6 research outputs found
Increased localization of Majorana modes in antiferromagnetic chains on superconductors
Magnet-superconductor hybrid (MSH) systems are a key platform for
custom-designed topological superconductors. Ideally, the ends of a
one-dimensional MSH structure will host Majorana zero-modes (MZMs), the
fundamental unit of topological quantum computing. However, some of the
experiments with ferromagnetic chains show a more complicated picture. Due to
tiny gap sizes and hence long coherence lengths MZMs might hybridize and lose
their topological protection. Recent experiments on a niobium surface have
shown that both ferromagnetic and antiferromagnetic chains may be engineered,
with the magnetic order depending on the crystallographic direction of the
chain. While ferromagnetic chains are well understood, antiferromagnetic chains
are less so. Here we study two models inspired by the niobium surface: a
minimal model to elucidate the general topological properties of
antiferromagnetic chains, and an extended model to more closely simulate a real
system by mimicking the proximity effect. We find that in general for
antiferromagnetic chains the topological gap is larger than for ferromagnetic
ones and thus coherence lengths are shorter for antiferromagnetic chains,
yielding more pronounced localization of MZMs in these chains. While
topological phases for both ferromagnetic and antiferromagnetic chains both
depend on the magnetic moment of the adatoms and the chemical potential, we
find that antiferromagnetic chains also have a strong dependence on the
magnitude of Rashba spin-orbit coupling at the surface.Comment: 12 pages,11 figure
Early onset lung cancer, cigarette smoking and the SNP309 of the murine double minute-2 (MDM2) gene
The polymorphism SNP309 (rs2279744) in the promoter region of the MDM2 gene has been shown to alter protein expression and may play a role in the susceptibility to lung cancer. The MDM2 protein is a key inhibitor of p53 and several mechanisms of MDM2/p53 interactions are presently known: modulating DNA-repair, cell-cycle control, cell growth and apoptosis
Do genetic factors protect for early onset lung cancer? A case control study before the age of 50 years
<p>Abstract</p> <p>Background</p> <p>Early onset lung cancer shows some familial aggregation, pointing to a genetic predisposition. This study was set up to investigate the role of candidate genes in the susceptibility to lung cancer patients younger than 51 years at diagnosis.</p> <p>Methods</p> <p>246 patients with a primary, histologically or cytologically confirmed neoplasm, recruited from 2000 to 2003 in major lung clinics across Germany, were matched to 223 unrelated healthy controls. 11 single nucleotide polymorphisms of genes with reported associations to lung cancer have been genotyped.</p> <p>Results</p> <p>Genetic associations or gene-smoking interactions was found for <it>GPX1(Pro200Leu) </it>and <it>EPHX1(His113Tyr)</it>. Carriers of the Leu-allele of <it>GPX1(Pro200Leu) </it>showed a significant risk reduction of OR = 0.6 (95% CI: 0.4–0.8, p = 0.002) in general and of OR = 0.3 (95% CI:0.1–0.8, p = 0.012) within heavy smokers. We could also find a risk decreasing genetic effect for His-carriers of <it>EPHX1(His113Tyr) </it>for moderate smokers (OR = 0.2, 95% CI:0.1–0.7, p = 0.012). Considered both variants together, a monotone decrease of the OR was found for smokers (OR of 0.20; 95% CI: 0.07–0.60) for each protective allele.</p> <p>Conclusion</p> <p>Smoking is the most important risk factor for young lung cancer patients. However, this study provides some support for the T-Allel of <it>GPX1(Pro200Leu) </it>and the C-Allele of <it>EPHX1(His113Tyr) </it>to play a protective role in early onset lung cancer susceptibility.</p