P27 THE IMPACT OF HEALTH BELIEFS ON OSTEOPOROSIS TREATMENT Debora

P27 THE IMPACT OF HEALTH BELIEFS ON OSTEOPOROSIS TREATMENT Deborah T. Gold, PhD, Duke University Medical School, Durham, NC; Andrew Calderon, BS, Osteoporosis Medical Center, Los Angeles, CA; Stuart L. Silverman, MD, Cedars Sinai, Los Angeles, CA INTRODUCTION The Health Belief Model helps explain which patients are screened, evaluated or treated

for osteoporosis (OP) (Nadler Mdivi1 manufacturer et al., 2013). Furthermore health beliefs may be an important factor in compliance and persistence with OP medications (Schousboe, 2013). Health beliefs include beliefs about OP medication (risks and benefits) and beliefs about medical care (prefer to self treat vs. prefer to take medication). Little empirical research has been done to understand what factors are important in the learn more development of health beliefs of postmenopausal (PM) women making decisions about their bone health. In analyses reported here, we hypothesized that important factors in development of these health beliefs include race/ethnicity, age, education, SES, and history of prior fracture. MATERIAL AND METHODS: As part of a study of racial/ethnic differences in patient Temsirolimus clinical trial preferences for OP medication, we collected information about OP health and treatment beliefs and medication care preferences

in 367 PM women at risk of OP fractures (mean age = 76.7, (SD = 7.1); n = 100 Caucasian, n = 82 Asian, n = 85 Hispanic; n = 100 African Etomidate American). Health beliefs were measured with the Osteoporosis Health Beliefs Scale (Cadarette et al., 2009) and health care preferences were measured using the Medical Care Preferences Scale (Ganther et al., 2001). The health beliefs scale assesses perceived benefits and risks of OP treatment while the preferences scale measures personal preferences along a continuum anchored by self-treatment on one end versus external care seeking on the other. RESULTS: We found no statistically significant differences in beliefs across race/ethnicity with either the health belief scale or the medical care preference scale. However, both scales revealed statistically significant

differences based on social characteristics including age, with sixth decade women more likely to consider OP treatment (p = 0.039) than older women, and education, where women with less education were more likely to self treat (p = 0.01) and less likely to consider OP medication (p < 0.001) than those with more education. Patients with prior fracture(s) were more likely to consider OP treatment (p = 0.04), but prior fractures had no impact on the medical preferences scale. Individuals with lower SES were more likely to self treat (p < 0.0001) according to the preferences scale; however, SES had no effect on health beliefs about osteoporosis treatment. CONCLUSIONS: The data reported here suggest that health beliefs about OP are influenced by age, SES, education and history of prior fracture, although not by race/ethnicity.

The scanning probe unit scanned the entire tumors

The scanning probe unit scanned the entire tumors Belinostat supplier in several scanning paths with a vertical interval of 0.1 mm. Thus, a selleck chemicals llc magnetic image for the tumor could be constructed, as shown in Figure  2a. SPIONPs under AC field excitation generally expressed the characteristics of AC susceptibility. Therefore, the SSB signal from the in-phase component of the AC susceptibility of SPIONPs was in proportion to the SPIONP concentration [16]. The

3-T MRI (Bruker Biospec System, Karlsruhe, Germany) and a volume coil were used for T2-weighted images. In parallel with the arrangement of the anesthetized mouse, a long tube filled with deionized (DI) water was inserted as the intensity reference to dismiss the instrument drift at various times. AZD2014 Producing the coronal images of each entire mice body at 2-mm intervals required nearly 2 h. In general, the uniformity of the static field and gradient field is distorted by SPIONPs, resulting in the dephasing of the proton nuclear spin and, subsequently, the reduction of nuclear magnetic resonance (NMR) intensity induced by the pulse field of MRI [20]. Hence, the labeled tumor cells using bound SPIONPs expressed a darker image. Therefore, SPIONPs were the contrast agent of the MR images. For ICP examination (EVISA Instruments, PE-SCIEX ELAN 6100 DRC,

