Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease von CLARK, L. N, ROSS, B. M, FORD, B, FRUCHT, S, OTTMAN, R, MARDER, K, WANG, Y, MEJIA-SANTANA, H, HARRIS, J, LOUIS, E. D, COTE, L. J, ANDREWS, H, FAHN, S, WATERS, C

Volltext

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

Volltext

Biomarkers of oxidative stress in schizophrenic and control subjects von Young, J, McKinney, S.B, Ross, B.M, Wahle, K.W.J, Boyle, S.P

Volltext

Transgenic mice expressing the human heat shock protein 70 have improved post-ischemic myocardial recovery von Plumier, Jean-Christophe, Ross, B, Currie, R. W, Angelidis, C. E, Kazlaris, H, Kollias, G, Pagoulatos, G. N

Volltext

The analysis of oral air using selected ion flow tube mass spectrometry in persons with and without a history of oral malodour von Ross, BM, Dadgostar, N, Bloom, M, McKeown, L

Volltext

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

Volltext

Laminar flow characterization using low-field magnetic resonance techniques von Ross, Michael M. B., Newling, Benedict, Lawrence, Maggie, Balcom, Bruce J.

Volltext

ClpB is the Escherichia coli heat shock protein F84.1 von SQUIRES, C. L, PEDERSEN, S, ROSS, B. M, SQUIRES, C

Volltext

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

Volltext

A portable, submersible, MR sensor – The Proteus magnet von Ross, Michael M.B., Wilbur, Grant R., Cano Barrita, Prisciliano F.de J., Balcom, Bruce J.

Volltext

Elevated activity of phospholipid biosynthetic enzymes in substantia nigra of patients with Parkinson's disease von Ross, B.M, Mamalias, N, Moszczynska, A, Rajput, A.H, Kish, S.J

Volltext

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

Volltext

Low activity of key phospholipid catabolic and anabolic enzymes in human substantia nigra: possible implications for Parkinson's disease von Ross, B.M, Moszczynska, A, Erlich, J, Kish, S.J

Volltext

Application packs von Ross, M B

Volltext

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

Volltext

Cisplatin, Etoposide, and Paclitaxel in the Treatment of Patients With Extensive Small-Cell Lung Carcinoma von GLISSON, B. S, KURIE, J. M, SHIN, D. M, WAUN KI HONG, PEREZ-SOLER, R, FOX, N. J, MURPHY, W. K, FOSSELLA, F. V, LEE, J. S, ROSS, M. B, NYBERG, D. A, PISTERS, K. M. W

Volltext

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.

Volltext

Differential alteration of phospholipase A2 activities in brain of patients with schizophrenia von ROSS, B. M, TURENNE, S, MOSZCZYNSKA, A, WARSH, J. J, KISH, S. J

Volltext

Phospholipid‐Metabolizing Enzymes in Alzheimer's Disease: Increased Lysophospholipid Acyltransferase Activity and Decreased Phospholipase A2 Activity von Ross, Brian M., Moszczynska, Anna, Erlich, Jeffrey, Kish, Stephen J.

Volltext

Construction of a Yeast Artificial Chromosome Contig Spanning the Spinal Muscular Atrophy Disease Gene Region von Kleyn, Patrick W., Wang, Ching H., Lien, Lyndon L., Vitale, Emilia, Pan, Jie, Ross, Barbara M., Grunn, Adina, Palmer, David A., Warburton, Dorothy, Brzustowicz, Linda M., Kunkel, Louis M., Gilliam, T. Conrad

Volltext