Stress and β-carbolines decrease the density of low affinity GABA binding sites; an effect reversed by diazepam von BIGGIO, G, CONCAS, A, SERRA, M, SALIS, M, CORDA, M. G, NURCHI, V, CRISPONI, C, GESSA, G. L

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Stress and β-carbolines decrease the density of low affinity gaba binding sites von Biggio, G., Concas, A., Serra, M., Salis, M., Corda, M.G., Nurchi, V., Crisponi, C., Gessa, G.L.

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Crisponi Syndrome Is Caused by Mutations in the CRLF1 Gene and Is Allelic to Cold-Induced Sweating Syndrome Type 1 von Crisponi, Laura, Crisponi, Giangiorgio, Meloni, Alessandra, Toliat, Mohammad Reza, Nürnberg, Gudrun, Usala, Gianluca, Uda, Manuela, Masala, Marco, Höhne, Wolfgang, Becker, Christian, Marongiu, Mara, Chiappe, Francesca, Kleta, Robert, Rauch, Anita, Wollnik, Bernd, Strasser, Friedrich, Reese, Thomas, Jakobs, Cornelis, Kurlemann, Gerd, Cao, Antonio, Nürnberg, Peter, Rutsch, Frank

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The Role of Magnesium in Pregnancy and in Fetal Programming of Adult Diseases von Fanni, Daniela, Gerosa, C., Nurchi, V. M., Manchia, M., Saba, L., Coghe, F., Crisponi, G., Gibo, Y., Van Eyken, P., Fanos, V., Faa, G.

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Foxl2 is required for commitment to ovary differentiation von Ottolenghi, Chris, Omari, Shakib, Garcia-Ortiz, J. Elias, Uda, Manuela, Crisponi, Laura, Forabosco, Antonino, Pilia, Giuseppe, Schlessinger, David

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Solution studies, synthesis and antibacterial activity of Ga(III) complexes with bis-kojate derivatives von O'Ferrall, L. More, Fantasia, A., Chan, K., Teixeira, L.M., Kavanagh, K., O'Connor, C., Santos, M.A., Chaves, S., Nurchi, V.M., Crisponi, G., Zoroddu, M.A., Griffith, D.M., Cappai, R.

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A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation von Naitza, Silvia, Porcu, Eleonora, Steri, Maristella, Taub, Dennis D, Mulas, Antonella, Xiao, Xiang, Strait, James, Dei, Mariano, Lai, Sandra, Busonero, Fabio, Maschio, Andrea, Usala, Gianluca, Zoledziewska, Magdalena, Sidore, Carlo, Zara, Ilenia, Pitzalis, Maristella, Loi, Alessia, Virdis, Francesca, Piras, Roberta, Deidda, Francesca, Whalen, Michael B, Crisponi, Laura, Concas, Antonio, Podda, Carlo, Uzzau, Sergio, Scheet, Paul, Longo, Dan L, Lakatta, Edward, Abecasis, Gonçalo R, Cao, Antonio, Schlessinger, David, Uda, Manuela, Sanna, Serena, Cucca, Francesco

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Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease von Uusimaa, J, Jungbluth, H, Fratter, C, Crisponi, G, Feng, L, Zeviani, M, Hughes, I, Treacy, E P, Birks, J, Brown, G K, Sewry, C A, McDermott, M, Muntoni, F, Poulton, J

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Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women von Fox, Caroline S, Liu, Yongmei, White, Charles C, Feitosa, Mary, Smith, Albert V, Heard-Costa, Nancy, Lohman, Kurt, Johnson, Andrew D, Foster, Meredith C, Greenawalt, Danielle M, Griffin, Paula, Ding, Jinghong, Newman, Anne B, Tylavsky, Fran, Miljkovic, Iva, Kritchevsky, Stephen B, Launer, Lenore, Garcia, Melissa, Eiriksdottir, Gudny, Carr, J Jeffrey, Gudnason, Vilmunder, Harris, Tamara B, Cupples, L Adrienne, Borecki, Ingrid B

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Hydroxypyridinones with enhanced iron chelating properties. Synthesis, characterization and in vivo tests of 5-hydroxy-2-(hydroxymethyl)pyridine-4(1H)-one von Lachowicz, J I, Nurchi, V M, Crisponi, G, Jaraquemada-Pelaez, M G, Arca, M, Pintus, A, Santos, M A, Quintanova, C, Gano, L, Szewczuk, Z, Zoroddu, M A, Peana, M, Domínguez-Martín, A, Choquesillo-Lazarte, D

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Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report von Alves, Rita Maria, Uva, Paolo, Veiga, Marielza F, Oppo, Manuela, Zschaber, Fabiana C R, Porcu, Giampiero, Porto, Henrique P, Persico, Ivana, Onano, Stefano, Cuccuru, Gianmauro, Atzeni, Rossano, Vieira, Lauro C N, Pires, Marcos V A, Cucca, Francesco, Toralles, Maria Betânia P, Angius, Andrea, Crisponi, Laura

