Existence and approximation of fixed points of right Bregman nonexpansive operators

We study the existence and approximation of fixed points of right Bregman nonexpansive operators in reflexive Banach space. We present, in particular, necessary and sufficient conditions for the existence of fixed points and an implicit scheme for approximating them

Molecular line emission in NGC1068 imaged with ALMA. I An AGN-driven outflow in the dense molecular gas

We investigate the fueling and the feedback of star formation and nuclear activity in NGC1068, a nearby (D=14Mpc) Seyfert 2 barred galaxy, by analyzing the distribution and kinematics of the molecular gas in the disk. We have used ALMA to map the emission of a set of dense molecular gas tracers (CO(3-2), CO(6-5), HCN(4-3), HCO+(4-3) and CS(7-6)) and their underlying continuum emission in the central r ~ 2kpc of NGC1068 with spatial resolutions ~ 0.3"-0.5" (~ 20-35pc). Molecular line and dust continuum emissions are detected from a r ~ 200pc off-centered circumnuclear disk (CND), from the 2.6kpc-diameter bar region, and from the r ~ 1.3kpc starburst (SB) ring. Most of the emission in HCO+, HCN and CS stems from the CND. Molecular line ratios show dramatic order-of-magnitude changes inside the CND that are correlated with the UV/X-ray illumination by the AGN, betraying ongoing feedback. The gas kinematics from r ~ 50pc out to r ~ 400pc reveal a massive (M_mol ~ 2.7 (+0.9, -1.2) x 10^7 Msun) outflow in all molecular tracers. The tight correlation between the ionized gas outflow, the radio jet and the occurrence of outward motions in the disk suggests that the outflow is AGN-driven. The outflow rate estimated in the CND, dM/dt ~ 63 (+21, -37) Msun yr^-1, is an order of magnitude higher than the star formation rate at these radii, confirming that the outflow is AGN-driven. The power of the AGN is able to account for the estimated momentum and kinetic luminosity of the outflow. The CND mass load rate of the CND outflow implies a very short gas depletion time scale of <=1 Myr.Comment: Version accepted for publication in A&A (June 4th). Accepted version. References (3) added and minor typos corrected. 24 pages, 20 figure

Disease severity in familial cases of IBD

Background: Phenotypic traits of familial IBD relative to sporadic cases are controversial, probably related to limited statistical power of published evidence. Aim: To know if there are phenotype differences between familial and sporadic IBD, evaluating the prospective Spanish registry (ENEIDA) with 11,983 cases. Methods: 5783 patients (48.3%) had ulcerative colitis (UC) and 6200 (51.7%) Crohn's disease (CD). Cases with one or more 1st, 2nd or 3rd degree relatives affected by UC/CD were defined as familial case. Results: In UC and CD, familial cases compared with sporadic cases had an earlier disease onset (UC: 33 years [IQR 25–44] vs 37 years [IQR 27–49]; p b 0.0001); (CD: 27 years [IQR 21–35] vs 29 years [IQR 22–40]; p b 0.0001), higher prevalence of extraintestinal immune-related manifestations (EIMs) (UC: 17.2% vs 14%; p = 0.04); (CD: 30.1% vs 23.6%; p b 0.0001). Familial CD had higher percentage of ileocolic location (42.7% vs 51.8%; p = 0.0001), penetrating behavior (21% vs 17.6%; p = 0.01) and perianal disease (32% vs 27.1%; p = 0.003). Differences are not influenced by degree of consanguinity. Conclusion: When a sufficiently powered cohort is evaluated, familial aggregation in IBD is associated to an earlier disease onset, more EIMs and more severe phenotype in CD. This feature should be taken into account at establishing predictors of disease course

