Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease
Clark, L N, Ross, B M, Wang, Y, Mejia-Santana, H, Harris, J, Louis, E D, Cote, L J, Andrews, H, Fahn, S, Waters, C, Ford, B, Frucht, S, Ottman, R, Marder, K
Published in Neurology (18.09.2007)
Published in Neurology (18.09.2007)
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Null Mutation of the Murine ATP7B (Wilson Disease) Gene Results in Intracellular Copper Accumulation and Late-Onset Hepatic Nodular Transformation
Buiakova, Olesia I., Xu, Jin, Lutsenko, Svetlana, Zeitlin, Scott, Das, Kamna, Das, Shonit, Ross, Barbara M., Mekios, Constantinos, Scheinberg, I. Herbert, Gilliam, T. Conrad
Published in Human molecular genetics (01.09.1999)
Published in Human molecular genetics (01.09.1999)
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Biomarkers of oxidative stress in schizophrenic and control subjects
Young, J, McKinney, S.B, Ross, B.M, Wahle, K.W.J, Boyle, S.P
Published in Prostaglandins, leukotrienes and essential fatty acids (01.02.2007)
Published in Prostaglandins, leukotrienes and essential fatty acids (01.02.2007)
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Transgenic mice expressing the human heat shock protein 70 have improved post-ischemic myocardial recovery
Plumier, Jean-Christophe, Ross, B, Currie, R. W, Angelidis, C. E, Kazlaris, H, Kollias, G, Pagoulatos, G. N
Published in The Journal of clinical investigation (01.04.1995)
Published in The Journal of clinical investigation (01.04.1995)
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ClpB is the Escherichia coli heat shock protein F84.1
SQUIRES, C. L, PEDERSEN, S, ROSS, B. M, SQUIRES, C
Published in Journal of Bacteriology (01.07.1991)
Published in Journal of Bacteriology (01.07.1991)
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Journal Article
Identification and Analysis of Mutations in the Wilson Disease Gene ( ATP7B): Population Frequencies, Genotype-Phenotype Correlation, and Functional Analyses
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
Published in American journal of human genetics (01.08.1997)
Published in American journal of human genetics (01.08.1997)
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Elevated activity of phospholipid biosynthetic enzymes in substantia nigra of patients with Parkinson's disease
Ross, B.M, Mamalias, N, Moszczynska, A, Rajput, A.H, Kish, S.J
Published in Neuroscience (01.01.2001)
Published in Neuroscience (01.01.2001)
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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
Petrukhin, K, Lutsenko, S, Chernov, I, Ross, B M, Kaplan, J H, Gilliam, T C
Published in Human molecular genetics (01.09.1994)
Published in Human molecular genetics (01.09.1994)
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TULP1 mutation in two extended Dominican kindreds with autosomal recessive Retinitis pigmentosa
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
Published in Nature genetics (01.02.1998)
Published in Nature genetics (01.02.1998)
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Laminar flow characterization using low-field magnetic resonance techniques
Ross, Michael M. B., Newling, Benedict, Lawrence, Maggie, Balcom, Bruce J.
Published in Physics of fluids (1994) (01.10.2021)
Published in Physics of fluids (1994) (01.10.2021)
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A Multicopy Transcription-Repair Gene, BTF2p44, Maps to the SMA Region and Demonstrates SMA Associated Deletions
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
Published in Human molecular genetics (01.02.1997)
Published in Human molecular genetics (01.02.1997)
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A portable, submersible, MR sensor – The Proteus magnet
Ross, Michael M.B., Wilbur, Grant R., Cano Barrita, Prisciliano F.de J., Balcom, Bruce J.
Published in Journal of magnetic resonance (1997) (01.05.2021)
Published in Journal of magnetic resonance (1997) (01.05.2021)
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Journal Article
Characterization of Survival Motor Neuron (SMNT) Gene Deletions in Asymptomatic Carriers of Spinal Muscular Atrophy
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.
Published in Human molecular genetics (01.03.1996)
Published in Human molecular genetics (01.03.1996)
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Cisplatin, Etoposide, and Paclitaxel in the Treatment of Patients With Extensive Small-Cell Lung Carcinoma
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
Published in Journal of clinical oncology (01.08.1999)
Published in Journal of clinical oncology (01.08.1999)
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Construction of a Yeast Artificial Chromosome Contig Spanning the Spinal Muscular Atrophy Disease Gene Region
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
Published in Proceedings of the National Academy of Sciences - PNAS (15.07.1993)
Published in Proceedings of the National Academy of Sciences - PNAS (15.07.1993)
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