Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome von Collins, Francis S, Eriksson, Maria, Brown, W. Ted, Gordon, Leslie B, Glynn, Michael W, Singer, Joel, Scott, Laura, Erdos, Michael R, Robbins, Christiane M, Moses, Tracy Y, Berglund, Peter, Dutra, Amalia, Pak, Evgenia, Durkin, Sandra, Csoka, Antonei B, Boehnke, Michael, Glover, Thomas W

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BRCA1 Inhibition of Estrogen Receptor Signaling in Transfected Cells von Fan, S., J.-A. Wang, Yuan, R., Ma, Y., Meng, Q., Erdos, M. R., Pestell, R. G., Yuan, Fang, Auborn, K. J., Goldberg, I. D., Rosen, E. M.

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Accumulation of Mutant Lamin A Causes Progressive Changes in Nuclear Architecture in Hutchinson-Gilford Progeria Syndrome von Goldman, Robert D., Shumaker, Dale K., Erdos, Michael R., Eriksson, Maria, Goldman, Anne E., Gordon, Leslie B., Gruenbaum, Yosef, Khuon, Satya, Mendez, Melissa, Varga, Renée, Collins, Francis S.

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Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer von Castilla, Lucio H, Couch, Fergus J, Erdos, Michael R, Hoskins, Kent F, Calzone, Kathy, Garber, Judy E, Boyd, Jeff, Lubin, Matthew B, Deshano, Michelle L, Brody, Lawrence C, Collins, Francis S, Weber, Barbara L

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BRCA1 as a potential human prostate tumor suppressor : modulation of proliferation, damage responses and expression of cell regulatory proteins von SAIJUN FAN, WANG, J.-A, YUAN, R.-Q, YONG XIAN MA, QINGHUI MENG, ERDOS, M. R, BRODY, L. C, GOLDBERG, I. D, ROSEN, E. M

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Evolutionary sequence comparisons using high-density oligonucleotide arrays von Hacia, Joseph G, Makalowski, Wojciech, Edgemon, Keith, Erdos, Michael R, Robbins, Christiane M, Fodor, Stephen P. A, Brody, Lawrence C, Collins, Francis S

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Menin Interacts with the AP1 Transcription Factor JunD and Represses JunD-Activated Transcription von Agarwal, Sunita K., Guru, Siradanahalli C., Heppner, Christina, Erdos, Michael R., Collins, Regina M., Park, Sylvia Y., Saggar, Suraj, Chandrasekharappa, Settara C., Collins, Francis S., Spiegel, Allen M., Marx, Stephen J., Burns, A.Lee

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Correlated alterations in genome organization, histone methylation, and DNA-lamin A/C interactions in Hutchinson-Gilford progeria syndrome von McCord, Rachel Patton, Nazario-Toole, Ashley, Zhang, Haoyue, Chines, Peter S, Zhan, Ye, Erdos, Michael R, Collins, Francis S, Dekker, Job, Cao, Kan

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Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in Finns von MOHLKE, Karen L, JACKSON, Anne U, NARISU, Narisu, ENLOE, Sareena, VALLE, Timo T, TUOMILEHTO, Jaakko, BERGMAN, Richard N, BOEHNKE, Michael, COLLINS, Francis S, SCOTT, Laura J, PECK, Erin C, SUH, Yong D, CHINES, Peter S, WATANABE, Richard M, BUCHANAN, Thomas A, CONNEELY, Karen N, ERDOS, Michael R

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High-Throughput Screening for Evidence of Association by Using Mass Spectrometry Genotyping on DNA Pools von Mohlke, Karen L., Erdos, Michael R., Scott, Laura J., Fingerlin, Tasha E., Jackson, Anne U., Silander, Kaisa, Hollstein, Pablo, Boehnke, Michael, Collins, Francis S.

