Search results for "3S"
showing 10 items of 133 documents
"Table 3" of "Inclusive $\Upsilon$ production in p-Pb collisions at $\sqrt{s_{\rm NN}}$ = 8.16 TeV"
2020
$\Upsilon$(3S) differential cross section as a function of $y_{\rm cms}$, in p--Pb collisions at $\sqrt{s_{\rm NN}}$ = 8.16 TeV. The first uncertainty is statistical, while the second is the systematic.
"Table 16" of "Inclusive $\Upsilon$ production in p-Pb collisions at $\sqrt{s_{\rm NN}}$ = 8.16 TeV"
2020
$\Upsilon$(3S) $R_{\rm pPb}$ values at $\sqrt{s_{\rm NN}}$ = 8.16 TeV. The first uncertainty is statistical, the second is the uncorrelated systematic, while the third one is a correlated systematic uncertainty.
"Table 7" of "Inclusive $\Upsilon$ production in p-Pb collisions at $\sqrt{s_{\rm NN}}$ = 8.16 TeV"
2020
Ratio of $\Upsilon$(3S) over $\Upsilon$(1S) yields in p--Pb collisions at $\sqrt{s_{\rm NN}}$ = 8.16 TeV .The first uncertainty is statistical, while the second is the systematic.
"Table 4" of "Production of Lambda, Cascade and Omega Hyperons in ppbar Collisions at1.96 TeV Center of Mass Energy"
2011
The PT differential cross section for XI- production in two charged-particle multiplicty regions.
"Table 1" of "Production of Lambda, Cascade and Omega Hyperons in ppbar Collisions at1.96 TeV Center of Mass Energy"
2011
The PT differential cross section for LAMBBA production in the |pseudorapidity| range < 1.
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2
2020
Alternating Hemiplegia of Childhood (AHC) is a rare disorder characterized by frequent, transient attacks of hemiplegia involving either side of the body or both in association to several other disturbances including dystonic spells, abnormal ocular movements, autonomic manifestations, epileptic seizures and cognitive impairment. The clinical manifestations usually start before the age of 18 months. Two forms of the disorder known as AHC-1 (MIM#104290) and AHC-2 (MIM#614820) depends on mutations in ATP1A2 and ATP1A3 genes respectively, with over 75% of AHC caused by a mutation in the ATP1A3 gene. Herewith, we report serial clinical follow-up data of monozygotic (MZ) twin sisters, who presen…
"Table 4" of "Quasi-free Compton Scattering and the Polarizabilities of the Neutron"
2003
Energy dependence of the triple differential cross section w.r.t. the scattered neutron.
"Table 3" of "Quasi-free Compton Scattering and the Polarizabilities of the Neutron"
2003
Energy dependence of the triple differential cross section w.r.t. the scattered proton.
Partial Methylation at Am100 in 18S rRNA of Baker's Yeast Reveals Ribosome Heterogeneity on the Level of Eukaryotic rRNA Modification
2014
Ribosome heterogeneity is of increasing biological significance and several examples have been described for multicellular and single cells organisms. In here we show for the first time a variation in ribose methylation within the 18S rRNA of Saccharomyces cerevisiae. Using RNA-cleaving DNAzymes, we could specifically demonstrate that a significant amount of S. cerevisiae ribosomes are not methylated at 2'-O-ribose of A100 residue in the 18S rRNA. Furthermore, using LC-UV-MS/MS of a respective 18S rRNA fragment, we could not only corroborate the partial methylation at A100, but could also quantify the methylated versus non-methylated A100 residue. Here, we exhibit that only 68% of A100 in t…
CCDC 689575: Experimental Crystal Structure Determination
2009
Related Article: J.L.G.Ruano, J.Aleman, S.Catalan, V.Marcos, S.Monteagudo, A.Parra, C.del Pozo, S.Fustero|2008|Angew.Chem.,Int.Ed.|47|7941|doi:10.1002/anie.200802885