Suzaku observation of the LINER NGC 4102

Low ionisation nuclear emission-line region (LINER) nuclei have been claimed to be different than other active galactic nuclei (AGN) due to the presence of complex absorbing structures along the line-of-sight and/or an inefficient mode of accretion onto the supermassive black hole. However, this issue is still open. We have investigated the broad band X-ray spectrum of NGC 4102, one of the most luminous LINERs in the Swift/BAT survey. We studied a 80 ksec Suzaku spectrum of NGC 4102, together with archival Chandra and Swift/BAT observations. We also studied the optical (3.5m/TWIN at Calar Alto observatory) and near-infrared (WHT/LIRIS at Observatorio Roque los Muchachos) spectra that were taken contemporaneous to the Suzaku data. There is strong evidence that NGC 4102 is a Compton-thick AGN, as suggested by the Swift/BAT detected intrinsic continuum and the presence of a strong narrow, neutral FeKa emission line. We have also detected ionised FeXXV emission lines in the Suzaku spectrum of the source. NGC 4102 shows a variable soft excess found at a significantly higher flux state by the time of Suzaku observations when compared to Chandra observations. Finally, a complex structure of absorbers is seen with at least two absorbers apart from the Compton-thick one, derived from the X-ray spectral analysis and the optical extinction.Comment: 11 pages, 6 figures and 3 tables. Accepted for publication in Astronomy & Astrophysic

Mammalian Glutaminase Gls2 Gene Encodes Two Functional Alternative Transcripts by a Surrogate Promoter Usage Mechanism

Glutaminase is expressed in most mammalian tissues and cancer cells, but the regulation of its expression is poorly understood. An essential step to accomplish this goal is the characterization of its species- and cell-specific isoenzyme pattern of expression. Our aim was to identify and characterize transcript variants of the mammalian glutaminase Gls2 gene.We demonstrate for the first time simultaneous expression of two transcript variants from the Gls2 gene in human, rat and mouse. A combination of RT-PCR, primer-extension analysis, bioinformatics, real-time PCR, in vitro transcription and translation and immunoblot analysis was applied to investigate GLS2 transcripts in mammalian tissues. Short (LGA) and long (GAB) transcript forms were isolated in brain and liver tissue of human, rat and mouse. The short LGA transcript arises by a combination of two mechanisms of transcriptional modulation: alternative transcription initiation and alternative promoter. The LGA variant contains both the transcription start site (TSS) and the alternative promoter in the first intron of the Gls2 gene. The full human LGA transcript has two in-frame ATGs in the first exon, which are missing in orthologous rat and mouse transcripts. In vitro transcription and translation of human LGA yielded two polypeptides of the predicted size, but only the canonical full-length protein displayed catalytic activity. Relative abundance of GAB and LGA transcripts showed marked variations depending on species and tissues analyzed.This is the first report demonstrating expression of alternative transcripts of the mammalian Gls2 gene. Transcriptional mechanisms giving rise to GLS2 variants and isolation of novel GLS2 transcripts in human, rat and mouse are presented. Results were also confirmed at the protein level, where catalytic activity was demonstrated for the human LGA protein. Relative abundance of GAB and LGA transcripts was species- and tissue-specific providing evidence of a differential regulation of GLS2 transcripts in mammals

HLA-DRB1 association with Henoch-Schonlein purpura

Objective: Henoch-Schönlein purpura (HSP) is the most common vasculitis in children but it is not exceptional in adults. Increased familial occurrence supports a genetic predisposition for HSP. In this context, an association with the human leukocyte antigen-HLA-DRB1*01 phenotype has been suggested in Caucasian individuals with HSP. However, data on the potential association of HSP with HLA-DRB1*01 were based on small case series. To further investigate this issue, we performed HLA-DRB1 genotyping of the largest series of HSP patients ever assessed for genetic studies in Caucasians. Methods: 342 Spanish patients diagnosed with HSP fulfilling the American College of Rheumatology and the Michel et al classification criteria, and 303 sex and ethnically matched controls were assessed. HLA-DRB1 alleles were determined using a PCR-Sequence-Specific-Oligonucleotide Probe (PCR-SSOP) method. Results: A statistically significant increase of HLA-DRB1*01 in HSP patients when compared with controls was found (43% vs 7%, respectively; p<0.001; odds ratio-OR=2.03 [1.43-2.87]). It was due to the increased frequency of HLA-DRB1*0103 phenotype in HSP (14% vs 2%; p<0.001; OR=8.27 [3.46-23.9]). These results remained statistically significant after adjusting for Bonferroni correction. In contrast, a statistically significant decreased frequency of the HLA-DRB1*0301 phenotype was observed in patients compared to controls (5.6% vs 18.1%, respectively; p<0.001, OR=0.26 [0.14-0.47]), even after adjustment for Bonferroni correction. No HLA-DRB1 association with specific features of the disease was found. Conclusion: Our study confirms an association of HSP with HLA-DRB1*01 in Caucasians. Also, a protective effect against the development of HSP appears to exist in Caucasians carrying the HLA-DRB1*03 phenotype