Showing results 91019 to 91038 of 91414
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| Preview | Issue Date | Title | Author(s) |
| 2008 | WS3 - International workshop on context-enabled source and service selection, integration and adaptation (CSSSIA 2008) | Sheng, Q.; Srivastava, B.; Nambiar, U.; Maamr, Z.; Sheth, A.; Elnaffar, S.; International conference on the world wide web (17th : 2008 : Beijing, China) |
| 2012 | WT1 expression as a marker of minimal residual disease predicts outcome in acute myeloid leukemia when measured post-consolidation | Gray, J.; McMillen, L.; Mollee, P.; Paul, S.; Lane, S.; Bird, R.; Gill, D.; Saal, R.; Marlton, P. |
| 2016 | WTO accession and efficiency gains: Evidence from China’s banking sector | Du, K.; Andressen, C. |
| 2006 | WTO’s cotton initiative: Two complementary opportunities to boost African cotton investment, incomes and exports | Anderson, K.; Valenzuela, E.; Corporate Council on Africa¿s Private Sector Report to the AGOA Ministerial Forum (5 Jun 2006 : Washington DC) |
| 2009 | Wunderkidz in a blunderland: Tensions and tales from Sri Lankan cricket | Roberts, M. |
| 2009 | Wurm, Stephen Adolphe | Mühlhäusler, P. |
| 2007 | WUSCHEL regulates cell differentiation during anther development | Deyhle, F.; Sarkar, A.; Tucker, E.; Laux, T. |
| 2015 | WWOX, the chromosomal fragile site FRA16D spanning gene: its role in metabolism and contribution to cancer | Richards, R.I.; Choo, A.; Lee, C.S.; Dayan, S.; O Keefe, L. |
| 2006 | Wytyczne postępowania z osteoporozą omenopauzalną dla lekarzy rodzinnych | O'Neill, S.; MacLennan, A.; Bass, S.; Diamond, T.; Ebeling, P.; Findlay, D.; Flicker, L.; Markwell, A.; Nowson, C.; Pocock, N.; Sambrook, P.; Fiatarone-Singh, M. |
| 2012 | Wzy-dependent bacterial capsules as potential drug targets | Ericsson, D.; Standish, A.; Kobe, B.; Morona, R. |
| 2016 | X chromosome dose and sex bias in autoimmune diseases: increased prevalence of 47,XXX in systemic lupus erythematosus and Sjögren's syndrome | Liu, K.; Kurien, B.; Zimmerman, S.; Kaufman, K.; Taft, D.; Kottyan, L.; Lazaro, S.; Weaver, C.; Ice, J.; Adler, A.; Chodosh, J.; Radfar, L.; Rasmussen, A.; Stone, D.; Lewis, D.; Li, S.; Koelsch, K.; Igoe, A.; Talsania, M.; Kumar, J.; et al. |
| 1995 | X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome | Gedeon, A.; Wilson, M.; Colley, A.; Sillence, D.; Mulley, J. |
| 2016 | X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes | Hu, H.; Haas, S.; Chelly, J.; Van Esch, H.; Raynaud, M.; De Brouwer, A.; Weinert, S.; Froyen, G.; Frints, S.; Laumonnier, F.; Zemojtel, T.; Love, M.; Richard, H.; Emde, A.; Bienek, M.; Jensen, C.; Hambrock, M.; Fischer, U.; Langnick, C.; Feldkamp, M.; et al. |
| 2011 | X-Field exhibition | Russell-Clarke, J. |
| 1999 | X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisation | Woffendin, H.; Jakins, T.; Jouet, M.; Stewart, H.; Landy, S.; Haan, E.; Harris, A.; Donnai, D.; Read, A.; Kenwrick, S. |
| 1998 | X-linked adrenoleukodystrophy: the Australasian experience | Kirk, E.; Fletcher, J.; Sharp, P.; Carey, B.; Poulos, A. |
| 2017 | X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1 | Miyake, N.; Wolf, N.; Cayami, F.; Crawford, J.; Bley, A.; Bulas, D.; Conant, A.; Bent, S.; Gripp, K.; Hahn, A.; Humphray, S.; Kimura-Ohba, S.; Kingsbury, Z.; Lajoie, B.; Lal, D.; Micha, D.; Pizzino, A.; Sinke, R.; Sival, D.; Stolte-Dijkstra, I.; et al. |
| 2013 | X-linked inhibitor of apoptosis single nucleotide polymorphisms and copy number variation are not risk factors for asthma | Roscioli, E.; Hamon, R.; Ruffin, R.; Zalewski, P.; Grant, J.; Lester, S. |
| 2017 | X-Linked lissencephaly with absent corpus callosum and abnormal genitalia: an evolving multisystem syndrome with severe congenital intestinal diarrhea disease | Coman, D.; Fullston, T.; Shoubridge, C.; Leventer, R.; Wong, F.; Nazaretian, S.; Simpson, I.; Gecz, J.; McGillivray, G. |
| 2003 | X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in PAK3 | Gedeon, A.; Nelson, J.; Gecz, J.; Mulley, J. |
