The A1B2-XIA1 two-photon fluorescence excitation spectrum of 1,3-difluorobenzene / by 331021 Hollas, J. Michael, Hamdan Musa, Ridley, Trevor

Raman scattering study of GeSn under <1 0 0> and <1 1 0> uniaxial stress by An, Shu, Tai, Yeh-Chen, Lee, Kuo-Chih, Shin, Sang-Ho, Cheng, H. H., Chang, Guo-En, Kim, Munho

“…Here, we have investigated the Raman-strain function of Ge1-xSnx along <1 0 0> and <1 1 0> directions. GeSn nanomembranes (NMs) with different Sn compositions are transfer-printed on polyethylene terephthalate (PET) substrates. …”
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The role of Transforming Growth Factor (TGF) - Beta 1 Activated Kinase 1 (TAK1) in wound repair by Lam, Ivan Chee Ren

“…Transforming growth factor β–activated kinase 1 (TAK1) is a pivotal inflammatory mediator, and its expression is transiently elevated during wound healing, corresponding to the epidermal ROS production profile in the wound. …”
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Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts. by Renella, R, Roberts, N, Brown, J, De Gobbi, M, Bird, L, Hassanali, T, Sharpe, J, Sloane-Stanley, J, Ferguson, D, Cordell, J, Buckle, V, Higgs, D, Wood, W

“…Congenital dyserythropoietic anemia type 1 (CDA-1), a rare inborn anemia characterized by abnormal chromatin ultrastructure in erythroblasts, is caused by abnormalities in codanin-1, a highly conserved protein of unknown function. …”

Type 1 diabetes in mice is linked to the interleukin-1 receptor and Lsh/Ity/Bcg genes on chromosome 1. by Cornall, R, Prins, J, Todd, J, Pressey, A, DeLarato, N, Wicker, L, Peterson, L

“…Of the three diabetes-susceptibility genes, Idd-1 -3 and -4 that have been mapped in mice to date, only in the case of Idd-1 is there any evidence for the identity of the gene product: allelic variation within the murine immune response I-A beta gene and its human homologue HLA-DQB1 correlates with susceptibility, implying that I-A beta is a component of Idd-1. …”

Proceedings: Some effects of disodium ethane-1-hydroxy-1,1-diphosphonate (EHDP) on calcium metabolism in man. by Walton, R, Russell, R, Smith, R, Warner, G

Synthesis of all-carbon disubstituted bicyclo[1.1.1]pentanes by iron-catalyzed Kumada cross-coupling by Nugent, J, Shire, BR, Caputo, DFJ, Pickford, HD, Nightingale, F, Houlsby, ITT, Mousseau, JJ, Anderson, EA

“…1,3-Disubstituted bicyclo[1.1.1]pentanes (BCPs) are important motifs in drug design as surrogates for p-substituted arenes and alkynes. …”

Modulation of the IL-1 cytokine network in keratinocytes by intracellular IL-1 alpha and IL-1 receptor antagonist. by Phillips, W, Feldmann, M, Breathnach, S, Brennan, F

“…Intracellular (ic) IL-1 alpha and IL-1 receptor antagonist protein (IL-1Ra) following cell lysis were readily identified assayed using a capture ELISA; whereas in culture supernatants IL-1Ra was not detected, and IL-1 alpha was present at only very low levels. …”

The European Consortium on MEN1 - Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1) by Bassett, J, Pannett, A, Forbes, SA, Thakker, R, McCarthy, M, Read, A, Teh, B, Larsson, C, Kytola, S, Leisti, J, Salmela, P, Weber, G, Giraud, S, Zhang, C, Calender, A, Hoppener, J, vanAmstel, H, Lips, C, Kas, K, VandeVen, W, Gaudray, P

Cicero, De Inuentione, Book 1: Introduction and commentary (1.19b-33; 1.97-109) by Hirsch, T

“…</p> <p>The structure of the commentary on each of these sections will be: introduction to the section, references to parallel passages in other Latin and Greek rhetorical texts, the most important general literature on the subject of the section, comparison of the passage in Cic.<em>Inu</em>.1 with the corresponding one in <em>Rhet.Her</em>, individual lemmata. …”

