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Did you mean: person:(solis, E.) • person:(hollis, E.) • person:(collis, E.) • person:(soltis, E.) • person:(sallis, E.)
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A Cautionary Note on the Order of Integration of Post-war Aggregate Wage, Price and Productivity Measures
Online Contents | 2004|Contributors: Wohar, Mark E. -
Functional characterization of TBR1 variants in neurodevelopmental disorder
Free accessBASE | 2018| -
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders
British Library Online Contents | 2018| -
Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo-obstruction
British Library Online Contents | 2018| -
P3.32 The molecular genetics of monogenic neuromuscular disorders characterised by reduced foetal movement
British Library Online Contents | 2011| -
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder
British Library Online Contents | 2016| -
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders
British Library Online Contents | 2018| -
2,5-Diketopiperazines as Potent, Selective, and Orally Bioavailable Oxytocin Antagonists. 2. Synthesis, Chirality, and Pharmacokinetics
American Chemical Society | 2005| -
2,5-Diketopiperazines as Potent, Selective, and Orally Bioavailable Oxytocin Antagonists. 3. Synthesis, Pharmacokinetics, and in Vivo Potency
British Library Online Contents | 2006| -
ARTICLES - U.S. and U.K. Interest Rates, 1890-1934: New Evidence on Structural Breaks
Online Contents | 2001|Contributors: Sollis, Robert, Wohar, Mark E. -
Synthesis and Structure–Activity Relationships of Indazole Arylsulfonamides as Allosteric CC-Chemokine Receptor 4 (CCR4) Antagonists
American Chemical Society | 2013| -
Pyridyl-2,5-Diketopiperazines as Potent, Selective, and Orally Bioavailable Oxytocin Antagonists: Synthesis, Pharmacokinetics, and In Vivo Potency
Online Contents | 2012|Contributors: Davies, Dave E., Smith, Ian E. D., Sollis, Steve L. -
The discovery of GSK221149A: A potent and selective oxytocin antagonist
Online Contents | 2008|Contributors: Davies, David E., Sollis, Steve L. -
The Discovery of Phthalazinone-Based Human H1 and H3 Single-Ligand Antagonists Suitable for Intranasal Administration for the Treatment of Allergic Rhinitis
Online Contents | 2011|Contributors: Looker, Brian E., Sollis, Steven L. -
Synthesis and Structure–Activity Relationships of Indazole Arylsulfonamides as Allosteric CC-Chemokine Receptor 4 (CCR4) Antagonists
Online Contents | 2013|Contributors: Smith, Claire E., Sollis, Steven L.
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