À la suite d’une stimulation antigénique, les lymphocytes T CD8+

À la suite d’une stimulation antigénique, les lymphocytes T CD8+ naïfs Etoposide prolifèrent grâce à des molécules de co-activation clé comme en particulier le CD28. Ces lymphocytes T se différencient alors en lymphocytes T cytotoxiques

(qui meurent par apoptose après qu’ils aient accompli leurs fonctions effectrices) et en lymphocytes T mémoires effecteurs ou centraux, qui sont générés en plus petite quantité (5–10 % de la quantité initiale) et dont la fonction est d’assurer une réponse immunitaire plus rapide et plus agressive lors d’une nouvelle rencontre avec l’antigène. Les lymphocytes T CD8+ centraux ont des propriétés d’autorenouvellement. Ainsi, une nouvelle stimulation par les antigènes qu’ils reconnaissent aboutit à la génération de nouveaux lymphocytes T cytotoxiques ainsi qu’à de nouveaux lymphocytes T mémoires centraux et effecteurs. À l’inverse, la stimulation des lymphocytes T mémoires effecteurs aboutit à une prolifération plus modeste avec la mise en jeu rapide des fonctions

effectrices (cytotoxiques ou régulatrices) selleck chemicals llc [15]. Au cours d’une stimulation antigénique persistante au cours du temps, plusieurs de ces cycles d’activation surviennent, aboutissant à des stimulations/proliférations répétées. Dans ce contexte, l’expression du CD28 à la surface des lymphocytes T CD8+ décroît de manière progressive et irréversible, ce qui aboutit à la formation d’une population de lymphocytes T CD8+/CD28− qui possède une capacité de prolifération beaucoup plus faible dans des conditions de culture standards. De manière parallèle, ces lymphocytes acquièrent à leur surface l’expression du CD57 [9], [16] and [17](figures 1B et 2). Ils perdent également progressivement l’expression de l’antigène CD27, traduisant l’état de différenciation avancé de ces lymphocytes. Enfin, ils expriment plus fréquemment l’antigène CD45RA que l’antigène CD45RO et ont

une faible expression de l’antigène CD62L, témoignant bien du caractère « sénescent » de ces lymphocytes [7] and [9]. Ces observations suggèrent ainsi que la population CD28−/CD57+/CD27− dérive de cellules CD28+/CD57−/CD27+. Cette hypothèse est corroborée par la mise en évidence de séquences identiques de la région CDR3 entre ces deux populations lymphocytaires [18]. Les lymphocytes T Amylase CD8+/CD57+ correspondraient donc à des lymphocytes T mémoires/effecteurs activés, dans un état de différenciation terminale ayant le plus souvent perdu leur potentiel cytotoxique et réplicatif et ce, dans un contexte stimulation antigénique chronique [11] and [19]. Ces lymphocytes ont par ailleurs un raccourcissement significatif de la taille des télomères, qui témoigne d’un processus de sénescence tardive [20]. Ainsi, chez le sujet infecté par le VIH, ces lymphocytes produisent de l’interféron-γ ; cependant, en présence de molécules co-stimulatrices, ils se révèlent incapable de s’expandre en réponse aux peptides dont ils sont spécifiques.

For example, not only are sexuality and delinquency heritable

For example, not only are sexuality and delinquency heritable selleck inhibitor but genetically they go together. Among adolescents, 36–49% of the sexual intimacy engaged in by one sibling was predicted by the amount of delinquency engaged in by the other sibling (Rowe, Rodgers, Meseck-Bushey, & St. John, 1989). A subsequent study found that individuals with high scores on measures of

sexuality and delinquency correlated positively with measures of impulsivity, deceitfulness, and rebelliousness, and negatively with those of parental affection and encouragement of achievement (Rowe & Flannery, 1994). Race differences are found on the r–K continuum. Africans average toward the r end, devoting resources to mating effort and producing more children but providing less parental care. East Asians average toward the K end, producing fewer offspring but investing more resources in them. Europeans average intermediately. Another three-way race difference is two-egg twinning, which is more numerous in Africans than in Europeans or East Asians (i.e., 16, 8, and 4 per 1000 twin births, respectively). Another is that Blacks have the most testosterone ( Ellis & Nyborg, 1992), which helps to explain their higher levels of athletic ability ( Entine, 2000). Testosterone acts as a “master switch.” It

goes everywhere in the body and affects many bio-behavioral systems. buy BAY 80-6946 It affects self-concept, aggression, altruism, crime, and sexuality, not just in men, but in women too. Testosterone controls muscle mass and the deepening of the voice in the teenage years. It also explains why Black women have the most premenstrual syndrome (PMS) and East Asians the least. A path-breaking study by Templer and Arikawa (2006) analyzed data from 129 countries and found a remarkably high correlation of 0.92 between skin color and national L-NAME HCl IQ. Skin color was measured using data from