High Valued Instrument Center, National Science Council, Kaohsiung, Taiwan), two pieces of tumor tissue from one euthanized mouse were both weighted by a 0.1-g weight

and then dissolved entirely in a HNO3 solution at a concentration of 65%; they were then diluted and examined. To evaluate the incorporation of an anti-CEA SPIONP quantity into the tumor tissue, the difference of Fe concentration between the varied post-injection and pre-injection times at the 0th hour was expressed as ΔC Fe (ppm). The tissue staining was processed (Laboratory Animal Center, National Taiwan University, Taipei, Taiwan), and the × 400 magnification of the optical images was observed using a light microscope. Pyruvate dehydrogenase HE staining, PB staining, anti-CEA staining, and CD 31 staining were performed to identify the tumor tissue, Fe element distribution, and anti-CEA SPIONP distribution; and the degree of tumor angiogenesis was related to the transportation of anti-CEA SPIONPs. Results and discussion Figure  1b shows the curve of the magnetism-applied field (M-H) curve of anti-CEA SPIONPs. Based on the ultralow hysteresis in the M-H curve, the anti-CEA SPIONPs expressed superparamagnetic characteristics. Furthermore, the X-ray pattern of the anti-CEA SPIONPs in Figure  1c depicts the crystal structure of anti-CEA SPIONPs obtained by X-ray diffraction. The major peaks correspond with the standard X-ray pattern of Fe3O4 (JCPDS card no. 65–3107), verifying that the magnetic material was Fe3O4, a magnetic iron oxide (IO).

94 95% CI 0 87–1 02) Levels on floor-to-waist lift was not relate

94 95% CI 0.87–1.02) Levels on floor-to-waist lift was not related SRTW (OR = 0.92 95% CI 0.62–1.38) Pass floor-to-waist lift was not related to SRTW (OR = 1.19 95% CI 0.46–3.05) No Gross and Battié (2005) Canada Prospective cohort 12 months N = 130 claimants with low back pain, mean age = 42 years (SD 11), 82 men and 48 women Care provided at the Workers’ Compensation Board-Alberta rehabilitation facility Isernhagen Work

System FCE Work-related recovery expectations, Organizational policies and practices, Injury duration at time of FCE Days until suspension of time-loss benefits Fewer failed tasks (HRR = 0.91 95% CI 0.87–0.96) and higher floor-to-waist lift (HRR = 1.55 95% CI 1.28–1.89) were associated with faster suspension of benefits Yes Claim find more closure Fewer failed tasks (HRR = 0.93 95% CI 0.89–0.98) ARN-509 and higher floor-to-waist lift (HRR = 1.42 95% CI 1.12–1.80) were associated with faster claim closure Yes Sustained return-to-work (SRTW) Fewer failed tasks (OR = 0.95 95% CI 0.89–1.03) and higher floor-to-waist lift Foretinib research buy (OR = 0.91 95% CI 0.63–1.33)

were not significantly associated with future SRTW No Gross and Battié (2006) Canada Prospective cohort 12 months N = 336 claimants with upper extremity disorders, mean age = 45 years (SD 11), 239 men and 97 women Care provided at the major Workers’ Compensation Board-Alberta outpatient rehabilitation facility Isernhagen Work System FCE Age, Gender, Employment status, Days between FCE and time to total temporary disability suspension and time to claim closure, Days from injury to FCE, Pain score on disability index, Pain Visual Amobarbital Analog Scale, Clinician recommendation regarding fitness or readiness to work following FCE administration, Job physical demands, Pre-injury annual salary, Number of health care visits for the compensable condition, Total number of previous claims, Number of previous

upper extremity claims Days until suspension of time-loss benefits Higher weight lifted on the waist-to-overhead lift (HRR = 1.51 95% CI 1.29–1.87) and on floor-to-waist lift (HRR = 1.21 95% CI 1.06–1.38) were associated with faster suspension of benefits Yes Claim closure Higher weight lifted on the waist-to-overhead lift (HRR = 1.81 95% CI 1.49–2.20) and on the floor-to-waist lift (HRR = 1.29 95% CI 1.13–1.49) were associated with faster claim closure Yes Sustained return-to-work (SRTW) Waist-to-overhead lift OR = 0.87 95% CI 0.60–1.27) and floor-to-waist lift (OR = 1.05 95% CI 0.70–1.17) were not associated with future SRTW No Streibelt et al.

It was suggested, “”that plant sugars or sugar alcohols may const

It was suggested, “”that plant sugars or sugar alcohols may constitute signals that facilitate adaptation of certain fungi to a specific host plant”". Some of such compounds are differentially utilizable by Microdochium spp. Another study reported that Neotyphodium endophytes were inhibited in vitro by high concentrations of hexose and were incapable of utilizing xylose and arabinose [51]. These findings were supported by results showing that Neotyphodium lolii grows more slowly in varieties of its host Lolium perenne bred for intrinsically

