The Practice of Politics: The English Civil War and the ‘Resolution’ of Henrietta Maria and Charles I von Bulman, William J.

Volltext

Lithographing Trade, The von Bulman, W J

Volltext

Heritability of chromosomal radiosensitivity in breast cancer patients: a pilot study with the lymphocyte micronucleus assay von Burrill, J. B. P. Barber, S. A. Roberts, B. Bulman, D. Scott, W.

Volltext

Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care von Sawyer, S.L., Hartley, T., Dyment, D.A., Beaulieu, C.L., Schwartzentruber, J., Smith, A., Bedford, H.M., Bernard, G., Bernier, F.P., Brais, B., Bulman, D.E., Warman Chardon, J., Chitayat, D., Deladoëy, J., Fernandez, B.A., Frosk, P., Geraghty, M.T., Gerull, B., Gibson, W., Gow, R.M., Graham, G.E., Green, J.S., Heon, E., Horvath, G., Innes, A.M., Jabado, N., Kim, R.H., Koenekoop, R.K., Khan, A., Lehmann, O.J., Mendoza-Londono, R., Michaud, J.L., Nikkel, S.M., Penney, L.S., Polychronakos, C., Richer, J., Rouleau, G.A., Samuels, M.E., Siu, V.M., Suchowersky, O., Tarnopolsky, M.A., Yoon, G., Zahir, F.R., Majewski, J., Boycott, K.M.

Volltext

Systematic Analysis of Mobile Genetic Elements Mediating β-Lactamase Gene Amplification in Noncarbapenemase-Producing Carbapenem-Resistant Enterobacterales Bloodstream Infections von Shropshire, W C, Konovalova, A, McDaneld, P, Gohel, M, Strope, B, Sahasrabhojane, P, Tran, C N, Greenberg, D, Kim, J, Zhan, X, Aitken, S, Bhatti, M, Savidge, T C, Treangen, T J, Hanson, B M, Arias, C A, Shelburne, S A

Volltext

Whole-exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study von Dyment, D.A., Tétreault, M., Beaulieu, C.L., Hartley, T., Ferreira, P., Chardon, J.W., Marcadier, J., Sawyer, S.L., Mosca, S.J., Innes, A.M., Parboosingh, J.S., Bulman, D.E., Schwartzentruber, J., Majewski, J., Tarnopolsky, M., Boycott, K.M.

Volltext

Addresses by Citizens to School Boys [Concluded] von Simpson, R. M., Fetherstonhaugh, E. P., Bury, George, Bulman, W. J.

Volltext

XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia von Hoch, Nicolas C., Hanzlikova, Hana, Rulten, Stuart L., Tétreault, Martine, Komulainen, Emilia, Ju, Limei, Hornyak, Peter, Zeng, Zhihong, Gittens, William, Rey, Stephanie A., Staras, Kevin, Mancini, Grazia M. S., McKinnon, Peter J., Wang, Zhao-Qi, Wagner, Justin D., Yoon, Grace, Caldecott, Keith W.

Volltext

N -Acyloxymethyl-phthalimides deliver genotoxic formaldehyde to human cells von Emms, Vicki L, Lewis, Liam A, Beja, Lilla, Bulman, Natasha F A, Pires, Elisabete, Muskett, Frederick W, McCullagh, James S O, Swift, Lonnie P, McHugh, Peter J, Hopkinson, Richard J

Volltext

Technology and Education: Computers, Software, and the Internet

Volltext

Voluntary Running Triggers VGF-Mediated Oligodendrogenesis to Prolong the Lifespan of Snf2h-Null Ataxic Mice von Alvarez-Saavedra, Matías, De Repentigny, Yves, Yang, Doo, O’Meara, Ryan W., Yan, Keqin, Hashem, Lukas E., Racacho, Lemuel, Ioshikhes, Ilya, Bulman, Dennis E., Parks, Robin J., Kothary, Rashmi, Picketts, David J.

Volltext

Action spectroscopy of the isolated red Kaede fluorescent protein chromophore von Coughlan, Neville J. A., Stockett, Mark H., Kjær, Christina, Ashworth, Eleanor K., Bulman Page, Philip C., Meech, Stephen R., Brøndsted Nielsen, Steen, Blancafort, Lluís, Hopkins, W. Scott, Bull, James N.

Volltext

Haploinsufficiency of a Spliceosomal GTPase Encoded by EFTUD2 Causes Mandibulofacial Dysostosis with Microcephaly von Lines, Matthew A., Huang, Lijia, Schwartzentruber, Jeremy, Douglas, Stuart L., Lynch, Danielle C., Beaulieu, Chandree, Guion-Almeida, Maria Leine, Zechi-Ceide, Roseli Maria, Gener, Blanca, Gillessen-Kaesbach, Gabriele, Nava, Caroline, Baujat, Geneviève, Horn, Denise, Kini, Usha, Caliebe, Almuth, Alanay, Yasemin, Utine, Gulen Eda, Lev, Dorit, Kohlhase, Jürgen, Grix, Arthur W., Lohmann, Dietmar R., Hehr, Ute, Böhm, Detlef, Majewski, Jacek, Bulman, Dennis E., Wieczorek, Dagmar, Boycott, Kym M.