Biasutti (1967) estimated for the world’s indigenous people at the time of Columbus’s first voyage in 1492 and average national intelligence scores from Lynn and Vanhanen (2002). (Templer and Arikawa’s rationale for using the year 1492 to define skin color in indigenous populations came from the authoritative tome by Cavalli-Sforza, Menzoni, and Piazza (1994) which mapped human genetic diversity.) The relationship between skin color and national IQs replicated separately within the three continents showing the generality of the phenomena: −0.86 for Africa; −0.55 for Asia; and −0.63 for Europe. Templer and Arikawa conceptualized skin color as a multigenerational adaptation to the cold winters encountered as people migrated north “out of Africa” over the last 70,000 years. Templer (2008) added life history variables to the 2006 national IQs compiled by Lynn and Vanhanen (updated from 2002). Templer found that skin color correlated across the 129 nations with IQ (−0.91), birth rate (0.

, 2007) The aim of this study was to increase standardization an

, 2007). The aim of this study was to increase standardization and reproducibility of cryopreservation by developing strategies for complete avoidance of animal products. Here we investigated the possibility of substituting the standard, serum-based cryopreservation with a serum-free protocol using serum alternatives (BSA fraction V and HSA), towards a protein-free, chemically defined cryomedium. Pretested serum was used for thawing and ELISpot analysis of all samples, Selleckchem SCH772984 as recommended by standard protocols. DMSO is extensively used as a cryoprotectant because of its high membrane permeability (Wang

et al., 2007). Intracellular DMSO replaces the water shell in macromolecules, so that cells are able to survive intracellular ice crystallization (Lovelock, 1953b). However, high concentrations of permeating solutes can result in extensive initial dehydration followed by rehydration (Woods et al., 2004). The resultant cellular shrinking and swelling can cause damage and even cell death (Mazur and Schneider, 1986). Therefore, the aim of this study

also was to investigate the effects of a reduced DMSO concentration on the recovery and functionality of PBMC. The protein-free medium was used with a DMSO concentration of 10% and 5%. However, the viability and recovery values as well as CX-5461 chemical structure the specific T cell reactivity against CEF and CMV peptides were slightly decreased with the reduced DMSO concentration. Thus, a simple reduction of DMSO seems not to be possible, so next steps should involve extracellular cryoprotectants like trehalose or hydroxyethyl starch (HES) (Ehrhart et al., 2009). Sample quality has to be guaranteed during long-term

storage of cells for retrospective analysis. Previous studies have already demonstrated that T-cell subsets do not appear to be significantly altered by cryopreservation or storage for up to 12 months (Ludgate et al., 1983, Glassman and Christopher, 1984 and Prince and Lee, 1986). Our results also show that there were no significant differences in viability, recovery and specific Methocarbamol functionality after long-term storage compared to short-term results. In summary, we have demonstrated that viability and recovery values were high with all serum-free media used, with lowest results for the HSA-based and the protein-free medium with 5% DMSO. Functionality of PBMC also seemed to be affected by these media. The cryopreservation efficiency of two serum-free media, one based on BSA, the other even protein-free and fully chemically defined with 10% DMSO, was comparable to the FBS-medium during storage for a few weeks and for several months. Cryopreservation in these media resulted in high viability and recovery values after short- and long-term storage of PBMC. Also the specific functionality was maintained. The straightforward use of the protein-free, fully chemically defined cryoprotocol enables freezing of large quantities of cell samples for research applications with high standardization and reproducibility.

