De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome von Rivière, Jean-Baptiste, van Bon, Bregje W M, Hoischen, Alexander, Kholmanskikh, Stanislav S, O'Roak, Brian J, Gilissen, Christian, Gijsen, Sabine, Sullivan, Christopher T, Christian, Susan L, Abdul-Rahman, Omar A, Atkin, Joan F, Chassaing, Nicolas, Drouin-Garraud, Valerie, Fry, Andrew E, Fryns, Jean-Pierre, Gripp, Karen W, Kempers, Marlies, Kleefstra, Tjitske, Mancini, Grazia M S, Nowaczyk, Małgorzata J M, van Ravenswaaij-Arts, Conny M A, Roscioli, Tony, Marble, Michael, Rosenfeld, Jill A, Siu, Victoria M, de Vries, Bert B A, Shendure, Jay, Verloes, Alain, Veltman, Joris A, Brunner, Han G, Ross, M Elizabeth, Pilz, Daniela T, Dobyns, William B

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De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome von Mirzaa, Ghayda M, Parry, David A, Fry, Andrew E, Giamanco, Kristin A, Schwartzentruber, Jeremy, Vanstone, Megan, Logan, Clare V, Roberts, Nicola, Johnson, Colin A, Singh, Shawn, Kholmanskikh, Stanislav S, Adams, Carissa, Hodge, Rebecca D, Hevner, Robert F, Bonthron, David T, Braun, Kees P J, Faivre, Laurence, Rivière, Jean-Baptiste, St-Onge, Judith, Gripp, Karen W, Mancini, Grazia M S, Pang, Ki, Sweeney, Elizabeth, van Esch, Hilde, Verbeek, Nienke, Wieczorek, Dagmar, Steinraths, Michelle, Majewski, Jacek, Boycott, Kym M, Pilz, Daniela T, Ross, M Elizabeth, Dobyns, William B, Sheridan, Eamonn G

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Disregulated RhoGTPases and Actin Cytoskeleton Contribute to the Migration Defect in Lis1-Deficient Neurons von Kholmanskikh, Stanislav S, Dobrin, Joseph S, Wynshaw-Boris, Anthony, Letourneau, Paul C, Ross, M. Elizabeth

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Calcium-dependent interaction of Lis1 with IQGAP1 and Cdc42 promotes neuronal motility von Ross, M Elizabeth, Kholmanskikh, Stanislav S, Koeller, Hajira B, Wynshaw-Boris, Anthony, Gomez, Timothy, Letourneau, Paul C

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Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome von Vabres, Pierre, Sorlin, Arthur, Kholmanskikh, Stanislav S., Demeer, Bénédicte, St-Onge, Judith, Duffourd, Yannis, Kuentz, Paul, Courcet, Jean-Benoît, Carmignac, Virginie, Garret, Philippine, Bessis, Didier, Boute, Odile, Bron, Alain, Captier, Guillaume, Carmi, Esther, Devauchelle, Bernard, Geneviève, David, Gondry-Jouet, Catherine, Guibaud, Laurent, Lafon, Arnaud, Mathieu-Dramard, Michèle, Thevenon, Julien, Dobyns, William B., Bernard, Geneviève, Polubothu, Satyamaanasa, Faravelli, Francesca, Kinsler, Veronica A., Thauvin, Christel, Faivre, Laurence, Ross, M. Elizabeth, Rivière, Jean-Baptiste

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Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome von Vabres, Pierre, Sorlin, Arthur, Kholmanskikh, Stanislav S., Demeer, Bénédicte, St-Onge, Judith, Duffourd, Yannis, Kuentz, Paul, Courcet, Jean-Benoît, Carmignac, Virginie, Garret, Philippine, Bessis, Didier, Boute, Odile, Bron, Alain, Captier, Guillaume, Carmi, Esther, Devauchelle, Bernard, Geneviève, David, Gondry-Jouet, Catherine, Guibaud, Laurent, Lafon, Arnaud, Mathieu-Dramard, Michèle, Thevenon, Julien, Dobyns, William B., Bernard, Geneviève, Polubothu, Satyamaanasa, Faravelli, Francesca, Kinsler, Veronica A., Thauvin, Christel, Faivre, Laurence, Ross, M. Elizabeth, Rivière, Jean-Baptiste

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794 Postzygotic dominant-negative mutations of RHOA cause a mosaic neuroectodermal syndrome von Vabres, P., Sorlin, A., Kholmanskikh, S., Duffourd, Y., Kuentz, P., Carmignac, V., Bessis, D., Dobyns, W., Polubothu, S., Faravelli, F., Kinsler, V., Faivre, L., Ross, M., Rivière, J.