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Type 2 Diabetes: Evidence for Linkage on Chromosome 20 in 716 Finnish Affected Sib Pairs von Ghosh, Soumitra, Watanabe, Richard M., Hauser, Elizabeth R., Valle, Timo, Magnuson, Victoria L., Erdos, Michael R., Langefeld, Carl D., Balow, James, Ally, Delphine S., Kohtamaki, Kimmo, Chines, Peter, Birznieks, Gunther, Kaleta, Hong-Shi, Musick, Anjene, Te, Catherine, Tannenbaum, Joyce, Eldridge, William, Shapiro, Shane, Martin, Colin, Witt, Alyson, So, Alistair, Chang, Jennie, Shurtleff, Ben, Porter, Rachel, Kudelko, Kristina, Unni, Arun, Segal, Leonid, Sharaf, Ravi, Blaschak-Harvan, Jillian, Eriksson, Johan, Tenkula, Tuula, Vidgren, Gabriele, Ehnholm, Christian, Tuomilehto-Wolf, Eva, Hagopian, William, Buchanan, Thomas A., Tuomilehto, Jaakko, Bergman, Richard N., Collins, Francis S., Boehnke, Michael

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Cellular Levels of Thymosin Immunoreactive Peptides are Linked to Proliferative Events: Evidence for a Nuclear Site of Action von Conteas, C. N., Mutchnick, M. G., Palmer, K. C., Weller, F. E., Luk, G. D., Naylor, P. H., Erdos, M. E., Goldstein, A. L., Panneerselvam, C., Horecker, B. L.

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Mutant Nuclear Lamin a Leads to Progressive Alterations of Epigenetic Control in Premature Aging von Shumaker, Dale K., Dechat, Thomas, Kohlmaier, Alexander, Adam, Stephen A., Bozovsky, Matthew R., Erdos, Michael R., Eriksson, Maria, Goldman, Anne E., Khuon, Satya, Collins, Francis S., Jenuwein, Thomas, Goldman, Robert D.

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Global genome splicing analysis reveals an increased number of alternatively spliced genes with aging von Rodríguez, Sofía A., Grochová, Diana, McKenna, Tomás, Borate, Bhavesh, Trivedi, Niraj S., Erdos, Michael R., Eriksson, Maria

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Characterization of EZH1, a human homolog of Drosophila enhancer of zeste near BRCA1 von ABEL, K. J, BRODY, L. C, LYNCH, E. D, KING, M.-C, WELCSH, P. L, OSBORNE-LAWRENCE, S, SPILLMAN, M, BOWCOCK, A. M, COLLINS, F. S, WEBER, B. L, VALDES, J. M, ERDOS, M. R, MCKINLEY, D. R, CASTILLA, L. H, MERAJVER, S. D, COUCH, F. J, FRIEDMAN, L. S, OSTERMEYER, E. A

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Human BRCA1 Inhibits Growth in Yeast: Potential use in Diagnostic Testing von Humphrey, Jeffrey S., Salim, Ali, Erdos, Michael R., Collins, Francis S., Brody, Lawrence C., Klausner, Richard D.

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BRCA1 Suppresses Insulin-like Growth Factor-I Receptor Promoter Activity: Potential Interaction between BRCA1 and Sp1 von Maor, Sharon B., Abramovitch, Shirley, Erdos, Mike R., Brody, Lawrence C., Werner, Haim

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Inhibiting Farnesylation of Progerin Prevents the Characteristic Nuclear Blebbing of Hutchinson-Gilford Progeria Syndrome von Capell, Brian C., Erdos, Michael R., Madigan, James P., Fiordalisi, James J., Varga, Renee, Conneely, Karen N., Gordon, Leslie B., Der, Channing J., Cox, Adrienne D., Collins, Francis S.

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Progressive Vascular Smooth Muscle Cell Defects in a Mouse Model of Hutchinson-Gilford Progeria Syndrome von Varga, Renee, Eriksson, Maria, Erdos, Michael R., Olive, Michelle, Harten, Ingrid, Kolodgie, Frank, Capell, Brian C., Cheng, Jun, Faddah, Dina, Perkins, Stacie, Avallone, Hedwig, San, Hong, Qu, Xuan, Ganesh, Santhi, Gordon, Leslie B., Virmani, Renu, Wight, Thomas N., Nabel, Elizabeth G., Collins, Francis S.

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Analysis of somatic mutations identifies signs of selection during in vitro aging of primary dermal fibroblasts von Narisu, Narisu, Rothwell, Rebecca, Vrtačnik, Peter, Rodríguez, Sofía, Didion, John, Zöllner, Sebastian, Erdos, Michael R., Collins, Francis S., Eriksson, Maria

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