G0900785 and by the Royal Society through the Paul Instrument Fun

G0900785 and by the Royal Society through the Paul Instrument Fund. The authors would

like to express appreciation to Clive Dixon, Mike Olsen, Ian Taylor, and Ian Thexton for fabrication of specialized glassware and equipment used in this work. The authors would like to also thank Prof. Ian Hall, and Prof. Peter Morris for useful discussions. A special thanks goes to Clémentine Lesbats for her assistance during the experiments. “
“By producing nuclear spin polarization far beyond that available at thermal equilibrium, hyperpolarization can provide improved sensitivity for NMR, enabling the detection of less concentrated molecules. In the area of molecular imaging, MRI has recently been used to study the distribution [1] and metabolism [2], click here [3] and [4] of hyperpolarized substrates. For instance, multiple studies have reported on the conversion of hyperpolarized 13C-labeled pyruvate to its metabolic

products, alanine, lactate and carbonate in vivo [2], [3], [4], [5] and [6], in which higher lactate production is an important indicator of cancer. This technique is already being translated to the clinic and a first trial is ongoing [7]. Major hyperpolarization techniques include dynamic nuclear polarization (DNP) [8] and [9], spin exchange optical pumping polarization of noble gases [10] and parahydrogen induced polarization (PHIP) [11], [12], [13], [14], [15] and [16]. Parahydrogen is a spin isomer of hydrogen with an antisymmetric singlet spin state. By incorporating this pure spin state into a molecule through a hydrogenation reaction, find more large signal enhancements have been observed in a variety of situations as first conceived by Bowers

and Weitekamp [12] and Pravica and Weitekamp [14]. In 2009, Duckett’s group developed a parahydrogen polarization technique that works without the need for the chemical modification of the substrate [17]. In this approach, Histone demethylase the substrate and the parahydrogen bind to a catalyzing metal complex simultaneously, thus enabling polarization to be transferred to the substrate through the scalar coupling network. The polarized substrate is subsequently released, and replaced by new substrate which is polarized in turn. Such Signal Amplification By Reversible Exchange (SABRE) has already been applied to detect trace amounts of chemicals [18], [19] and [20] and used in conjunction with zero-field NMR spectroscopy [21]. According to a theoretical description of SABRE, the signal enhancement level depends on the binding kinetics and the magnetic field in which polarization transfer occurs [22]. In order to achieve better enhancement, new catalyst precursors have been developed to tune the binding kinetics. Enhancements can be boosted by using the bulky electron-donating phosphines of the Crabtree catalyst [23].

9%) and in those with adult affective symptoms (34 1%) than in th

9%) and in those with adult affective symptoms (34.1%) than in those without (28.2% and 28.4%, for adolescence and adulthood, respectively). The differences in prevalence were similar in both cases, with confidence intervals just including the null value of zero (Table 1). In women, adolescent emotional problems were associated with higher odds

of the metabolic syndrome (23.2% in those without emotional problems versus 31.7% in those with emotional problems: OR = 1.53, 95% CI: 1.04, 2.26) (top half of Table 2). There was a suggestion that the association may be weaker in men than women although Natural Product Library order the test for interaction did not reach conventional significance levels (p = 0.22, OR for interaction = 1.44, 95% CI: 0.80, 2.59). Using the continuous measure of adolescent emotional problems the same association was observed in women (OR = 1.32 per one score increase, 95% CI: 1.00, 1.75), but not in men (OR = 1.12, 95% CI: 0.87, 1.46). Similarly, a higher risk of the metabolic syndrome was observed in women with affective symptoms learn more at age 36 years than in those without (23.9% without affective symptoms versus 32.6% with affective

symptoms: OR = 1.54, 95% CI: 0.97, 2.46) (bottom half of Table 2). However, there was no evidence of a statistical difference in the association between men and women (p for sex interaction = 0.53; OR = 1.29, 95% CI: 0.59, 2.83). Adolescent emotional problems were associated with high HbA1c level in the total sample (OR = 1.46, 95% CI: 1.11, 1.93) (top half of Table 1). Adult affective symptoms showed the strongest relationship with high triglyceride levels (bottom half of Table 1). For women, the associations between adolescent

emotional problems and all components of the metabolic syndrome, except HDL cholesterol, are in the same direction (Table 2). Similar consistency in the direction of most associations is also seen for adult affective symptoms. For men, the direction and size of associations are varied. In men, childhood emotional problems are only associated with raised Hba1c, and adult affective problems are strongly associated with hypertension (OR = 2.62, 95% CI 1.03–6.69). This association was not observed in women (OR = 1.01, 95% CI 0.68–1.51) and Histamine H2 receptor there was evidence of a sex difference in this relationship (p for sex interaction = 0.07; OR = 0.39, 95% CI: 0.14, 1.07) (bottom half of Table 2). Analyses including both adolescent emotional problems and adult affective symptoms as predictors of metabolic syndrome in women result in slight decreases in both ORs when compared with the unadjusted estimates. Confidence intervals for both variables, however, now include 1 suggesting that these measures may not operate independently (adolescent emotional problems: OR = 1.46, 95% CI: 0.97, 2.18; adult affective symptoms: OR = 1.52, 95% CI: 0.93, 2.47).

