Carrier localization in the vicinity of dislocations in InGaN von Massabuau, F. C-P., Chen, P., Horton, M. K., Rhode, S. L., Ren, C. X., O'Hanlon, T. J., Kovács, A., Kappers, M. J., Humphreys, C. J., Dunin-Borkowski, R. E., Oliver, R. A.

Volltext

Dislocations at coalescence boundaries in heteroepitaxial GaN/sapphire studied after the epitaxial layer has completely coalesced von O'Hanlon, T.J., Zhu, T., Massabuau, F.C.-P., Oliver, R.A.

Volltext

Directly correlated microscopy of trench defects in InGaN quantum wells von O'Hanlon, T.J., Massabuau, F C-P., Bao, A., Kappers, M.J., Oliver, R.A.

Volltext

Cross-shaped markers for the preparation of site-specific transmission electron microscopy lamellae using focused ion beam techniques von O'Hanlon, T.J., Bao, A., Massabuau, F.C.-P., Kappers, M.J., Oliver, R.A.

Volltext

γδ T cell receptor gene expression by muscle‐infiltrating lymphocytes in the idiopathic inflammatory myopathies von O'HANLON, T. P., MESSERSMITH, W. A., DALAKAS, M. C., PLOTZ, P. H., MILLER, F. W.

Volltext

Broadband Quantum Enhancement of the LIGO Detectors with Frequency-Dependent Squeezing von Ganapathy, D., Jia, W., Nakano, M., Xu, V., Aritomi, N., Cullen, T., Kijbunchoo, N., Dwyer, S. E., Mullavey, A., McCuller, L., Abbott, R., Abouelfettouh, I., Adhikari, R. X., Ananyeva, A., Appert, S., Arai, K., Aston, S. M., Ball, M., Ballmer, S. W., Barker, D., Barsotti, L., Berger, B. K., Betzwieser, J., Bhattacharjee, D., Billingsley, G., Biscans, S., Bode, N., Bonilla, E., Bossilkov, V., Branch, A., Brooks, A. F., Brown, D. D., Bryant, J., Cahillane, C., Cao, H., Capote, E., Clara, F., Collins, J., Compton, C. M., Cottingham, R., Coyne, D. C., Crouch, R., Csizmazia, J., Dartez, L. P., Demos, N., Dohmen, E., Driggers, J. C., Effler, A., Ejlli, A., Etzel, T., Evans, M., Feicht, J., Frey, R., Frischhertz, W., Fritschel, P., Frolov, V. V., Fulda, P., Fyffe, M., Gateley, B., Giaime, J. A., Giardina, K. D., Glanzer, J., Goetz, E., Goetz, R., Goodwin-Jones, A. W., Gras, S., Gray, C., Griffith, D., Grote, H., Guidry, T., Hall, E. D., Hanks, J., Hanson, J., Heintze, M. C., Helmling-Cornell, A. F., Holland, N. A., Hoyland, D., Huang, H. Y., Inoue, Y., James, A. L., Jennings, A., Karat, S., Karki, S., Kasprzack, M., Kawabe, K., King, P. J., Kissel, J. S., Komori, K., Kontos, A., Kumar, R., Kuns, K., Landry, M., Lantz, B., Laxen, M., Lee, K., Lesovsky, M., Llamas, F., Lormand, M., Loughlin, H. A., Macas, R.

Volltext

Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes von Miller, F W, Chen, W, O'Hanlon, T P, Cooper, R G, Vencovsky, J, Rider, L G, Danko, K, Wedderburn, L R, Lundberg, I E, Pachman, L M, Reed, A M, Ytterberg, S R, Padyukov, L, Selva-O'Callaghan, A, Radstake, T R, Isenberg, D A, Chinoy, H, Ollier, W E R, Scheet, P, Peng, B, Lee, A, Byun, J, Lamb, J A, Gregersen, P K, Amos, C I

Volltext

Age-related accumulation of somatic structural changes in the nuclear genome of human blood cells in vivo von Dumanski, Jan P., Forsberg, L. A., Rasi, C., Razzaghian, H. R., Pakalapati, G., Waite, L., Thilbeault, K. Stanton, Ronowicz, A., Wineinger, N. E., Tiwari, H. K., Boomsma, D., Westerman, M. P., Harris, J. R., Lyle, R., Essand, M., Eriksson, F., Assimes, T. L., Iribarren, C., Strachan, E., O'Hanlon, T. P., Rider, L. G., Miller, F. W., Giedraitis, Vilmantas, Lannfelt, Lars, Ingelsson, Martin, Piotrowski, A., Pedersen, N. L., Absher, D.

