118 research outputs found
Self-similarity and singularity formation in a coupled system of Yang-Mills-dilaton evolution equations
We study both analytically and numerically a coupled system of spherically
symmetric SU(2) Yang-Mills-dilaton equation in 3+1 Minkowski space-time. It has
been found that the system admits a hidden scale invariance which becomes
transparent if a special ansatz for the dilaton field is used. This choice
corresponds to transition to a frame rotated in the plane at a
definite angle. We find an infinite countable family of self-similar solutions
which can be parametrized by the - the number of zeros of the relevant
Yang-Mills function. According to the performed linear perturbation analysis,
the lowest solution with N=0 only occurred to be stable. The Cauchy problem has
been solved numerically for a wide range of smooth finite energy initial data.
It has been found that if the initial data exceed some threshold, the resulting
solutions in a compact region shrinking to the origin, attain the lowest N=0
stable self-similar profile, which can pretend to be a global stable attractor
in the Cauchy problem. The solutions live a finite time in a self-similar
regime and then the unbounded growth of the second derivative of the YM
function at the origin indicates a singularity formation, which is in agreement
with the general expectations for the supercritical systems.Comment: 10 pages, 5 figure
Neutron star in presence of torsion-dilaton field
We develop the general theory of stars in Saa's model of gravity with
propagating torsion and study the basic stationary state of neutron star. Our
numerical results show that the torsion force decreases the role of the gravity
in the star configuration leading to significant changes in the neutron star
masses depending on the equation of state of star matter. The inconsistency of
the Saa's model with Roll-Krotkov-Dicke and Braginsky-Panov experiments is
discussed.Comment: 29 pages, latex, 24 figures, final version. Added: 1)comments on
different possible mass definitions; 2)new sections: a)the inconsistency of
the Saa's model with Roll-Krotkov-Dicke and Braginsky-Panov experiments;
b)stability analysis via catastrophe theory; 3)new figers added and some
figures replaced. 4)new reference
Boson stars in massive dilatonic gravity
We study equilibrium configurations of boson stars in the framework of a
class scalar-tensor theories of gravity with massive gravitational scalar
(dilaton). In particular we investigate the influence of the mass of the
dilaton on the boson star structure. We find that the masses of the boson stars
in presence of dilaton are close to those in general relativity and they are
sensitive to the ratio of the boson mass to the dilaton mass within a typical
few percent. It turns out also that the boson star structure is mainly
sensitive to the mass term of the dilaton potential rather to the exact form of
the potential.Comment: 9 pages, latex, 9 figures, one figure dropped, new comments added,
new references added, typos correcte
Genome-wide expression profiling of urinary bladder implicates desmosomal and cytoskeletal dysregulation in the bladder exstrophy-epispadias complex
The bladder exstrophy-epispadias complex (BEEC) represents a spectrum of urological abnormalities where part, or all, of the distal urinary tract fails to close during development, becoming exposed on the outer abdominal wall. While the etiology of BEEC remains unknown, strong evidence exists that genetic factors are implicated. To understand the pathways regulating embryonic bladder development and to identify high-probability BEEC candidate genes, we conducted a genome-wide expression profiling (GWEP) study using normal and exstrophic human urinary bladders and human and mouse embryologic bladder-precursor tissues. We identified 162 genes differentially expressed in both embryonic and postnatal human samples. Pathway analysis of these genes revealed 11 biological networks with top functions related to skeletal and muscular system development, cellular assembly and development, organ morphology, or connective tissue disorders. The two most down-regulated genes desmin (DES, fold-change, -74.7) and desmuslin (DMN, fold-change, -53.0) are involved in desmosome mediated cell-cell adhesion and cytoskeletal architecture. Intriguingly, the sixth most overexpressed gene was desmoplakin (DSP, fold-change, +48.8), the most abundant desmosomal protein. We found 30% of the candidate genes to be directly associated with desmosome structure/function or cytoskeletal assembly, pointing to desmosomal and/or cytoskeletal deregulation as an etiologic factor for BEEC. Further findings indicate that p63, PERP, SYNPO2 and the Wnt pathway may also contribute to BEEC etiology. This study provides the first expression profile of urogenital genes during bladder development and points to the high-probability candidate genes for BEEC
Targeted Sequencing of Candidate Regions Associated with Sagittal and Metopic Nonsyndromic Craniosynostosis