2 min, forming a pin-point colony (PC) only after two days incuba

2 min, forming a pin-point colony (PC) only after two days incubation on a drug-free agar plate. The PA pattern of 6R-P is shown in Fig. 4. In contrast to Mu50, 6R-P does not form colonies

on the agar plates containing 7 mg/L or greater concentrations of vancomycin within 48 h incubation, whereas, it does after 72 h–144 h of incubation (Fig. 4). The most striking feature of 6R-P is the instability Pictilisib ic50 of VISA phenotype. When passaged on drug-free agar plates, it generated phenotypic revertants (PR) having larger colony sizes and significantly decreased vancomycin resistance. When 6R-P was passaged in drug-free medium, the culture was quickly overgrown by PR cells within several days. The appearance rate of PRs from 6R-P was around 1 × 10−6 and was comparable to that of the emergence rate of VISA from hVISA [52]. A total of 25 sVISA strains were obtained from Mu3 by selection with 6 mg/L of vancomycin [66]. The colonies that appeared on the vancmycin plates after 72 h (3 days) to 144 h (6 days) incubation at 37 °C were picked, colony-purified, and established as sVISA strains. Their vancomycin MICs increased with time

of incubation, while that of clinical VISA strains, represented by Mu50, did not [66]. Some sVISA strains reached to the MIC values of 24 mg/L to 32 mg/L after 48–96 h incubation, whereas Mu50 remained at MIC of 12 mg/L throughout the incubation time up to 144 h [66]. This high MIC values of sVISA strains, however, were I-BET-762 molecular weight very unstable, and PRs with large colony size, and decreased vancomycin resistance

appeared quickly in the drug-free culture. Some sVISA strains are much more unstable than 6R-P, and generated large colonies with reduced vancomycin resistance even within 72 h of incubation (Fig. 5). The biological feature of sVISA is intriguing. The sVISA status is easily acquired by SPTLC1 hVISA, and even by VSSA [66]. The sVISA phenotype is a transient phenotype, but it can be maintained stably as long as it is passaged on the vancomycin-containing agar plates. Thus, sVISA phenotype is likely to be maintained as long as vancomycin therapy continues. When vancomycin treatment is lifted, sVISA would quickly revert to hVISA without leaving the evidence of VISA infection. This transient nature of resistance of sVISA may explain at least a part of lower rate of VISA isolation than the occurrence rate of the vancomycin-refractory MRSA infection. 4) RNAP regulatory mutation is a frequent mechanism for VISA phenotype RNAP mutation has been recognized as one of the major genetic events raising VISA [33]. It was the case for sVISA as well. The whole genome sequence determination of 6R-P revealed a single mutation in rpoB gene encoding β subunit of RNAP [66]. The identified mutation rpoB(R512P) was introduced into a VSSA laboratory strain ΔIP by an allelic replacement method [66].

Os estudos têm revelado eficácia clínica e histológica31 No enta

Os estudos têm revelado eficácia clínica e histológica31. No entanto ainda são necessários mais ensaios clínicos que aprovem o seu uso na prática clínica5.

A dilatação esofágica está indicada quando surgem sintomas secundários à estenose esofágica, causando disfagia e impacto alimentar. No entanto, está associada ao risco de hemorragia, perfuração e dor torácica5. Nas estenoses menos graves pode, inicialmente, tentar-se uma dieta de evicção ou terapêutica farmacológica antes de um procedimento mais Lumacaftor cell line invasivo. No caso de estenoses cerradas deve proceder-se de imediato à dilatação4. A figura 1 resume a abordagem clínica, diagnóstica e terapêutica no caso de suspeita de EEo. Relativamente ao seguimento dos doentes com EEo, não existe um consenso. Alguns autores defendem a realização periódica de EDA com biópsias enquanto outros sugerem o estudo histológico apenas se ocorrer alteração nos sintomas, adesão à terapêutica ou, se for necessário,

tomar decisões terapêuticas5 and 25. A primeira EDA com biópsias deve ser realizada no mínimo 4 a 8 semanas após inicio da terapêutica5. A esofagite eosinofílica é uma patologia emergente, atualmente selleck chemicals llc com critérios de diagnóstico bem definidos. No entanto, a sua história natural, o tratamento a longo prazo e a monitorização destes doentes ainda não estão bem definidos. O diagnóstico precoce exige um elevado índice de suspeição e é fundamental para prevenir potenciais complicações. As respostas alérgicas parecem ter

