RNA-Binding Site in T7 RNA Polymerase von Sastry, Srin, Ross, Barbara M.

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Null Mutation of the Murine ATP7B (Wilson Disease) Gene Results in Intracellular Copper Accumulation and Late-Onset Hepatic Nodular Transformation von Buiakova, Olesia I., Xu, Jin, Lutsenko, Svetlana, Zeitlin, Scott, Das, Kamna, Das, Shonit, Ross, Barbara M., Mekios, Constantinos, Scheinberg, I. Herbert, Gilliam, T. Conrad

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Association between lipoprotein lipase (LPL) gene and blood lipids: A common variant for a common trait? von Morabia, Alfredo, Cayanis, Eftihia, Costanza, Michael C., Ross, Barbara M., Bernstein, Martine S., Flaherty, Maria Sol, Alvin, Gabriela B., Das, Kamna, Morris, Michael A., Penchaszadeh, Graciela K., Zhang, Peizen, Gilliam, T. Conrad

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Neuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD Study von Caccappolo, Elise, Alcalay, Roy N., Mejia-Santana, Helen, Tang, Ming-X., Rakitin, Brian, Rosado, Llency, Louis, Elan D., Comella, Cynthia L., Colcher, Amy, Jennings, Danna, Nance, Martha A., Bressman, Susan, Scott, William K., Tanner, Caroline M., Mickel, Susan F., Andrews, Howard F., Waters, Cheryl, Fahn, Stanley, Cote, Lucien J., Frucht, Steven, Ford, Blair, Rezak, Michael, Novak, Kevin, Friedman, Joseph H., Pfeiffer, Ronald F., Marsh, Laura, Hiner, Brad, Siderowf, Andrew D., Ross, Barbara M., Verbitsky, Miguel, Kisselev, Sergey, Ottman, Ruth, Clark, Lorraine N., Marder, Karen S.

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Population-based study of SR-BI genetic variation and lipid profile von Morabia, Alfredo, Ross, Barbara M, Costanza, Michael C, Cayanis, Eftihia, Flaherty, Maria Sol, Alvin, Gabriela B, Das, Kamna, James, Richard, Yang, An-Suei, Evagrafov, Oleg, Gilliam, T.Conrad

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Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions von Petrukhin, Konstantin, Lutsenko, Svetiana, Chernov, Igor, Ross, Barbara M., Kaplan, Jack H., Gilliam, T.Conrad

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Relative Contributions of Genes, Environment, and Interactions to Blood Lipid Concentrations in a General Adult Population von Costanza, Michael C., Cayanis, Eftihia, Ross, Barbara M., Flaherty, Maria Sol, Alvin, Gabriela B., Das, Kamna, Morabia, Alfredo

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TULP1 mutation in two extended Dominican kindreds with autosomal recessive Retinitis pigmentosa von Banerjee, Poulabi, Kleyn, Patrick W, Knowles, James A, Lewis, Charles A, Ross, Barbara M, Parano, Enrico, Kovats, Steve G, Lee, John J, Penchaszadeh, Graciela K, Ott, Jürg, Jacobson, Samuel G, Gilliam, T. Conrad

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Association of extreme blood lipid profile phenotypic variation with 11 reverse cholesterol transport genes and 10 non-genetic cardiovascular disease risk factors von Morabia, Alfredo, Cayanis, Eftihia, Costanza, Michael C., Ross, Barbara M., Flaherty, Maria Sol, Alvin, Gabriela B., Das, Kamna, Gilliam, T. Conrad

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Probing the Interaction of T7 RNA Polymerase with Promoter von Sastry, Srin, Ross, Barbara M

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Nuclease Activity of T7 RNA Polymerase and the Heterogeneity of Transcription Elongation Complexes von Sastry, Srinivas S., Ross, Barbara M.

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A Direct Real-Time Spectroscopic Investigation of the Mechanism of Open Complex Formation by T7 RNA Polymerase von Sastry, Srinivas S, Ross, Barbara M

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Mechanisms for the Processing of a Frozen Topoisomerase-DNA Conjugate by Human Cell-free Extracts von Sastry, S, Ross, B M

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Probing the Mechanisms of T7 RNA Polymerase Transcription Initiation Using Photochemical Conjugation of Psoralen to a Promoter von Sastry, Srinivas S, Ross, Barbara M

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Cross-linking of DNA-binding Proteins to DNA with Psoralen and Psoralen Furan-side Monoadducts von Sastry, Srinivas S., Ross, Barbara M., P'arraga, Antonio

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Identification and Analysis of Mutations in the Wilson Disease Gene ( ATP7B): Population Frequencies, Genotype-Phenotype Correlation, and Functional Analyses von Shah, Anjali B., Chernov, Igor, Zhang, Hong Tao, Ross, Barbara M., Das, Kamna, Lutsenko, Svetlana, Parano, Enrico, Pavone, Lorenzo, Evgrafov, Oleg, Ivanova-Smolenskaya, Irina A., Annerén, Göran, Westermark, Kerstin, Urrutia, Francisco Hevia, Penchaszadeh, Graciela K., Sternlieb, Irmin, Scheinberg, I. Herbert, Gilliam, T. Conrad, Petrukhin, Konstantin

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Characterization of Survival Motor Neuron (SMNT) Gene Deletions in Asymptomatic Carriers of Spinal Muscular Atrophy von Wang, Ching H., Xu, Jin, Carter, Todd A., Ross, Barbara M., Dominski, Mary K., Bellcross, Cecelia A., Penchaszadeh, Graciela K., Munsat, Theodore L., Conrad Gilliam, T.

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A Multicopy Transcription-Repair Gene, BTF2p44, Maps to the SMA Region and Demonstrates SMA Associated Deletions von Carter, Todd A., Bönnemann, Carsten G., Wang, Ching H., Obici, Silvana, Parano, Enrico, De Fatima Bonaldo, Maria, Ross, Barbara M., Penchaszadeh, Graciela K., Mackenzie, Alex, Soares, Marcelo Bento, Kunkel, Louis M., Gilliam, T. Conrad

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Utilizing a Floor Decal to Improve Hand Hygiene After Caring for Patients with Clostridium difficile Infection von Albert, Kathryn, RN, BSN, CIC, Calfee, David, MD, MS, Mangino, Diane, MSN, RN, CIC, D'Agostino, John, RN, MSN, CIC, Mendez-Augsburg, Grimilda, Furuya, E. Yoko, MD MS, Ross, Barbara, RN, MS, CIC, FAPIC

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Electronic surveillance for catheter-associated urinary tract infections at a university-affiliated children's hospital von Sen, Anita I., MD, Balzer, Krystal, RN, MSN, Mangino, Diane, RN, MSN, Messina, Maria, RN, BS, Ross, Barbara, RN, MS, Zachariah, Philip, MD, MS, Saiman, Lisa, MD, MPH

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