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Policy brief of the Belgian Europe's Beating Cancer Plan mirror group: children, adolescents and young adults with cancer von Poirel, Hélène A, Schittecatte, Gabrielle, Van Aelst, Fabienne

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Challenges Affecting Listening Comprehension in Professionally-Oriented English and the Strategies for Improvement (Railway Engineering) von Kholmanskikh, Yulia S., Bogatyreva, Inessa Yu

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Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome von Vabres, Pierre, Sorlin, Arthur, Kholmanskikh, Stanislav S., Demeer, Bénédicte, St-Onge, Judith, Duffourd, Yannis, Kuentz, Paul, Courcet, Jean-Benoît, Carmignac, Virginie, Garret, Philippine, Bessis, Didier, Boute, Odile, Bron, Alain, Captier, Guillaume, Carmi, Esther, Devauchelle, Bernard, Geneviève, David, Gondry-Jouet, Catherine, Guibaud, Laurent, Lafon, Arnaud, Mathieu-Dramard, Michèle, Thevenon, Julien, Dobyns, William B., Bernard, Geneviève, Polubothu, Satyamaanasa, Faravelli, Francesca, Kinsler, Veronica A., Thauvin, Christel, Faivre, Laurence, Ross, M. Elizabeth, Rivière, Jean-Baptiste

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De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome von Rivière, Jean-Baptiste, van Bon, Bregje W.M, Hoischen, Alexander, Kholmanskikh, Stanislav S, O'Roak, Brian J, Gilissen, Christian, Gijsen, Sabine, Sullivan, Christopher T, Christian, Susan L, Abdul-Rahman, Omar A, Atkin, Joan F, Chassaing, Nicolas, Drouin-Garraud, Valerie, Fry, Andrew E, Fryns, Jean-Pierre, Gripp, Karen W, Kempers, Marlies, Kleefstra, Tjitske, Mancini, Grazia M.S, Nowaczyk, Małgorzata J.M, van Ravenswaaij-Arts, Conny M.A, Roscioli, Tony, Marble, Michael, Rosenfeld, Jill A, Siu, Victoria M, de Vries, Bert B.A, Shendure, Jay, Verloes, Alain, Veltman, Joris A, Brunner, Han G, Ross, M. Elizabeth, Pilz, Daniela T, Dobyns, William B

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Training of mice in the Y maze using drinking reinforcement and aversive olfactory signal: Facilitatory effect of ginsenosides von Chepurnov, S. A., Chepurnova, N. E., Kholmanskikh, S. S., Berdiev, R. K., Park, J. K., Sohn, Jae-Oh

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Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome von Vabres, P, Sorlin, A, Kholmanskikh, SS, Demeer, B, St-Onge, J, Duffourd, Y, Kuentz, P, Courcet, J-B, Carmignac, V, Garret, P, Bessis, D, Boute, O, Bron, A, Captier, G, Carmi, E, Devauchelle, B, Genevieve, D, Gondry-Jouet, C, Guibaud, L, Lafon, A, Mathieu-Dramard, M, Thevenon, J, Dobyns, WB, Bernard, G, Polubothu, S, Faravelli, F, Kinsler, VA, Thauvin, C, Faivre, L, Ross, ME, Riviere, J-B

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INDEXING DEVICE von KHOLMANSKIKH VYACHESLAV V,SU, KHOLMANSKIKH VASILIJ P,SU, KHOLMANSKIKH LEV V,SU

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De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome von Mirzaa, GM, Parry, DA, Fry, AE, Giamanco, KA, Schwartzentruber, J, Vanstone, M, Logan, CV, Roberts, N, Johnson, CA, Singh, S, Kholmanskikh, SS, Adams, C, Hodge, RD, Hevner, RF, Bonthron, DT, Braun, KPJ, Faivre, L, Rivière, J-B, St-Onge, J, Gripp, KW, Mancini, GMS, Pang, K, Sweeney, E, Van Esch, H, Verbeek, N, Wieczorek, D, Steinraths, M, Majewski, J, FORGE Canada Consortium, Boycott, KM, Pilz, DT, Ross, ME, Dobyns, WB, Sheridan, EG

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Evaluation of the Idle time of Single-Chain and Double-Chain Overhead Power Lines of 6–10 kV by Methods of Queuing Theory von Basmanov, V.G., Kholmanskikh, V.M.

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Activation of RhoC by regulatory ubiquitination is mediated by LNX1 and suppressed by LIS1 von Kholmanskikh, Stanislav, Singh, Shawn, Ross, M. Elizabeth

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Oncology phase I trial design and conduct: time for a change - MDICT Guidelines 2022 von Araujo, D., Greystoke, A., Bates, S., Bayle, A., Calvo, E., Castelo-Branco, L., de Bono, J., Drilon, A., Garralda, E., Ivy, P., Kholmanskikh, O., Melero, I., Pentheroudakis, G., Petrie, J., Plummer, R., Ponce, S., Postel-Vinay, S., Siu, L., Spreafico, A., Stathis, A., Steeghs, N., Yap, C., Yap, T.A., Ratain, M., Seymour, L.

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Testing dilemmas in the clinic: Lessons learned from biomarker-based drug development von Barjesteh van Waalwijk van Doorn-Khosrovani, Sahar, Kholmanskikh Van Criekingen, Olga, Koole, Simone, Thomas, David M., Gelderblom, Hans

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Features of Forecasting Reliability of 6—10 kV Overhead Electric Lines According to Statistics of Their Failures and Reconditionings von Basmanov, Vladislav, Kholmanskikh, Valerii

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