um papel fulcral na etiopatogenia desta doença e a avaliação alergológica tem assumido um papel cada vez mais importante na abordagem diagnóstica e terapêutica destes doentes. Deste modo, a avaliação otimizada da EEo requer uma equipa médica multidisciplinar, incluindo gastrenterologistas e imunoalergologistas. Os autores declaram não haver conflito de interesses. “
“The development of pancreatic collections may occur in different clinical set-ups. The most frequent causes are acute or chronic pancreatitis, neoplasms, surgery or trauma.1, 2 and 3 In recent years, ERCP has become an important cause of acute pancreatitis as well, possibly leading to pancreatic collections in more severe cases.2 and 4 Pancreatic necrosis, which is defined as diffuse Sulfite dehydrogenase or focal areas of nonviable pancreatic parenchyma, develops in nearly 20% of patients and is accompanied with a mortality rate varying from 8 to 39%.5 and 6 Since 1992, peripancreatic fluid collections have been classified according to the Atlanta Criteria in order to decrease erroneous interpretations previously made.1, 3 and 6 Additionally and for more practical purposes, pancreatic fluid collections may also be subdivided into three groups: (a) acute pancreatic-fluid collections; (b) pseudocysts; and (c) walled off pancreatic necrosis (WOPN).

e SMHI (Sweden), FMI (Finland), DMI (Denmark), BSH (Germany), EM

e. SMHI (Sweden), FMI (Finland), DMI (Denmark), BSH (Germany), EMHI (Estonia), LHMT (Lithuania) and IMGW (Poland). The sea levels from Germany, Denmark, Poland, Lithuania and Estonia are adjusted to the zero reference tide gauge of the water-level indicator of NAP (Normaal Amsterdams Peil) using the transformations

of the national reference systems (Coordinate Reference Systems), so as to comply with the standards of the European Vertical Reference System (EVRS 2000) (http://www.crs-geo.eu/crseu/). STA-9090 Sea level data are converted to an accuracy of 1 cm. Swedish and Finnish sea level data do not have a general water level ‘zero’ owing to the rapid uplifting of their lands with different velocities. The values here are given relative to the mean water levels for each station. The probability of occurrence of theoretical sea levels for several tide gauge stations from different coasts of the Baltic Sea is also determined in this work (section 3.2). These analyses use the maximum and minimum annual sea levels from the period 1960–2010. The

Gumbel distribution and the maximum likelihood method were used to determine the maximum theoretical level of Pexidartinib purchase a hundred-year water level (the hundred-year return period). The probability density function of the Gumbel distribution is based on statistical distributions of extreme values that occur in regular subperiods of the series. For instance, it can describe the distribution of the annual sea level maxima considered in this paper. The probability density function of the Gumbel distribution

is doubly exponential and described by the formula (Gumbel 1958) equation(1) fx=1a^e−x−b^a^−e−x−b^a, where Aldehyde dehydrogenase a^ – scale parameter (determining the dispersion of the distribution along the x-axis), b^ – location parameter (determining the location of the distribution along the x-axis), e – the base of the natural logarithm. The idea of relating the statistical distribution to observational data is to determine the distribution parameters a^ and b^ by means of the maximum likelihood method. The Pearson type III distribution, the usual one in hydrology (Kaczmarek 1970), was used to determine the theoretical, minimum sea levels equation(2) fx=αλΓλe−αx−ϵx−ϵλ−1, where α, ∊ ε, λ – the distribution parameters which should meet the following requirements: x ≥ ∊ (lower limit of the distribution), α > 0, λ > 0; Γ(λ) – gamma function of the variable λ. The parameters of the Pearson type III distribution were also assessed by means of the maximum likelihood method. This work studies the consistency of the accepted theoretical distribution with the empirical distribution (with the series of sea level observations) by means of the Kolmogorov test of normality. All the calculations were done with Matlab.