Craniosynostosis (CS) is a major birth defect in which one or more skull sutures fuse prematurely. We previously performed a genome-wide association study (GWAS) for sagittal nonsyndromic CS (sNCS), identifying associations downstream from BMP2 on 20p12.3 and intronic to BBS9 on 7p14.3; analyses of imputed variants in DLG1 on 3q29 were also genome-wide significant. We followed this work with a GWAS for metopic non-syndromic NCS (mNCS), discovering a significant association intronic to BMP7 on 20q13.31. In the current study, we sequenced the associated regions on 3q29, 7p14.3, and 20p12.3, including two candidate genes (BMP2 and BMPER) near some of these regions in 83 sNCS child-parent trios, and sequenced regions on 7p14.3 and 20q13.2-q13.32 in 80 mNCS child-parent trios. These child-parent trios were selected from the original GWAS co-horts if the probands carried at least one copy of the top associated GWAS variant (rs1884302 C allele for sNCS; rs6127972 T allele for mNCS). Many of the variants sequenced in these targeted regions are strongly predicted to be within binding sites for transcription factors involved in crani-ofacial development or bone morphogenesis. Variants enriched in more than one trio and predicted to be damaging to gene function are prioritized for functional studies
Effects of Thyroxine Exposure on Osteogenesis in Mouse Calvarial Pre-Osteoblasts
The incidence of craniosynostosis is one in every 1,800-2500 births. The gene-environment model proposes that if a genetic predisposition is coupled with environmental exposures, the effects can be multiplicative resulting in severely abnormal phenotypes. At present, very little is known about the role of gene-environment interactions in modulating craniosynostosis phenotypes, but prior evidence suggests a role for endocrine factors. Here we provide a report of the effects of thyroid hormone exposure on murine calvaria cells. Murine derived calvaria cells were exposed to critical doses of pharmaceutical thyroxine and analyzed after 3 and 7 days of treatment. Endpoint assays were designed to determine the effects of the hormone exposure on markers of osteogenesis and included, proliferation assay, quantitative ALP activity assay, targeted qPCR for mRNA expression of Runx2, Alp, Ocn, and Twist1, genechip array for 28,853 targets, and targeted osteogenic microarray with qPCR confirmations. Exposure to thyroxine stimulated the cells to express ALP in a dose dependent manner. There were no patterns of difference observed for proliferation. Targeted RNA expression data confirmed expression increases for Alp and Ocn at 7 days in culture. The genechip array suggests substantive expression differences for 46 gene targets and the targeted osteogenesis microarray indicated 23 targets with substantive differences. 11 gene targets were chosen for qPCR confirmation because of their known association with bone or craniosynostosis (Col2a1, Dmp1, Fgf1, 2, Igf1, Mmp9, Phex, Tnf, Htra1, Por, and Dcn). We confirmed substantive increases in mRNA for Phex, FGF1, 2, Tnf, Dmp1, Htra1, Por, Igf1 and Mmp9, and substantive decreases for Dcn. It appears thyroid hormone may exert its effects through increasing osteogenesis. Targets isolated suggest a possible interaction for those gene products associated with calvarial suture growth and homeostasis as well as craniosynostosis. © 2013 Cray et al
Estimation of parameters in a structured SIR model
[EN] In this paper, an age-structured epidemiological process is considered. The disease
model is based on a SIR model with unknown parameters. We addressed two
important issues to analyzing the model and its parameters. One issue is concerned
with the theoretical existence of unique solution, the identifiability problem. The
second issue is how to estimate the parameters in the model. We propose an iterative
algorithm to study the identifiability of the system and a method to estimate the
parameters which are identifiable. A least squares approach based on a finite set of
observations helps us to estimate the initial values of the parameters. Finally, we test
the proposed algorithms.The authors would like to thank the referees and the editor for their comments and useful suggestions for improvement of the manuscript. This work has been partially supported by Spanish Grant MTM2013-43678-P.Cantó Colomina, B.; Coll, C.; Sánchez, E. (2017). Estimation of parameters in a structured SIR model. Advances in Difference Equations. 33:1-13. https://doi.org/10.1186/s13662-017-1078-5S11333Strogatz, S, Friedman, M, Mallinck-Rodt, AJ, McKay, S: Nonlinear Dynamics and Chaos: With Applications to Physics, Biology, Chemistry, and Engineering. Perseus Books, Washington (1994)De La Sen, M, Quesada, A: Some equilibrium, stability, instability and oscillatory results for an extended discrete epidemic model with evolution memory. Adv. Differ. Equ. 2013, 234 (2013)Han, Q, Wang, Z: On extinction of infectious diseases for multi-group SIRS models with satured incidence rate. Adv. Differ. Equ. 2015, 333 (2015)Cantó, B, Coll, C, Sánchez, E: Structural identifiability of a model of dialysis. Math. Comput. Model. 50, 733-737 (2009)Cantó, B, Coll, C, Sánchez, E: Identifiability of a class of discretized linear partial differential algebraic equations. Math. Probl. Eng., 1-12 (2011)Craciun, G, Pantea, C: Identifiability of chemical reaction networks. J. Math. Chem. 44, 244-259 (2008)Malik, MB, Salman, M: State-space least mean square. Digit. Signal Process. 18, 334-345 (2008)Ding, F, Liu, PX, Liu, G: Multiinnovatiovation least-squares identification for system modeling. IEEE Trans. Syst. Man Cybern., Part B, Cybern. 18(3), 767-778 (2010)Ben-Zvi, A, McLellan, PJ, McAuley, KB: Identifiability of linear time-invariant differential-algebraic systems, I. The generalized Markov parameter approach. Ind. Eng. Chem. Res. 42, 6607-6618 (2003)Boyadjiev, C, Dimitrova, E: An iterative method for model parameter identification. Comput. Chem. Eng. 29, 941-948 (2005)Ben-Zvi, A, McLellan, PJ, McAuley, KB: Identifiability of linear time-invariant differential-algebraic systems, 2. The differential-algebraic approach. Ind. Eng. Chem. Res. 43, 1251-1259 (2004)Dion, JM, Commault, C, van der Woude, J: Generic properties and control of linear structured systems: a survey. Automatica 39, 1125-1144 (2003)Chou, IC, Voit, EO: Recent developments in parameter estimation and structure identification of biochemical and genomic systems. Math. Biosci. 219, 57-83 (2009)Schmitz, OJ: Ecology and Ecosystems Conservation. Island Press, Washington (2013
