A modified phenomenological description of the exchange interactions in dilute magnetic semiconductors von Nicholas, R J, Lawless, M J, Cheng, H H, Ashenford, D E, Lunn, B

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Valence band spin of semiconductor superlattices von Warburton, R.J., Lawless, M.J., Nicholas, R.J.

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Saddle-point excitons and intraband (Γ-II) mixing in strained-layer superlattices von LAWLESS, M. J, WARBURTON, R. J, NICHOLAS, R. J, PULSFORD, N. J, MOORE, K. J, DUGGAN, G, WOODBRIDGE, K

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Magneto-optical studies of the type-I/type-II crossover and band offset in ZnTe/Zn1-xMnxTe superlattices in magnetic fields up to 45 T von Cheng, HH, Nicholas, RJ, Lawless, MJ, Ashenford, DE, Lunn, B

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Strain and minibands in InGaAsGaAs superlattices von Pulsford, N.J., Nicholas, R.J., Warburton, R.J., Lawless, M.J., Duggan, G., Moore, K.J., Woodbridge, K., Roberts, C.

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Spectroscopic studies of miniband structure and band mixing in superlattices von Pulsford, N.J., Lawless, M.J., Nicholas, R.J., Duggan, G., Moore, K.J., Roberts, C., Woodbridge, K.

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Interband magneto-optical studies of resonant polaron coupling in CdTe/Cd1-xMnxTe quantum wells von Nicholas, RJ, Sasaki, S, Miura, N, Peeters, FM, Shi, JM, Hai, GQ, Devreese, JT, Lawless, MJ, Ashenford, DE, Lunn, B

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Recovery in Serious Mental Illness: A New Wine or Just a New Bottle? von Davidson, Larry, O'Connell, Maria J, Tondora, Janis, Lawless, Martha, Evans, Arthur C

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Discrete and Polymeric Self-Assembled Dendrimers: Hydrogen Bond-Mediated Assembly with High Stability and High Fidelity von Corbin, Perry S., Lawless, Laurence J., Li, Zhanting, Ma, Yuguo, Witmer, Melissa J., Zimmerman, Steven C.

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Stat4 regulates multiple components of IFN-gamma-inducing signaling pathways von Lawless, V A, Zhang, S, Ozes, O N, Bruns, H A, Oldham, I, Hoey, T, Grusby, M J, Kaplan, M H

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Use of Cryopreserved Cells for Enabling Greater Flexibility in Compound Profiling von Wigglesworth, M.J., Lawless, K.J., Standing, D.J., MacKenzie, E.K., Kitchen, V.R., McKay, F., Ward, E., Brough, S.J., Stylianou, M., Jewitt, F.R., McLaren-Douglas, A.M., Jowet, M.I., Tamayama, N., Finnigan, D., Ding, J., Wise, A.

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Failure inference from a marker process based on a bivariate Wiener model von Whitmore, G A, Crowder, M J, Lawless, J F

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Characterization of tumour necrosis factor-alpha genetic variants and mRNA expression in patients with severe sepsis von O'Dwyer, M. J., Mankan, A. K., Ryan, A. W., Lawless, M. W., Stordeur, P., Kelleher, D., McManus, R., Ryan, T.

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Diacetyl as a Flavor Component in Full Fat Cottage Cheese von ANTINONE, M.J., LAWLESS, H.T., LEDFORD, R.A., JOHNSTON, M.

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Loss of Trem2 in microglia leads to widespread disruption of cell coexpression networks in mouse brain von Carbajosa, G, Malki, K, Lawless, N, Wang, H, Ryder, JW, Wozniak, E, Wood, K, Mein, CA, Dobson, RJB, Collier, DA, O'Neill, MJ, Hodges, AK, Newhouse, SJ

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Role of chemotaxis in the ecology of denitrifiers von Kennedy, M.J, Lawless, J.G

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Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency von Lawless, D, Geier, CB, Farmer, JR, Lango, HA, Thwaites, D, Atschekzei, F, Brown, M, Buchbinder, D, Burns, SO, Butte, MJ, Csomos, K, Deevi, SVV, Egner, W, Ehl, S, Eibl, MM, Fadugba, O, Foldvari, Z, Green, DM, Henrickson, SE, Holland, SM, John, T, Klemann, C, Kuijpers, TW, Moreira, F, Piller, A, Rayner-Matthews, P, Romberg, ND, Sargur, R, Schmidt, RE, Schröder, C, Schuetz, C, Sharapova, SO, Smith, KGC, Sogkas, G, Speckmann, C, Stirrups, K, Thrasher, AJ, Wolf, HM, Notarangelo, LD, Anwar, R, Boyes, J, Ujhazi, B, NIHR BioResource - Rare Diseases Consortium, Thaventhiran, J, Walter, JE, Savic, S

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Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency von Lawless, D, Geier, CB, Farmer, JR, Lango Allen, H, Thwaites, D, Atschekzei, F, Brown, M, Buchbinder, D, Burns, SO, Butte, MJ, Csomos, K, Deevi, SVV, Egner, W, Ehl, S, Eibl, MM, Fadugba, O, Foldvari, Z, Green, DM, Henrickson, SE, Holland, SM, John, T, Klemann, C, Kuijpers, TW, Moreira, F, Piller, A, Rayner-Matthews, P, Romberg, ND, Sargur, R, Schmidt, RE, Schröder, C, Schuetz, C, Sharapova, SO, Smith, KGC, Sogkas, G, Speckmann, C, Stirrups, K, Thrasher, AJ, Wolf, HM, Notarangelo, LD, Anwar, R, Boyes, J, Ujhazi, B, NIHR BioResource - Rare Diseases Consortium, Thaventhiran, J, Walter, JE, Savic, S

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Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis von Lawless, M. W., White, M., Mankan, A. K., O'Dwyer, M. J., Norris, S.

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