Volltext

Mutations in LAMA1 Cause Cerebellar Dysplasia and Cysts with and without Retinal Dystrophy von Aldinger, Kimberly A., Mosca, Stephen J., Tétreault, Martine, Dempsey, Jennifer C., Ishak, Gisele E., Hartley, Taila, Phelps, Ian G., Lamont, Ryan E., O’Day, Diana R., Basel, Donald, Gripp, Karen W., Baker, Laura, Stephan, Mark J., Bernier, Francois P., Boycott, Kym M., Majewski, Jacek, Parboosingh, Jillian S., Innes, A. Micheil, Doherty, Dan

Volltext

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4 von Ophoff, R A, Terwindt, G M, Vergouwe, M N, van Eijk, R, Oefner, P J, Hoffman, S M, Lamerdin, J E, Mohrenweiser, H W, Bulman, D E, Ferrari, M, Haan, J, Lindhout, D, van Ommen, G J, Hofker, M H, Ferrari, M D, Frants, R R

Volltext

Effect of Endobronchial Coils vs Usual Care on Exercise Tolerance in Patients With Severe Emphysema: The RENEW Randomized Clinical Trial von Sciurba, Frank C, Criner, Gerard J, Strange, Charlie, Shah, Pallav L, Michaud, Gaetane, Connolly, Timothy A, Deslée, Gaëtan, Tillis, William P, Delage, Antoine, Marquette, Charles-Hugo, Krishna, Ganesh, Kalhan, Ravi, Ferguson, J. Scott, Jantz, Michael, Maldonado, Fabien, McKenna, Robert, Majid, Adnan, Rai, Navdeep, Gay, Steven, Dransfield, Mark T, Angel, Luis, Maxfield, Roger, Herth, Felix J. F, Wahidi, Momen M, Mehta, Atul, Slebos, Dirk-Jan

Volltext

De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes von Rivière, Jean-Baptiste, Mirzaa, Ghayda M, O'Roak, Brian J, Beddaoui, Margaret, Alcantara, Diana, Conway, Robert L, St-Onge, Judith, Schwartzentruber, Jeremy A, Gripp, Karen W, Nikkel, Sarah M, Worthylake, Thea, Sullivan, Christopher T, Ward, Thomas R, Butler, Hailly E, Kramer, Nancy A, Albrecht, Beate, Armour, Christine M, Armstrong, Linlea, Caluseriu, Oana, Cytrynbaum, Cheryl, Drolet, Beth A, Innes, A Micheil, Lauzon, Julie L, Lin, Angela E, Mancini, Grazia M S, Meschino, Wendy S, Reggin, James D, Saggar, Anand K, Lerman-Sagie, Tally, Uyanik, Gökhan, Weksberg, Rosanna, Zirn, Birgit, Beaulieu, Chandree L, Majewski, Jacek, Bulman, Dennis E, O'Driscoll, Mark, Shendure, Jay, Graham, John M, Boycott, Kym M, Dobyns, William B

Volltext

Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial von Burn, John, Prof Sir, Gerdes, Anne-Marie, Prof, Macrae, Finlay, Prof, Mecklin, Jukka-Pekka, Prof, Moeslein, Gabriela, MD, Olschwang, Sylviane, MD, Eccles, Diane, Prof, Evans, D Gareth, Prof, Maher, Eamonn R, Prof, Bertario, Lucio, MD, Bisgaard, Marie-Luise, MD, Dunlop, Malcolm G, Prof, Ho, Judy WC, MD, Hodgson, Shirley V, Prof, Lindblom, Annika, Prof, Lubinski, Jan, Prof, Morrison, Patrick J, Prof, Murday, Victoria, MD, Ramesar, Raj, Prof, Side, Lucy, MD, Scott, Rodney J, Prof, Thomas, Huw JW, Prof, Vasen, Hans F, Prof, Barker, Gail, Crawford, Gillian, Elliott, Faye, Movahedi, Mohammad, PhD, Pylvanainen, Kirsi, Wijnen, Juul T, PhD, Fodde, Riccardo, Prof, Lynch, Henry T, Prof, Mathers, John C, Prof, Bishop, D Timothy, Prof

Volltext

Specific combination of compound heterozygous mutations in 17β-hydroxysteroid dehydrogenase type 4 (HSD17B4) defines a new subtype of D-bifunctional protein deficiency von McMillan, Hugh J, Worthylake, Thea, Schwartzentruber, Jeremy, Gottlieb, Chloe C, Lawrence, Sarah E, Mackenzie, Alex, Beaulieu, Chandree L, Mooyer, Petra A W, Wanders, Ronald J A, Majewski, Jacek, Bulman, Dennis E, Geraghty, Michael T, Ferdinandusse, Sacha, Boycott, Kym M

Volltext

Dothistroma needle blight, weather and possible climatic triggers for the disease's recent emergence von Woods, A. J., Martín-García, J., Bulman, L., Vasconcelos, M. W., Boberg, J., La Porta, N., Peredo, H., Vergara, G., Ahumada, R., Brown, A., Diez, J. J.

Volltext