Codanin-1 Mutations In Congenital Dyserythropoietic Anemia Type 1 Affect HP1 alpha Localization In Erythroblasts by Renella, R, Roberts, N, Brown, J, De Gobbi, M, Bird, L, Hassanali, T, Sloane-Stanley, J, Sharpe, J, Cordell, J, Ferguson, D, Buckle, V, Higgs, D, Wood, W

Synthesis of all‐carbon disubstituted bicyclo[1.1.1]pentanes by iron‐catalyzed Kumada cross‐coupling by Nugent, J, Shire, B, Caputo, DFJ, Pickford, HD, Nightingale, F, Houlsby, I, Mousseau, J, Anderson, EA

“…1,3‐Disubstituted bicyclo[1.1.1]pentanes (BCPs) are important motifs in drug design as surrogates for p‐substituted arenes and alkynes. …”

BIFUNCTIONAL CHIRAL AUXILIARIES .2. THE SYNTHESIS OF 1,3-DIACYLIMIDAZOLIDIN-2-ONES FROM 1,2-DIAMINES by Davies, S, Mortlock, A

Altered hippocampal gene expression and structure in transgenic mice overexpressing neuregulin 1 (Nrg1) type I by Deakin, I, Godlewska, B, Walker, M, Huang, G, Schwab, M, Nave, K, Law, A, Harrison, P

“…Transgenic mice overexpressing the type I isoform of neuregulin 1 (Nrg1; NRG1) have alterations in hippocampal gamma oscillations and an age-emergent deficit in hippocampus-dependent spatial working memory. …”

The European Consortium on MEN1. Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1). by Bassett, J, Pannett, A, Forbes, SA, Thakker, R, McCarthy, M, Read, A, Teh, B, Larsson, C, Kytölä, S, Leisti, J, Salmela, P, Weber, G, Giraud, S, Zhang, C, Calender, A, Höppener, J, Ploos van Amstel, H, Lips, C, Kas, K, Van de Yen, W, Gaudray, P

“…Such studies may have a limited resolution of approximately 1 cM (i.e. 1 Mb) and we have therefore investigated 96 MEN1 families (40 British, 17 French, 12 Finnish, 7 Swedish, 7 Dutch, 7 North American, 2 Australian, 1 New Zealand, 1 German, 1 Spanish and 1 Danish) for linkage disequilibrium, in order to facilitate a finer mapping resolution. …”

The genomic landscape of the somatic linker histone subtypes H1.1 to H1.5 in human cells. by Izzo, A, Kamieniarz-Gdula, K, Ramírez, F, Noureen, N, Kind, J, Manke, T, van Steensel, B, Schneider, R

“…Human cells contain five canonical, replication-dependent somatic histone H1 subtypes (H1.1, H1.2, H1.3, H1.4, and H1.5). …”

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1 alpha localization in erythroblasts by Renella, R, Roberts, N, Brown, J, De Gobbi, M, Bird, L, Hassanali, T, Sharpe, J, Sloane-Stanley, J, Ferguson, D, Cordell, J, Buckle, V, Higgs, D, Wood, W

“…Congenital dyserythropoietic anemia type 1 (CDA-1), a rare inborn anemia characterized by abnormal chromatin ultrastructure in erythroblasts, is caused by abnormalities in codanin-1, a highly conserved protein of unknown function. …”

Caveolin-1 and lipid rafts in confluent BeWo trophoblasts: evidence for Rock-1 association with caveolin-1. by Rashid-Doubell, F, Tannetta, D, Redman, C, Sargent, I, Boyd, C, Linton, E

“…This close association of plasmalemmal caveolin-1 with Rock-1 protein raises the possibility that caveolin-1 may regulate Rock-1 in these trophoblasts. …”

The Genomic Landscape of the Somatic Linker Histone Subtypes H1.1 to H1.5 in Human Cells by Izzo, A, Kamieniarz-Gdula, K, Ramírez, F, Noureen, N, Kind, J, Manke, T, vanSteensel, B, Schneider, R

“…Human cells contain five canonical, replication-dependent somatic histone H1 subtypes (H1.1, H1.2, H1.3, H1.4, and H1.5). …”

(3E)-3-[4-(Dimethylamino)phenyl]-1-(4-hydroxyphenyl)prop-2-en-1-one by Hasan, A., Akhtar, N., Lajis, N., Rusli, A.F., Lo, K.M.