The top elevation of the uppermost layer represents the land surf

The top elevation of the uppermost layer represents the land surface and was approximated using an imported GSK-J4 and resampled digital elevation model. The bottom elevation of the fifth layer represents the bedrock surface, thereby constraining flow within the valley fill thickness ranging between 3 and 120 m thick. The bedrock surface was interpolated from available well logs, both in published literature (Randall, 1972) and public records from NYSDEC. The first upper two layers of the model represent the unconfined aquifer system. The third layer is a clay unit, which serves to confine the lowest two layers. The thickness and elevation

of the third layer was also interpolated from well logs (Randall, 1972). Both aquifer systems – upper and lower – were split into two layers apiece, with their interlayer elevation set at half of the aquifer thickness in each cell. There are four hydraulic conductivity units in this model (Fig. 4). The uplands are considered one homogeneous, low-conductivity unit, primarily serving as a transmitting media between the external boundary conditions and the valley walls. Separate hydraulic conductivity units were assigned to

the upper and lower aquifer systems. Cells representing the clay confining unit were assigned to the fourth conductivity DNA Damage inhibitor field. Any cell in the third layer with a thickness greater than 3 m is considered part of the confining unit. The remainder of the third layer, where the confining unit is thin or absent, is part of Dipeptidyl peptidase the upper aquifer hydraulic conductivity unit. Manual calibration indicated that this model was not significantly sensitive to conductivity of the confining unit in layer three at

the regional scale. Although there is extensive heterogeneity within the valley drift sequences, it is difficult to capture such a variability at this scale. Therefore, these hydraulic conductivity values better represent regional, effective conductivity. Uniform recharge of 62 mm/year was applied to the top of the model, representing the component of groundwater recharge derived from the infiltration of precipitation falling directly in the valleys. This value was approximated by adding the total volume removed from the system (through municipal pumping) to the net regional recharge estimated from the analytic element model (Best, 2013). Constant head boundaries on the outside of the active model area provide the lateral aquifer recharge derived from overland runoff, tributary infiltration, and interflow. In the baseline model, the constant head contribution to groundwater inflow from the boundary of the model was approximately 42%. Constant head contributions in the withdrawal scenarios were evaluated to ensure that this fraction of groundwater input did not unrealistically increase, results of which will be discussed in the sensitivity analysis. The Streamflow-Routing Package (Prudic et al.

Those who failed to match all stimuli were excluded from the stud

Those who failed to match all stimuli were excluded from the study (2 7-year-olds). Reading fluency for experimental Alectinib order words was measured outside the scanner in a self-paced reading-words-aloud task. Reading accuracy and the time from word presentation to next word-initiating button press were recorded. In the scanner, children received movement reduction training whilst watching a funny cartoon. The cartoon was paused when

an MR-compatible video camera recorded excessive movement. This training continued until the participant was lying sufficiently still for several minutes. During the fMRI experiment, participants performed a one-back categorisation task; they pressed a button with their right index finger when the same animal or tool picture (e.g., white cat, black cat) or the same animal or tool word (e.g., CAT, cat) was presented twice PTC124 manufacturer in a row. Each trial

began with a 1.5 s stimulus followed by a 0.8 s fixation screen. With this presentation duration, it is highly unlikely that subjects of any age failed to process word content, since from age 7 years onwards, semantic priming effects occur for briefly presented words (Chapman et al., 1994 and Plaut and Booth, 2000), even when word primes are task irrelevant (Simpson and Foster, 1986 and Simpson and Lorsbach, 1983) or ignored (Ehri, 1976 and Rosinski et al., 1975). Responses were recorded with a Lumitouch button box. Participants were instructed to fixate a central cross at all times, except during word blocks, when the cross was not present. There were 4 runs of 6 min 42 s. Each run consisted of 5 animal picture blocks, 5 tool picture blocks, 5 animal word blocks, 5 tool word blocks and 5 fixation baseline blocks of 16.1 s each (7 trials). Block and stimulus order were randomised with no stimulus repetitions within blocks. Target trials occurred 12 times during each run

– 3 times for each stimulus category. see more Button-press-related motor activation in the brain should not affect any contrasts of interest because (a) responses were infrequent, and (b) matched across conditions. To keep participants motivated, hits and false alarms were shown after each run. After fMRI, children’s reading abilities were measured using the Sight Word Efficiency Subtest of the TOWRE (Torgesen, Wagner, & Rashotte, 1999), a standardized test of reading accuracy and efficiency for pronouncing printed words. Raw scores reflect the number of words on a list that are read accurately within 45 s. MR data were collected with a Siemens TIM Avanto 1.5T scanner, using a 32-channel receive-only head coil. Data from 5 adults was collected without the front part of the coil (leaving 2/3 of the channels). Because this only leads to a lower signal to noise ratio in the orbitofrontal regions it did not affect any regions where an effect was expected, and so the data of these participants was included in the analysis.