Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure von Li, Duanxiang, Parks, Sharie B., Kushner, Jessica D., Nauman, Deirdre, Burgess, Donna, Ludwigsen, Susan, Partain, Julie, Nixon, Randal R., Allen, Charles N., Irwin, Robert P., Jakobs, Petra M., Litt, Michael, Hershberger, Ray E.

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ERCC1 is required for FANCD2 focus formation von McCabe, Kevin M., Hemphill, Aaron, Akkari, Yassmine, Jakobs, Petra M., Pauw, Daniel, Olson, Susan B., Moses, Robb E., Grompe, Markus

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A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation von Hershberger, Ray E., Hanson, Emily L., Jakobs, Petra M., Keegan, Hugh, Coates, Kelly, Bousman, Sylvia, Litt, Michael

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Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia von Lensch, M. William, Tischkowitz, Marc, Christianson, Tracy A., Reifsteck, Carol A., Speckhart, S. Ashley, Jakobs, Petra M., O’Dwyer, Michael E., Olson, Susan B., Le Beau, Michelle M., Hodgson, Shirley V., Mathew, Christopher G., Larson, Richard A., Bagby, Grover C.

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Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy von Hanson, Emily L., Jakobs, Petra M., Keegan, Hugh, Coates, Kelly, Bousman, Sylvia, Dienel, Nicholas H., Litt, Michael, Hershberger, Ray E.

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Role for DNA Polymerase κ in the Processing of N2-N2-Guanine Interstrand Cross-links von Minko, Irina G., Harbut, Michael B., Kozekov, Ivan D., Kozekova, Albena, Jakobs, Petra M., Olson, Susan B., Moses, Robb E., Harris, Thomas M., Rizzo, Carmelo J., Lloyd, R. Stephen

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Autosomal-Dominant Congenital Cataract Associated with a Deletion Mutation in the Human Beaded Filament Protein Gene BFSP2 von Jakobs, Petra M., Hess, John F., FitzGerald, Paul G., Kramer, Patricia, Weleber, Richard G., Litt, Michael

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Embryonic stem cells can be used to construct hybrid cell lines containing a single, selectable murine chromosome von Jakobs, P M, Smith, L, Thayer, M, Grompe, M

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Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease von Jakobs, Petra M., Hanson, Emily L., Crispell, Kathy A., Toy, Warren, Keegan, Hugh, Schilling, Karla, Icenogle, Timothy B., Litt, Michael, Hershberger, Ray E.

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Role for DNA Polymerase Kappa in the Processing of N super(2)-N super(2)-Guanine Interstrand Cross-links von Minko, Irina G, Harbut, Michael B, Kozekov, Ivan D, Kozekova, Albena, Jakobs, Petra M, Olson, Susan B, Moses, Robb E, Harris, Thomas M, Rizzo, Carmelo J, Lloyd, RStephen

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Role for DNA Polymerase κ in the Processing of N2-N2-Guanine Interstrand Cross-links von Irina G. Minko, Michael B. Harbut, Ivan D. Kozekov, Albena Kozekova, Petra M. Jakobs, Susan B. Olson, Robb E. Moses, Thomas M. Harris, Carmelo J. Rizzo, R. Stephen Lloyd

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Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p von Whitney, Michael, Thayer, Matt, Reifsteck, Carol, Olson, Susan, Smith, Leslie, Jakobs, Petra M., Leach, Robin, Naylor, Susan, Joenje, Hans, Grompe, Markus

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A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews von Whitney, Michael A., Saito, Hiroshi, Jakobs, Petra M., Gibson, Rachel A., Moses, Robb E., Grompe, Markus

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Localization of the Fanconi Anemia Complementation Group D Gene to a 200-kb Region on Chromosome 3p25.3 von Hejna, James A., Timmers, Cynthia D., Reifsteck, Carol, Bruun, Donald A., Lucas, Lora W., Jakobs, Petra M., Toth-Fejel, SuEllen, Unsworth, Nancy, Clemens, Susan L., Garcia, Dawn K., Naylor, Susan L., Thayer, Mathew J., Olson, Susan B., Grompe, Markus, Moses, Robb E.

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A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation. Editorial von HERSHBERGER, Ray E, HANSON, Emlly L, JAKOBS, Petra M, KEEGAN, Hugh, COATES, Kelly, BOUSMAN, Sylvia, LITT, Michael, DONAHUE, Mark, KRAUS, William, GRANGER, Christophe

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Cloning and Characterization of a Human cDNA (INPPL1) Sharing Homology with Inositol Polyphosphate Phosphatases von Hejna, James A., Saito, Hiroshi, Merkens, Louise S., Tittle, Thomas V., Jakobs, Petra M., Whitney, Michael A., Grompe, Markus, Friedberg, Andrew S., Moses, Robb E.

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Fanconi anemia cells have a normal gene structure for topoisomerase I von SAITO, H, GROMPE, M, NEELEY, T. L, JAKOBS, P. M, MOSES, R. E

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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection von Pardiñas, Antonio F., Holmans, Peter, Pocklington, Andrew J., Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Esben, Als, Thomas D., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bøcker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Pedersen, Marianne Giørtz, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Hansen, Christine Søholm, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael J., O’Donovan, Michael C., Walters, James T. R.

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Eltrombopag Added to Immunosuppression in Severe Aplastic Anemia von Peffault de Latour, Régis, Kulasekararaj, Austin, Iacobelli, Simona, Terwel, Sofie R, Cook, Riley, Griffin, Morag, Halkes, Constantijn J.M, Recher, Christian, Barraco, Fiorenza, Forcade, Edouard, Vallejo, Juan-Carlos, Drexler, Beatrice, Mear, Jean-Baptiste, Smith, Alexander E, Angelucci, Emanuele, Raymakers, Reinier A.P, de Groot, Marco R, Daguindau, Etienne, Nur, Erfan, Barcellini, Wilma, Russell, Nigel H, Terriou, Louis, Iori, Anna-Paola, La Rocca, Ursula, Sureda, Anna, Sánchez-Ortega, Isabel, Xicoy, Blanca, Jarque, Isidro, Cavenagh, James, Sicre de Fontbrune, Flore, Marotta, Serena, Munir, Talha, Tjon, Jennifer M.L, Tavitian, Suzanne, Praire, Aline, Clement, Laurence, Rabian, Florence, Marano, Luana, Hill, Anita, Palmisani, Elena, Muus, Petra, Cacace, Fabiana, Frieri, Camilla, van Lint, Maria-Teresa, Passweg, Jakob R, Marsh, Judith C.W, Socié, Gérard, Mufti, Ghulam J, Dufour, Carlo, Risitano, Antonio M

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Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy von Parks, Sharie B., PhD, Kushner, Jessica D., MS, CGC, Nauman, Deirdre, BSN, Burgess, Donna, BSN, Ludwigsen, Susan, MA, Peterson, Amanda, BS, Li, Duanxiang, MD, Jakobs, Petra, PhD, Litt, Michael, PhD, Porter, Charles B., MD, FACC, Rahko, Peter S., MD, FACC, Hershberger, Ray E., MD, FACC

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