, Romeu‐Labayen, Maria, Lluch‐Canut, Teresa, Roldán‐Merino, Juan, Puig‐Llobet, Montserrat

“…Aims To identify and synthesize evidence on the use of action research methods in mental health nursing care. Design Systematic review. Data Sources CINAHL,…”
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Angelman syndrome with a 15q11q13 deletion in a mother and daughter by Bell, Shannon, Butler, Kameryn M., Drazba, Kathryn T., Lynch, Jennifer, Abidi, Fatima E., DuPont, Barbara, Stevenson, Roger E.

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A novel 2 bp deletion in the TM4SF2 gene is associated with MRX58 by Abidi, F E, Holinski-Feder, E, Rittinger, O, Kooy, F, Lubs, H A, Stevenson, R E, Schwartz, C E

“…The primers were designed to be approximately 50 bp away from the exon/intron boundary to ensure detection of any alteration at the splice junction. Since the…”
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CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes by HACKETT, Anna, TARPEY, Patrick S, TOLMIE, John, YATES, John Rw, TURNER, Gillian, WILSON, Meredith, FUTREAL, Andrew P, CORBETT, Mark, SHAW, Marie, GECZ, Jozef, RAYMOND, F. Lucy, STRATTON, Michael R, LICATA, Andrea, SCHWARTZ, Charles E, ABIDI, Fatima E, COX, James, WHIBLEY, Annabel, BOYLE, Jackie, ROGERS, Carolyn, GRIGG, John, PARTINGTON, Michael, STEVENSON, Roger E

“…Mutations of the calcium/calmodulin-dependent serine protein kinase (CASK) gene have recently been associated with X-linked mental retardation (XLMR) with…”
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Reduced depression risk in adults undergoing surgical intervention for Obstructive Sleep Apnea: 2-year follow-up cohort by Maciel de Oliveira, C., Abidi, E., Marques, S., Abdelwahab, M., Capasso, R.

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Identification and Characterization of a Phase-Specific, Nuclear DNA Binding Protein from the Dimorphic Pathogenic Fungus Histoplasma capsulatum by ABIDI, F. E, ROH, H, KEATH, E. J

“…Classifications Services IAI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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