Volltext

Complement C4 gene copy number variations and polymorphisms, autoantibodies, and clinical manifestations of juvenile dermatomyositis– a multi-center study von Coss, Samantha Lynn, Aziz, Rabheh Abdul, Zhou, Danlei, Zhou, Bi, Miller, Katherine, Wu, Yee Ling, Ardoin, Stacy, Oberle, Edward, Driest, Kyla, Al Ahmed, Ohoud, Patwardhan, Anjali, Akoghlanian, Shoghik, Sivaraman, Vidya, Barbar-Smiley, Fatima, Drew, Joanne, Spencer, Charles, Pachman, Lauren, Morgan, Gabrielle, Mamyrova, Gulnara, Curiel, Rodolfo, Jones, Olcay, O’Hanlon, Terry, Rider, Lisa, Miller, Frederick, Padyukov, Leonid, Lundberg, Ingrid, Notarnicola, Antonella, Vencovský, Jiří, Stibůrková, Blanka, Kryštůfková, Olga, Yu, Chack-Yung

Volltext

PIK3Cδ expression by fibroblasts promotes triple-negative breast cancer progression von Gagliano, T, Shah, K, Gargani, S, Lao, L, Alsaleem, M, Chen, J, Ntafis, V, Huang, P, Ditsiou, A, Vella, V, Yadav, K, Bienkowska, K, Bresciani, G, Kang, K, Li, L, Carter, P, Benstead-Hume, G, O'Hanlon, T, Dean, M, Pearl, FM, Lee, SC, Rakha, EA, Green, AR, Kontoyiannis, DL, Song, E, Stebbing, J, Giamas, G

Volltext

Genomic organization, transcriptional mapping, and evolutionary implications of the human bi-directional histidyl-tRNA synthetase locus (HARS/HARSL) von O'Hanlon, Terrance P., Miller, Frederick W.

Volltext

LMTK3 confers chemo-resistance in breast cancer von Stebbing, J, Shah, K, Lit, LC, Gagliano, T, Ditsiou, A, Wang, T, Wendler, F, Simon, T, Szabó, KS, O'Hanlon, T, Dean, M, Roslani, AC, Cheah, SH, Lee, S-C, Giamas, G

Volltext

Gene expression profiles from discordant monozygotic twins suggest that molecular pathways are shared among multiple systemic autoimmune diseases von O'Hanlon, Terrance P, Rider, Lisa G, Gan, Lu, Fannin, Rick, Paules, Richard S, Umbach, David M, Weinberg, Clarice R, Shah, Ruchir R, Mav, Deepak, Gourley, Mark F, Miller, Frederick W

Volltext

Low Gene Copy Numbers (GCN) of complement C4 and C4A deficiency are highly significant genetic risk factors for idiopathic inflammatory myopathies and its major subgroups von Zhou, D, King, E, Rothwell, S, Krystufkova, O, Notarnicola, A, Coss, S, Aziz, R, Miller, K, Dang, A, Yu, R, Drew, J, Lundstrom, E, Pachman, L, Mamyrova, G, Curiel, R, De Paepe, B, De Bleecker, J, Payton, A, Ollier, W, O'Hanlon, T, Targoff, I, Flegel, W, Sivaraman, V, Obele, E, Akoghlanian, S, Driest, K, Spencer, C, Wu, YL, Nagaraja, H, Ardoin, S, Chinoy, H, Rider, L, Miller, F, Lundberg, I, Padyukov, L, Vencovsky, J, Lamb, J, Yu, CY

