PTCH Gene Mutations in Odontogenic Keratocysts von Barreto, D.C., Gomez, R.S., Bale, A.E., Boson, W.L., De Marco, L.

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Clonal composition of human adamantinomatous craniopharyngiomas and somatic mutation analyses of the patched ( PTCH), Gsα and Gi2α genes von Sarubi, J.C., Bei, H., Adams, E.F., Boson, W.L., Friedman, E., Brandão, K., Kalapothakis, E., Miranda, D., Valle, F.L., Sarquis, M.S., De Marco, L.

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Naturally occurring antibacterial activities of avian and crocodile tissues von Shaharabany, M, Gollop, N, Ravin, S, Golomb, E, DeMarco, L, Ferreira, P C, Boson, W L, Friedman, E

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p.F508del in a heterogeneous cystic fibrosis population from Minas Gerais, Brazil von Vidigal, P V T, Reis, F J C, Boson, W L M, De Marco, L A, Brasileiro-Filho, G

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Nephrogenic Diabetes Insipidus: An X Chromosome-Linked Dominant Inheritance Pattern with a Vasopressin Type 2 Receptor Gene that is Structurally Normal von Friedman, Eitan, Bale, Allen E., Carson, Emma, Boson, Wolfanga L., Nordenskjöld, Magnus, Ritzén, Martin, Ferreira, Paulo C., Jammal, Anibal, De Marco, Luiz

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Investigation of A218C tryptophan hydroxylase polymorphism: association with familial suicide behavior and proband's suicide attempt characteristics von Viana, M. M., De Marco, L. A., Boson, W. L., Romano‐Silva, M. A., Corrêa, H.

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Mutational Analyses of Candidate Genes in Human Squamous Cell Carcinomas von Petroianu, Andy, Boson, Wolfanga L., Bale, Allen E., Friedman, Eitan, De Marco, Luiz

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Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gsα gene von DEMARCO, L, STRATAKIS, C. A, FRIEDMAN, E, BOSON, W. L, JAKBOVITZ, O, CARSON, E, ANDRADE, L. M, AMARAL, V. F, ROCHA, J. L, CHOURSOS, G. P, NORDENSKJÖLD, M

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Thiopurine methyltransferase polymorphisms in a Brazilian population von Boson, W L, Romano-Silva, M A, Correa, H, Falcão, R P, Teixeira-Vidigal, P V, De Marco, L

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Microsatellite instability in sporadic parathyroid adenoma von Sarquis, M, Friedman, E, Boson, W L, Gomez, R S, Dias, A F, De Marco, L

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A Novel Mutation of the Cathepsin C Gene in Papillon-Lefévre Syndrome von Cury, Vanessa F, Costa, José E, Gomez, Ricardo S, Boson, Wolfanga L, Loures, Cyro G, De Marco, Luiz

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A signal peptide mutation of the arginine vasopressin gene in monozygotic twins von Boson, Wolfanga L., Sarubi, Juliana C., D’Alva, Catarina B., Friedman, Eitan, Faria, Daniela, De Marco, Luiz, Wajchenberg, Bernardo

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Clonal composition of human adamantinomatous craniopharyngiomas and somatic mutation analyses of the patched (PTCH), Gsalpha and Gi2alpha genes von Sarubi, J C, Bei, H, Adams, E F, Boson, W L, Friedman, E, Brandão, K, Kalapothakis, E, Miranda, D, Valle, F L, Sarquis, M S, De Marco, L

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Micro satellite instability in sporadic parathyroid adenoma von SARQUIS, M, FRIEDMAN, E, BOSON, W. L, GOMEZ, R. S, DIAS, A. F, DE MARCO, L

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Search for charged Higgs bosons: combined results using LEP data von Abbiendi, G., Ainsley, C., Akesson, P.F., Alexander, G., Anagnostou, G., Anderson, K.J., Asai, S., Axen, D., Bailey, I., Barberio, E., Barillari, T., Barlow, R.J., Batley, R.J., Bechtle, P., Behnke, T., Bell, K.W., Bell, P.J., Bella, G., Bellerive, A., Benelli, G., Bethke, S., Biebel, O., Boeriu, O., Bock, P., Boutemeur, M., Braibant, S., Brown, R.M., Burckhart, H.J., Campana, S., Capiluppi, P., Carnegie, R.K., Carter, A.A., Carter, J.R., Chang, C.Y., Charlton, D.G., Ciocca, C., Csilling, A., Cuffiani, M., Dado, S., Dallavalle, M., de Roeck, A., de Wolf, E.A., Desch, K., Dienes, B., Dubbert, J., Duchovni, E., Duckeck, G., Duerdoth, I.P., Etzion, E., Fabbri, F., Ferrari, P., Fiedler, F., Fleck, I., Ford, M., Frey, A., Gagnon, P., Geich-Gimbel, C., Giacomelli, G., Giacomelli, P., Giunta, M., Goldberg, J., Gross, E., Grunhaus, J., Gruwe, M., Gupta, Anupam, Hajdu, C., Hamann, M., Hanson, G.G., Harel, A., Hauschild, M., Hawkes, C.M., Hawkings, R., Herten, G., Heuer, R.D., Hill, J.C., Horvath, Dragos, Igo-Kemenes, P., Ishii, K., Jeremie, H., Jovanovic, P., Junk, T.R., Kanzaki, J., Karlen, D., Kawagoe, K., Kawamoto, T., Keeler, R.K., Kellogg, R.G., Kennedy, B.W., Kluth, S., Kobayashi, T., Kobel, M., Komamiya, S., Kramer, T., Krasznahorkay, A., Krieger, P., von Krogh, J., Kuhl, T., Kupper, M., Lafferty, G.D., Landsman, H.

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Search for the Standard Model Higgs boson at LEP von Lep Higgs Working Group For Higgs Boson, Searches

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Lentiviral vectors pseudotyped with a modified RD114 envelope glycoprotein show increased stability in sera and augmented transduction of primary lymphocytes and CD34+ cells derive... von Sandrin, Virginie, Boson, Bertrand, Salmon, Patrick, Gay, Wilfried, Nègre, Didier, Le Grand, Roger, Trono, Didier, Cosset, François-Loı̈c

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Important Role for the Transmembrane Domain of Severe Acute Respiratory Syndrome Coronavirus Spike Protein during Entry von BROER, Rene, BOSON, Bertrand, SPAAN, Willy, COSSET, Francois-Loïc, CORVER, Jeroen

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Association of the serotonin transporter promoter polymorphism with suicidal behavior von Campi-Azevedo, A C, Boson, W, De Marco, L, Romano-Silva, M A, Correa, H

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A homozygous cathepsin C mutation associated with Haim–Munk syndrome von Cury, V.F., Gomez, R.S., Costa, J.E., Friedman, E., Boson, W., De Marco, L.

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