1,046 research outputs found
Strength of the d_{x^2-y^2} pairing in the two-leg Hubbard ladder
In the ground state of the doped two-leg Hubbard ladder there are power-law
decaying d_{x^2-y^2}-type pairing correlations. It is important to know the
strength and the temperature scale of these correlations. For this purpose, we
have performed determinantal Quantum Monte Carlo (QMC) calculations of the
reducible particle-particle interaction in the Hubbard ladder. In this paper,
we report on these calculations and show that, at sufficiently low
temperatures, resonant particle-particle scattering takes place in the
d_{x^2-y^2} pairing channel for certain values of the model parameters. The QMC
data presented here indicate that the d_{x^2-y^2} pairing correlations are
strong in the Hubbard ladder.Comment: 5 pages, 5 figure
Theory of spin and charge fluctuations in the Hubbard model
A self-consistent theory of both spin and charge fluctuations in the Hubbard
model is presented. It is in quantitative agreement with Monte Carlo data at
least up to intermediate coupling . It includes both
short-wavelength quantum renormalization effects, and long-wavelength thermal
fluctuations which can destroy long-range order in two dimensions. This last
effect leads to a small energy scale, as often observed in high temperature
superconductors. The theory is conserving, satisfies the Pauli principle and
includes three-particle correlations necessary to account for the incipient
Mott transition.Comment: J1K 2R1 10 pages, Revtex 3.0, 4 uuencoded postscript figures, report#
CRPS-93-4
Nonlinear Meissner Effect in CuO Superconductors
Recent theories of the NMR in the CuO superconductors are based on a
spin-singlet order parameter. Since this state has nodal lines on
the Fermi surface, nonlinear effects associated with low-energy quasiparticles
become important, particularly at low temperatures. We show that the
field-dependence of the supercurrent, below the nucleation field for vortices,
can be used to locate the positions of the nodal lines of an unconventional gap
in momentum space, and hence test the proposed state.Comment: 5 pages (RevTex), 1 figure (postscript file incl.
Quasiparticle Dispersion of the 2D Hubbard Model: From an Insulator to a Metal
On the basis of Quantum-Monte-Carlo results the evolution of the spectral
weight of the two-dimensional Hubbard model is studied from
insulating to metallic behavior. As observed in recent photoemission
experiments for cuprates, the electronic excitations display essentially
doping-independent features: a quasiparticle-like dispersive narrow band of
width of the order of the exchange interaction and a broad valence- and
conduction-band background. The continuous evolution is traced back to one and
the same many-body origin: the doping-dependent antiferromagnetic spin-spin
correlation.Comment: 11 pages, REVtex, 4 figures (in uuencoded postscript format
Randomised field trial to evaluate serological response after foot-and-mouth disease vaccination in Turkey
AbstractDespite years of biannual mass vaccination of cattle, foot-and-mouth disease (FMD) remains uncontrolled in Anatolian Turkey. To evaluate protection after mass vaccination we measured post-vaccination antibodies in a cohort of cattle (serotypes O, A and Asia-1). To obtain results reflecting typical field protection, participants were randomly sampled from across Central and Western Turkey after routine vaccination. Giving two-doses one month apart is recommended when cattle are first vaccinated against FMD. However, due to cost and logistics, this is not routinely performed in Turkey, and elsewhere. Nested within the cohort, we conducted a randomised trial comparing post-vaccination antibodies after a single-dose versus a two-dose primary vaccination course.Four to five months after vaccination, only a third of single-vaccinated cattle had antibody levels above a threshold associated with protection. A third never reached this threshold, even at peak response one month after vaccination. It was not until animals had received three vaccine doses in their lifetime, vaccinating every six months, that most (64% to 86% depending on serotype) maintained antibody levels above this threshold. By this time cattle would be >20 months old with almost half the population below this age. Consequently, many vaccinated animals will be unprotected for much of the year. Compared to a single-dose, a primary vaccination course of two-doses greatly improved the level and duration of immunity. We concluded that the FMD vaccination programme in Anatolian Turkey did not produce the high levels of immunity required. Higher potency vaccines are now used throughout Turkey, with a two-dose primary course in certain areas.Monitoring post-vaccination serology is an important component of evaluation for FMD vaccination programmes. However, consideration must be given to which antigens are present in the test, the vaccine and the field virus. Differences between these antigens affect the relationship between antibody titre and protection
Improved metabolic control in tetrahydrobiopterin (BH4), responsive phenylketonuria with sapropterin administered in two divided doses vs. a single daily dose
Background: Phenylketonuria (PKU) often requires a lifelong phenylalanine (Phe)-restricted diet. Introduction of 6R-tetrahydrobiopterin (BH4) has made a huge difference in the diets of patients with PKU. BH4 is the co-factor of the enzyme phenylalanine hydroxylase (PAH) and improves PAH activity and, thus, Phe tolerance in the diet. A limited number of published studies suggest a pharmacodynamic profile of BH4 more suitable to be administered in divided daily doses. /
Methods: After a 72-h BH4 loading test, sapropterin was initiated in 50 responsive patients. This case-control study was conducted by administering the same daily dose of sapropterin in group 1 (n=24) as a customary single dose or in two divided doses in group 2 (n=26) over 1 year. /