high sugar concentrations [52]. For AM fungi, it was suggested that competition for the same carbon sources present in the same niche caused LCZ696 solubility dmso differential colonization [53]. A report comparing ericoid and orchid mycorrhizal fungi found that carbon source utilization Erastin molecular weight was generally quite similar in vitro except for distinct differences for tannic acid and certain amino acids [54]. These publications indicate that the quality and the quantity of buy YAP-TEAD Inhibitor 1 carbon sources available in the host may be one of the attributes influencing the composition of the associated fungal community. Although the BIOLOG system provides interesting insights in the capacity of fungi to utilize various carbon sources, the difference in growth conditions in vitro compared to in planta should be considered. Single carbon sources

are tested in vitro, whereas in planta many different sources are present. For the moment, it is not clear whether the carbon sources differentially used by Microdochium spp. in vitro are available

at contrasting levels in roots or whether they have physiological importance for the fungi. Furthermore, competition with other endophytes for carbon sources may also influence their occurrences in the field. Thus, the challenging Immune system task remains to prove that differential utilization of carbon sources in vitro contributes to the coexistence of endophytes in planta. Interactions between species implied by positive or negative co-occurrence was the third factor examined with respect to the differential colonization of the roots of common reed by Microdochium spp. Although spatial niche partitioning between M. bolleyi and M. phragmitis was significant, it was not perfect. Since none of the comparisons assessed by Fisher’s Exact test exhibited any negative co-occurrence, a direct antagonism between these two species is unlikely. Moreover, in 8.4% of the samples both species were detected which may suggest “”true”" coexistence. Otherwise, reduced competition for space or carbon (or other essential compounds and ions) may explain this finding. This could occur if colony sizes were much smaller than sample sizes or if the two species used different resources. However, the two Microdochium species constitute only a small part of the entire fungal community colonizing common reed. Thus, antagonism or synergism might be indicated when considering additional fungi.

In comparison to bacterial alginate, algal alginate showed a mino

In comparison to bacterial alginate, algal alginate showed a minor binding capaticity. However,

binding of lipase to algal alginate was reported previously [34]. In contrast to bacterial alginate Entospletinib price of P. aeruginosa, the algal alginate lacks O-acetyl groups and comprises a different monomer sequence which is characterized by the presence of guluronic acid rich regions (G-blocks) [22, 49]. Since other studies did not reveal an influence of the O-acetyl groups on the binding of lipases [33] the here observed effect might be based on the different monomer structure of algal and bacterial alginates. It was shown that within the G-blocks of algal alginates specific intra- and intermolecular structures were formed (egg box). Within the egg boxes negative charges of the alginate molecules are directed to each other and are complexed via divalent cations.

Thereby, the negative charges were shielded [50]. Figure Evofosfamide clinical trial 2 Binding of purified lipase LipA from P. aeruginosa to polysaccharides. Purified lipase LipA (36 ng/ml) from P. aeruginosa was incubated at 30°C in microtiter plates in the absence (−○-) and in the presence of immobilized polysaccharide films of (−■-) bacterial alginate from P. aeruginosa SG81 shown in red, (−▲-) xanthan shown in green, (−Δ-) algal alginate shown in pink, (−□-) levan shown in bright blue and (−●-) dextran shown in dark blue. Represented are carbohydrate concentrations used for coating of the microtiter plate wells. The bound lipase was many detected by activity measurements using pNPP as substrate. Results are shown as mean of five independent experiments +/− standard deviations. Significance of differences in lipase binding between coated and uncoated wells was calculated by ANOVA for the highest tested polysaccharide concentration. *** p < 0.001; ** p < 0.01. In summary, the experiments suggest that the

binding of lipases to alginate depends on the negative charged monomers of the polysaccharide indicating ionic interactions between the molecules. Heat stabilization of lipases by polysaccharides To investigate the biological impact of the interaction between lipase and bacterial alginate, heat inactivation experiments were performed. Incubation of purified lipase for 20 min at different temperatures in the presence and absence of polysaccharides showed an obvious influence of alginate on the stability of the lipase activity (Table 2). Without heat treatment (37°C) lipase activity stayed constant over 20 min in the presence and absence of polysaccharides at ΔA401 = 0.66 +/− 0.15 corresponding to an activity of 2.3 +/− 0.5 nmol/min × μg AMN-107 solubility dmso protein. Furthermore, at temperatures up to 50°C the lipase seemed to be generally stable. The addition of polysaccharides only had a minor effect. At higher temperatures (> 80°C) the protective effect of polysaccharides was lost. However, at approximately 70°C a significantly increased temperature tolerance of the lipase was observed in the presence of bacterial alginate.

