ATM-dependent phosphorylation of nibrin in response to radiation exposure von Khanna, KumKum, Gatei, Magtouf, Young, David, Cerosaletti, Karen M, Desai-Mehta, Ami, Spring, Kevin, Kozlov, Sergei, Lavin, Martin F, Gatti, Richard A, Concannon, Patrick

Volltext

DNA Ligase IV Mutations Identified in Patients Exhibiting Developmental Delay and Immunodeficiency von O'Driscoll, Mark, Cerosaletti, Karen M., Girard, Pierre-M, Dai, Yan, Stumm, Markus, Kysela, Boris, Hirsch, Betsy, Gennery, Andrew, Palmer, Susan E., Seidel, Jörg, Gatti, Richard A., Varon, Raymonda, Oettinger, Marjorie A., Neitzel, Heidemarie, Jeggo, Penny A., Concannon, Patrick

Volltext

Distinct Functional Domains of Nibrin Mediate Mre11 Binding, Focus Formation, and Nuclear Localization von Desai-Mehta, A, Cerosaletti, K M, Concannon, P

Volltext

Retroviral expression of the NBS1 gene in cultured Nijmegen breakage syndrome cells restores normal radiation sensitivity and nuclear focus formation von Cerosaletti, Karen M., Desai-Mehta, Ami, Yeo, Tiong Chia, Kraakman-van der Zwet, Maria, Zdzienicka, Malgorzata Z., Concannon, Patrick

Volltext

Nibrin Forkhead-associated Domain and Breast Cancer C-terminal Domain Are Both Required for Nuclear Focus Formation and Phosphorylation von Cerosaletti, Karen M., Concannon, Patrick

Volltext

Fine Localization of the Nijmegen Breakage Syndrome Gene to 8q21: Evidence for a Common Founder Haplotype von Cerosaletti, Karen M., Lange, Ethan, Stringham, Heather M., Weemaes, Corry M.R., Smeets, Dominique, Sölder, B., Belohradsky, B.H., Taylor, A. Malcolm R., Karnes, Pamela, Elliott, Alison, Komatsu, Kenshi, Gatti, Richard A., Boehnke, Michael, Concannon, Pat

Volltext

Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome von Varon, Raymonda, Vissinga, Christine, Platzer, Matthias, Cerosaletti, Karen M, Chrzanowska, Krystyna H, Saar, Kathrin, Beckmann, Georg, Seemanová, Eva, Cooper, Paul R, Nowak, Norma J, Stumm, Markus, Weemaes, Corry M.R, Gatti, Richard A, Wilson, Richard K, Digweed, Martin, Rosenthal, André, Sperling, Karl, Concannon, Patrick, Reis, André

Volltext

Identification of the Human βA2 Crystallin Gene ( CRYBA2): Localization of the Gene on Human Chromosome 2 and of the Homologous Gene on Mouse Chromosome 1 von Hulsebos, T.J.M., Cerosaletti, K.M., Fournier, R.E.K., Sinke, R.J., Rocchi, M., Marzella, R., Jenkins, N.A., Gilbert, D.J., Copeland, N.G.

Volltext

Functional delivery of large genomic DNA to human cells with a peptide-lipid vector von White, Robert E., Wade-Martins, Richard, Hart, Stephen L., Frampton, Jon, Huey, Bryan, Desai-Mehta, Ami, Cerosaletti, Karen M., Concannon, Patrick, James, Michael R.

Volltext

Mutations and molecular variants of the NBS1 gene in non-Hodgkin lymphoma von Cerosaletti, Karen M., Morrison, V. Anne, Sabath, Daniel E., Willerford, Dennis M., Concannon, Patrick

Volltext

The Gene for the Serpin Thrombin Inhibitor (P17), Protease Nexin I, Is Located on Human Chromosome 2q33-q35 and on Syntenic Regions in the Mouse and Sheep Genomes von Carter, Royston E., Cerosaletti, Karen M., Burkin, Dean J., Fournier, R.E.K., Jones, Carol, Greenberg, Barry D., Citron, Bruce A., Festoff, Barry W.

Volltext

Extinction of Albumin Gene Expression in a Panel of Human Chromosome 2 Microcell Hybrids von Cerosaletti, Karen M., Fournier, R.E.K.

Volltext

Nijmegen breakage syndrome in a Dutch patient not resulting from a defect in NBS1 von Hiel, J A P, Weemaes, C M R, van Engelen, B G M, Smeets, D, Ligtenberg, M, van der Burgt, I, van den Heuvel, L P W J, Cerosaletti, K M, Gabreëls, F J M, Concannon, P

Volltext

Comparison of latex agglutination and counterimmunoelectrophoresis for the detection of pneumococcal antigen in elderly pneumonia patients von CEROSALETTI, K. M, ROGHMANN, M. C, BENTLEY, D. W

Volltext

Molecular analysis of deficient class I H-2 antigen expression by mouse lung carcinoma cells von Bahler, DW, Cerosaletti, KM, Lord, EM, Frelinger, JG

Volltext

Class‐I MHC expression in the mouse lung carcinoma, line 1: A model for class‐I inducible tumors von Blieden, Timothy M., McAdam, Alexander J., Foresman, Mark D., Cerosaletti, Karen M., Frelinger, John G., Lord, Edith M.

Volltext

Two regions of the H-2 Dd promoter are responsive to dimethylsulfoxide in line 1 cells by a mechanism distinct from IFN-gamma von Cerosaletti, KM, Woodward, JG, Lord, EM, Frelinger, JG

Volltext

Alteration of the metastatic potential of line 1 lung carcinoma cells: Opposite effects of class I antigen induction by interferons versus DMSO or gene transfection von Cerosaletti, Karen M., Blieden, Timothy M., Harwell, Lee W., Welsh, Kelly M., Frelinger, John G., Lord, Edith M.

Volltext

Nijmegen breakage syndrome: Clinical characteristics and mutation analysis in eight unrelated Russian families von Resnick, Igor B., Kondratenko, Irina, Togoev, Oleg, Vasserman, Natalia, Shagina, Irena, Evgrafov, Oleg, Tverskaya, Svetlana, Cerosaletti, Karen M., Gatti, Richard A., Concannon, Patrick

Volltext

Cloning mammary cell cDNAs from 17q12–q23 using interspecific somatic cell hybrids and subtractive hybridization von Cerosaletti, Karen M., Shapero, Michael H., Fournier, R.E.K.

Volltext