Results: Mean daily consumption of Phe increased significantly after the first year of BH4 treatment in group 2 compared to group 1 (p<0.05). At the end of the first year of treatment with BH4, another dramatic difference observed between the two groups was the ability to transition to a Phe-free diet. Eight patients from group 2 and two from group 1 could quit dietary restriction. /
Conclusions: When given in two divided daily doses, BH4 was more efficacious than a single daily dose in increasing daily Phe consumption, Phe tolerance and the ability to transition to a Phe-unrestricted diet at the end of the first year of treatment
Clinical and molecular findings in 37 Turkish patients with isolated methylmalonic acidemia
BACKGROUND/AIM: Isolated methylmalonic acidemia is caused by complete or partial deficiency of the enzyme methylmalonyl-CoA mutase (mut0 or mut? enzymatic subtype), a defect of its cofactor adenosyl-cobalamin (cblA, cblB, or cblD-MMA) or deficiency of the enzyme methylmalonyl-CoA epimerase. While onset of the disease ranges from the neonatal period to adulthood, most cases present with lethargy, vomiting and ketoacidosis in the early infancy. Major secondary complications are; growth failure, developmental delay, interstitial nephritis with progressive renal failure, basal ganglia injury and cardiomyopathy. We aimed to demonstrate clinical and molecular findings based on long-term follow up in our patient cohort. MATERIALS AND METHODS: The study includes 37 Turkish patients with isolated MMA who were followed up for long term complications 1 to 14 years. All patients were followed up regularly with clinical, biochemical and dietary monitoring to determine long term complications. Next Generation Sequencing technique was used for mutation screening in five disease-causing genes including; MUT, MMAA, MMAB, MMADHC, MCEE genes. Mutation screening identified 30 different types of mutations. RESULTS: While 28 of these mutations were previously reported, one novel MMAA mutation p.H382Pfs*24 (c.1145delA) and one novel MUT mutation IVS3+1G>T(c.752+1G>T) has been reported. The most common clinical complications were growth retardation, renal involvement, mental motor retardation and developmental delay. Furthermore, one of our patients developed cardiomyopathy, another one died because of hepatic failure and one presented with lactic acidosis after linezolid exposure. CONCLUSIONS: We have detected two novel mutations, including one splice-site mutation in the MUT gene and one frame shift mutation in the MMAA gene in 37 Turkish patients. We confirm the genotype-phenotype correlation in the study population according to the long term complications
Clinical features of 27 Turkish Propionic acidemia patients with 12 novel mutations
Propionic acidemia (PA) is an inherited metabolic disease caused by the deficiency of one of the four biotin-dependent enzymes propionyl-CoA carboxylase (PCC), and is characterized by coma and death in unrecognized patients, additionally late diagnosis leads to severe developmental delay and neurological sequels. Manifestations of PA over time can include growth impairment, intellectual disability, seizures, basal ganglia lesions, pancreatitis, and cardiomyopathy. Other rarely reported complications include optic atrophy, hearing loss, premature ovarian insufficiency, and chronic renal failure. Mutations in PCCA-PCCB genes cause the clinically heterogeneous disease of PA. In this study, we investigate the mutation spectrum of PCCAPCCB genes and phenotypic features of 27 Turkish patients with PA from the South and Southeast parts of Turkey. We report 12 novel PA mutations, five affecting the PCCA gene and 7 affecting the PCCB gene
Twenty-seven mutations with three novel pathologenic variants causing biotinidase deficiency: a report of 203 patients from the southeastern part of Turkey
BACKGROUND: Biotinidase deficiency (BD) is an autosomal recessive inborn error of metabolism characterized by neurologic and cutaneous symptoms and can be detected by newborn screening. Newborn screening for BD was implemented in Turkey at the end of 2008. METHODS: In total, 203 patients who were identified among the infants detected by the newborn screening were later confirmed to have BD through measurement of serum biotinidase activity. We also performed BTD mutation analysis to characterize the genetic profile. RESULTS: Twenty-seven mutations were identified. The most commonly found variants were c.1330G>C (p.D444H), c.1595C>T (p.T532M), c.470G>A (p.R157H), and c.198_104delGCGGCTGinsTCC (p.C33Ffs ) with allele frequencies of 0.387, 0.175, 0.165 and 0.049, respectively. Three novel pathogenic and likely pathogenic variants were identified: p.W140* (c.419G>A), p.S319F (c.956C>T) and p.L69Hfs*24 (c.192_193insCATC). We also identified three mutations reported in just one patient in the past (p.V442Sfs*59 [c.1324delG], p.H447R [c.1340A>G] and p.198delV [c.592_594delGTC]). Although all of the patients were asymptomatic under the treatment of biotin, only one patient, who had the novel c.419G>A homozygous mutation became symptomatic during an episode of acute gastroenteritis with a presentation of ketosis and metabolic acidosis. Among the screened patients, 156 had partial and 47 had profound BD. CONCLUSIONS: We determined the mutation spectra of BD from the southeastern part of Turkey. The results of this study add three more mutations to the total number of mutations described as causing BD
On the Critical Behavior of the Uniform Susceptibility of a Fermi Liquid Near an Antiferromagnetic Transition with Dynamic Exponent
We compute the leading behavior of the uniform magnetic susceptibility,
, of a Fermi liquid near an antiferromagnetic transition with dynamic
exponent . Our calculation clarifies the role of triangular ``anomaly''
graphs in the theory and justifies the effective action used in previous work
\cite{Hertz}. We find that at the critical point of a two dimensional
material, with and
nonuniversal constants. For reasonable band structures we find that in a
weak coupling approximation is small and positive. Our result suggests that
the behavior observed in the quantum critical regime of underdoped high-
superconductors are difficult to explain in a theory.Comment: 12 pages, uuencoded Postscript fil
- …