Rare exonic CELSR3 variants identified in Bladder Exstrophy Epispadias Complex
Introduction/backgroundBladder exstrophy epispadias complex (BEEC) is a rare congenital anomaly of unknown etiology, although, genetic and environmental factors have been associated with its development. Variants in several genes expressed in the urogenital pathway have been reported as causative for bladder exstrophy in human and murine models. The expansion of next-generation sequencing and molecular genomics has improved our ability to identify the underlying genetic causes of similarly complex diseases and could thus assist with the investigation of the molecular basis of BEEC.ObjectiveThe objective was to identify the presence of rare heterozygous variants in genes previously implicated in bladder exstrophy and correlate them with the presence or absence of bladder regeneration in our study population.Patients and MethodsWe present a case series of 12 patients with BEEC who had bladder biopsies performed by pediatric urology during bladder neck reconstruction or bladder augmentation. Cases were classified as “sufficient” or “insufficient” (n = 5 and 7, respectively) based on a bladder volume of greater than or less than 40% of expected bladder size. Control bladder tissue specimens were obtained from patients (n = 6) undergoing biopsies for conditions other than bladder exstrophy. Whole exome sequencing was performed on DNA isolated from the bladder specimens. Based on the hypothesis of de novo mutations, as well as the potential implications of autosomal dominant conditions with incomplete penetrance, each case was evaluated for autosomal dominant variants in a set of genes previously implicated in BEEC.ResultsOur review of the literature identified 44 genes that have been implicated in human models of bladder exstrophy. Our whole exome sequencing data analysis identified rare variants in two of these genes among the cases classified as sufficient, and seven variants in five of these genes among the cases classified as insufficient.ConclusionWe identified rare variants in seven previously implicated genes in our BEEC specimens. Additional research is needed to further understand the cellular signaling underlying this potentially genetically heterogeneous embryological condition
Compound heterozygous variants in NBAS as a cause of atypical osteogenesis imperfecta
Background
Osteogenesis imperfecta (OI), the commonest inherited bone fragility disorder, affects 1 in 15,000 live births resulting in frequent fractures and reduced mobility, with significant impact on quality of life. Early diagnosis is important, as therapeutic advances can lead to improved clinical outcome and patient benefit.
Report
Whole exome sequencing in patients with OI identified, in two patients with a multi-system phenotype, compound heterozygous variants in NBAS (neuroblastoma amplified sequence). Patient 1: NBAS c.5741G > A p.(Arg1914His); c.3010C > T p.(Arg1004*) in a 10-year old boy with significant short stature, bone fragility requiring treatment with bisphosphonates, developmental delay and immunodeficiency. Patient 2: NBAS c.5741G > A p.(Arg1914His); c.2032C > T p.(Gln678*) in a 5-year old boy with similar presenting features, bone fragility, mild developmental delay, abnormal liver function tests and immunodeficiency.
Discussion
Homozygous missense NBAS variants cause SOPH syndrome (short stature; optic atrophy; Pelger-Huet anomaly), the same missense variant was found in our patients on one allele and a nonsense variant in the other allele. Recent literature suggests a multi-system phenotype. In this study, patient fibroblasts have shown reduced collagen expression, compared to control cells and RNAseq studies, in bone cells show that NBAS is expressed in osteoblasts and osteocytes of rodents and primates. These findings provide proof-of-concept that NBAS mutations have mechanistic effects in bone, and that NBAS variants are a novel cause of bone fragility, which is distinguishable from ‘Classical’ OI.
Conclusions
Here we report on variants in NBAS, as a cause of bone fragility in humans, and expand the phenotypic spectrum associated with NBAS. We explore the mechanism underlying NBAS and the striking skeletal phenotype in our patients
Boson-fermion stars: exploring different configurations
We use the flexibility of the concept of a fermion-boson star to explore
different configurations, ranging from objects of atomic size and masses of the
order g, up to objects of galactic masses and gigantic halos around a
smaller core, with possible interesting applications to astrophysics and
cosmology, particularly in the context of dark matter.Comment: 8 pages. Minor changes, new reference added and a few typos correcte
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