Serum-Stable and Selective Backbone-N-Methylated Cyclic Peptides That Inhibit Prokaryotic Glycolytic Mutases von van Neer, R.H.P., Dranchak, P. K., Liu, L., Aitha, M., Queme, B., Kimura, H., Katoh, T., Battaile, K. P., Lovell, S., Inglese, J., Suga, H.

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In vivo selection of wild-type hematopoietic stem cells in a murine model of Fanconi anemia von BATTAILE, K. P, BATEMAN, R. L, MORTIMER, D, MULCAHY, J, RATHBUN, R. K, BAGBY, G, FLEMING, W. H, GROMPE, M

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Structures of isobutyryl-CoA dehydrogenase and enzyme-product complex: comparison with isovaleryl- and short-chain acyl-CoA dehydrogenases von Battaile, Kevin P, Nguyen, Tien V, Vockley, Jerry, Kim, Jung-Ja P

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Biochemical, phenotypic and neurophysiological characterization of a genetic mouse model of RSH/Smith-Lemli-Opitz syndrome von WASSLF, Christopher A, PINJUN ZHU, STEWART, Randall R, PORTER, Forbes D, KRATZ, Lisa, KRAKOWIAK, Patrycja A, BATTAILE, Kevin P, WEIGHT, Forrest F, GRINBERG, Alexander, STEINER, Robert D, NWOKORO, Ngozi A, KELLEY, Richard I

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Crystal structure of rat short chain acyl-CoA dehydrogenase complexed with acetoacetyl-CoA: comparison with other acyl-CoA dehydrogenases von Battaile, Kevin P, Molin-Case, JoAnn, Paschke, Rosemary, Wang, Ming, Bennett, Dennis, Vockley, Jerry, Kim, Jung-Ja P

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Smith-Lemli-Opitz Syndrome: The First Malformation Syndrome Associated with Defective Cholesterol Synthesis von Battaile, Kevin P., Steiner, Robert D.

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Lowered DHCR7 activity measured by ergosterol conversion in multiple cell types in Smith–Lemli–Opitz syndrome von Ginat, Sharon, Battaile, Kevin P., Battaile, Brian C., Maslen, Cheryl, Gibson, K. Michael, Steiner, Robert D.

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Ab Initio Structural Modeling of and Experimental Validation for Chlamydia trachomatis Protein CT296 Reveal Structural Similarity to Fe(II) 2-Oxoglutarate-Dependent Enzymes von Kemege, Kyle E, Hickey, John M, Lovell, Scott, Battaile, Kevin P, Zhang, Yang, Hefty, P. Scott

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Towards protein-crystal centering using second-harmonic generation (SHG) microscopy von Kissick, David J., Dettmar, Christopher M., Becker, Michael, Mulichak, Anne M., Cherezov, Vadim, Ginell, Stephan L., Battaile, Kevin P., Keefe, Lisa J., Fischetti, Robert F., Simpson, Garth J.

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Characterization of Molecular Defects in Isovaleryl-CoA Dehydrogenase in Patients with Isovaleric Acidemia von Mohsen, Al-Walid A, Anderson, Bambi D, Volchenboum, Samuel L, Battaile, Kevin P, Tiffany, Karen, Roberts, David, Kim, Jung-Ja P, Vockley, Jerry

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Fetal demise with Smith-Lemli-Opitz syndrome confirmed by tissue sterol analysis and the absence of measurable 7-dehydrocholesterol Delta(7)-reductase activity in chorionic villi von Linck, L M, Hayflick, S J, Lin, D S, Battaile, K P, Ginat, S, Burlingame, T, Gibson, K M, Honda, M, Honda, A, Salen, G, Tint, G S, Connor, W E, Steiner, R D

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Functional Role of the Active Site Glutamate-368 in Rat Short Chain Acyl-CoA Dehydrogenase von Battaile, Kevin P, Mohsen, Al-Walid A, Vockley, Jerry

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Carrier Frequency of the Common Mutation IVS8-1G>C in DHCR7 and Estimate of the Expected Incidence of Smith–Lemli–Opitz Syndrome von Battaile, Kevin P., Battaile, Brian C., Merkens, Louise S., Maslen, Cheryl L., Steiner, Robert D.

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Cloning of a cDNA for Short/Branched Chain Acyl-Coenzyme A Dehydrogenase from Rat and Characterization of Its Tissue Expression and Substrate Specificity von Willard, Jan, Vicanek, Caroline, Battaile, Kevin P., Van Veldhoven, Paul P., Fauq, Abdul H., Rozen, Rima, Vockley, Jerry

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Burning fat: the structural basis of fatty acid β-oxidation von Kim, Jung-Ja P, Battaile, Kevin P

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Redesigning the active-site of an acyl-CoA dehydrogenase: new evidence supporting a one-base mechanism von Dakoji, Srikanth, Shin, Injae, Battaile, Kevin P., Vockley, Jerry, Liu, Hung-wen

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Fetal demise with Smith-Lemli-Opitz syndrome confirmed by tissue sterol analysis and the absence of measurable 7-dehydrocholesterol Δ7-reductase activity in chorionic villi von Linck, L. M., Hayflick, S. J., Lin, D. S., Battaile, K. P., Ginat, S., Burlingame, T., Gibson, K. M., Honda, M., Honda, A., Salen, G., Tint, G. S., Connor, W. E., Steiner, R. D.

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Fanconi anemia group A and C double-mutant mice: Functional evidence for a multi-protein Fanconi anemia complex von Noll, Meenakshi, Battaile, Kevin P, Bateman, Raynard, Lax, Timothy P, Rathbun, Keany, Reifsteck, Carol, Bagby, Grover, Finegold, Milton, Olson, Susan, Grompe, Markus

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A simple PCR-based assay allows detection of a common mutation, IVS8-1G-->C, in DHCR7 in Smith-Lemli-Opitz syndrome von Battaile, K P, Maslen, C L, Wassif, C A, Krakowiak, P, Porter, F D, Steiner, R D

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Fetal demise with Smith-Lemli-Opitz syndrome confirmed by tissue sterol analysis and the absence of measurable 7-dehydrocholesterol ?7-reductase activity in chorionic villi von Linck, L. M., Hayflick, S. J., Lin, D. S., Battaile, K. P., Ginat, S., Burlingame, T., Gibson, K. M., Honda, M., Honda, A., Salen, G., Tint, G. S., Connor, W. E., Steiner, R. D.

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