Volltext

Regulation of β-Galactoside α 2,6-Sialyltransferase Gene Expression by Dexamethasone von Wang, X C, O'Hanlon, T P, Lau, J T Y

Volltext

Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis von Lintner, Katherine E, Patwardhan, Anjali, Rider, Lisa G, Abdul-Aziz, Rabheh, Wu, Yee Ling, Lundström, Emeli, Padyukov, Leonid, Zhou, Bi, Alhomosh, Alaaedin, Newsom, David, White, Peter, Jones, Karla B, O'Hanlon, Terrance P, Miller, Frederick W, Spencer, Charles H, Yu, Chack Yung

Volltext

Trial of Decompressive Craniectomy for Traumatic Intracranial Hypertension von Hutchinson, Peter J, Kolias, Angelos G, Timofeev, Ivan S, Corteen, Elizabeth A, Czosnyka, Marek, Timothy, Jake, Anderson, Ian, Bulters, Diederik O, Belli, Antonio, Eynon, C. Andrew, Wadley, John, Mendelow, A. David, Mitchell, Patrick M, Wilson, Mark H, Critchley, Giles, Sahuquillo, Juan, Unterberg, Andreas, Servadei, Franco, Teasdale, Graham M, Pickard, John D, Menon, David K, Murray, Gordon D, Kirkpatrick, Peter J

Volltext

T cell-mediated immune mechanisms in myositis von OʼHanlon, Terrance P, Miller, Frederick W

Volltext

Genome-wide meta-analysis reveals shared new loci in systemic seropositive rheumatic diseases von Acosta-Herrera, M, Kerick, M, Gonzalez-Serna, D, Wijmenga, C, Franke, A, Gregersen, PK, Padyukov, L, Worthington, J, Vyse, TJ, Alarcon-Riquelme, ME, Mayes, MD, Martin, J, Miller, FW, Chen, W, O'Hanlon, TP, Cooper, RG, Vencovsky, J, Rider, LG, Danko, K, Wedderburn, LR, Lundberg, IE, Pachman, LM, Reed, AM, Ytterberg, SR, Selva-O'Callaghan, A, Radstake, TR, Isenberg, DA, Chinoy, H, Ollier, WER, Scheet, P, Peng, B, Lee, A, Lamb, JA, Amos, CI, Denton, C, Hilton-Jones, D, Plotz, PH, Varsani, H, Radstake, TRDJ, Gorlova, O, Rueda, B, Martin, JE, Alizadeh, BZ, Palomino-Morales, R, Coenen, MJ, Vonk, MC, Voskuyl, AE, Scheurwegh, AJ, Broen, JC, van Riel, PLCM, van 't Slot, R, Italiaander, A, Ophoff, RA, Riemekasten, G, Hunzelmann, N, Simeon, CP, Ortego-Centeno, N, Gonzalez-Gay, MA, Gonzalez-Escribano, MF, Airo, P, van Laar, J, Herrick, A, Hesselstrand, R, Smith, V, de Keyser, F, Houssiau, F, Chee, MM, Madhok, R, Shiels, P, Westhovens, R, Kreuter, A, Kiener, H, de Baere, E, Witte, T, Klareskog, L, Beretta, L, Scorza, R, Lie, BA, Hoffman-Vold, AM, Carreira, P, Varga, J, Hinchcliff, M, Lee, AT, Ying, J, Han, Y, Weng, SF, Wigley, FM, Hummers, L, Nelson, JL, Agarwal, SK, Assassi, S, Gourh, P, Tan, FK, Koeleman, BPC, Arnett, FC

Volltext

Human Leukocyte Antigen Alleles Associated with Interstitial Lung Disease in North Americans with Idiopathic Inflammatory Myopathy von Johnson, Cheilonda, Schiffenbauer, Adam I, Miller, Frederick W, Perin, Jamie, Danoff, Sonye K, Diwadkar, Avantika R, Joo, Jaehyun, Himes, Blanca E, Meyer, Nuala J

Volltext