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Aging of Oocyte, Ovary, and Human Reproduction von OTTOLENGHI, CHRIS, UDA, MANUELA, HAMATANI, TOSHIO, CRISPONI, LAURA, GARCIA, JOSE-ELIAS, KO, MINORU, PILIA, GIUSEPPE, SFORZA, CHIARELLA, SCHLESSINGER, DAVID, FORABOSCO, ANTONINO

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Association between Adult Height and Risk of Colorectal, Lung, and Prostate Cancer: Results from Meta-analyses of Prospective Studies and Mendelian Randomization Analyses von Khankari, Nikhil K, Shu, Xiao-Ou, Wen, Wanqing, Kraft, Peter, Lindström, Sara, Peters, Ulrike, Schildkraut, Joellen, Schumacher, Fredrick, Bofetta, Paolo, Risch, Angela, Bickeböller, Heike, Amos, Christopher I, Easton, Douglas, Eeles, Rosalind A, Gruber, Stephen B, Haiman, Christopher A, Hunter, David J, Chanock, Stephen J, Pierce, Brandon L, Zheng, Wei

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Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index von Hinney, A, Kesselmeier, M, Jall, S, Volckmar, A-L, Föcker, M, Antel, J, Heid, I M, Winkler, T W, Grant, S F A, Guo, Y, Bergen, A W, Kaye, W, Berrettini, W, Hakonarson, H, Herpertz-Dahlmann, B, de Zwaan, M, Herzog, W, Ehrlich, S, Zipfel, S, Egberts, K M, Adan, R, Brandys, M, van Elburg, A, Boraska Perica, V, Franklin, C S, Tschöp, M H, Zeggini, E, Bulik, C M, Collier, D, Scherag, A, Müller, T D, Hebebrand, J

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Confirmation of a new phenotype in an individual with a variant in the last part of exon 30 of CREBBP von Angius, Andrea, Uva, Paolo, Oppo, Manuela, Persico, Ivana, Onano, Stefano, Olla, Stefania, Pes, Valentina, Perria, Chiara, Cuccuru, Gianmauro, Atzeni, Rossano, Serra, Gigliola, Cucca, Francesco, Sotgiu, Stefano, Hennekam, Raoul C., Crisponi, Laura

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Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development von Uda, Manuela, Ottolenghi, Chris, Crisponi, Laura, Garcia, Jose Elias, Deiana, Manila, Kimber, Wendy, Forabosco, Antonino, Cao, Antonio, Schlessinger, David, Pilia, Giuseppe

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Investigating the genetic relationship between Alzheimer’s disease and cancer using GWAS summary statistics von Feng, Yen-Chen Anne, Cho, Kelly, Lindstrom, Sara, Kraft, Peter, Cormack, Jean, Liang, Liming, Driver, Jane A.

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p63 Gene Mutations in EEC Syndrome, Limb-Mammary Syndrome, and Isolated Split Hand–Split Foot Malformation Suggest a Genotype-Phenotype Correlation von van Bokhoven, Hans, Hamel, Ben C.J., Bamshad, Mike, Sangiorgi, Eugenio, Gurrieri, Fiorella, Duijf, Pascal H.G., Vanmolkot, Kaate R.J., van Beusekom, Ellen, van Beersum, Sylvia E.C., Celli, Jacopo, Merkx, Gerard F.M., Tenconi, Romano, Fryns, Jean Pierre, Verloes, Alain, Newbury-Ecob, Ruth A., Raas-Rotschild, Annick, Majewski, Frank, Beemer, Frits A., Janecke, Andreas, Chitayat, David, Crisponi, Giangiorgio, Kayserili, Hülya, Yates, John R.W., Neri, Giovanni, Brunner, Han G.

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Interactions of Dietary Whole-Grain Intake With Fasting Glucose- and Insulin-Related Genetic Loci in Individuals of European Descent: A meta-analysis of 14 cohort studies von Nettleton, Jennifer A, McKeown, Nicola M, Kanoni, Stavroula, Lemaitre, Rozenn N, Hivert, Marie-France, Ngwa, Julius, van Rooij, Frank J.A, Sonestedt, Emily, Wojczynski, Mary K, Ye, Zheng, Tanaka, Tosh

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Complex formation equilibria of Cu2+ and Zn2+ with Irbesartan and Losartan von Lachowicz, Joanna I, Nurchi, Valeria M, Crisponi, Guido, Jaraquemada-Pelaez, Maria de Guadalupe, Caltagirone, C, Peana, M, Zoroddu, MA, Szewczuk, Zbigniew, Cooper, Garth

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