J Occup Rehabil 12(4):257–267CrossRef CNAMTS (2007) Résultats 200

J Occup Rehabil 12(4):257–267CrossRef CNAMTS (2007) Résultats 2004 des principeaux tableaux de maladies professionnelles. Database on the Internet. Available from: http://​www.​risquesprofessio​nnels.​ameli.​fr/​fr/​maladies_​professionnelles​_​2/​ [Updated: 25/03/2009—Source: CNAMTS] (cited: 28-07-2010) Cole DC, Hudak PL (1996) Prognosis AMN-107 price of nonspecific work-related musculoskeletal disorders of the neck and upper extremity. Am J Ind Med 29(6):657–668CrossRef De Boer AG, van Lanschot JJ, Stalmeier PF, van Sandick JW, Hulscher JB, de Haes JC, Sprangers

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seropedicae

SmR1 (GenBank: CP002039, [29]) as shown in Ad

seropedicae

SmR1 (GenBank: CP002039, [29]) as shown in Additional file 1, Figure S3. All of these putative S63845 order promoter regions, with the exception of phaP2, were assayed for DNA binding by His-PhbF. DNA band-shift assays showed that purified His-PhbF was able to bind specifically to these eleven promoter regions (Figure 1 and results not shown) but not to the unrelated nifB promoter [40](Additional file 1, Figure S4) indicating that the protein is active. The apparent dissociation constants observed varied from 150 nM (phaP1) to 450 nM (phbF). Figure 1 The DNA-binding assays of purified His-PhbF from H. seropedicae SmR1 to the promoter regions of phaP1, phbF, dskAphbC, fadBphbA, phbCphbB and H_sero3316phaB were performed as described in Material and Methods. DNA promoter regions used in the assays are indicated by vertical Dorsomorphin black arrow heads and numbers indicate base position related to the translation start of each gene. Panel A: DNA labeled with [32P]. Lanes 1 to 5 indicate increasing amounts

of purified His-PhbF (0, 280, 570, 860 or 1100 nM). Panel B: Fluorescent labeled DNA. Lanes 1 to 8 indicate increasing amounts of purified His-PhbF (0, 62, 125, 250, 500, 750, 1000 or 1250 nM). Protein concentrations were calculated assuming His-PhbF as a tetrameric protein. These twelve promoter regions (including phaP2, additional file 1, Figure S3) were also analyzed in silico using the MEME program [35] which indicated the sequence TG[N]TGC[N]3GCAA as a probable DNA-binding motif for PhbF (Figure 2A). A similar sequence (CTGC[N]3GCAG) Phosphatidylinositol diacylglycerol-lyase PLX 4720 was also described in R. sphaeroides FJ1 as the DNA-binding site for the regulator PhaR [41]. Both sequences show two highly conserved triplets (TGC and GCA) which seem to be essential for DNA-binding of R. sphaeroides PhaR [41]. Figure 2 Panel A: Sequence logo representing the consensus sequence of pha promoter

regions identified by the program MEME motif discovery tool. In the y axis the information is represented in bits indicating the nucleotide frequency in the sequence at that position. The putative consensus sequence probably recognized by PhbF is indicated. Panel B: DNase I-protection footprinting assay was carried out as described in Material and Methods. The non-coding strand of the phbF promoter was used as a probe. The assays were in the absence (lane 1) or presence 155 (lane 2) or 312 nM (lane 3) of the purified His-PhbF tetramer. Lane P indicates the undigested promoter region. The DNA sequencing reaction is indicated in lanes A, C, G, and T. The region showing protection from DNaseI digestion is indicated by **. The probable σ70 promoter is indicated by *. Numbers indicate base position corresponding to the translation start codon. To verify if the TG[N]TGC[N]3GCAA sequence is important for DNA-binding of H.

J Trauma Manag Outcomes 2009, 3:6 PubMedCrossRef 12 Croce MA, Be

J Trauma Manag Outcomes 2009, 3:6.PubMedCrossRef 12. Croce MA, Bee TK, Pritchard E, Miller PR, Fabian TC: Does optimal timing for spine fracture fixation exist? Ann see more Surg 2001,233(6):851–858.PubMedCrossRef 13. Rutges JP, Oner FC, Leenen LP: Timing of thoracic and lumbar fracture fixation in spinal injuries: a systematic review of neurological and clinical outcome. Eur Spine J 2007,16(5):579–587.PubMedCrossRef 14. Stahel PF, Smith WR, Moore EE: Current trends in resuscitation strategy

for the multiply injured patient. Injury 2009,40(Suppl 4):S27–35.PubMedCrossRef 15. Weckbach S, Flierl MA, Blei M, Burlew CC, Moore EE, Stahel PF: Survival following a vertical free fall from 300 feet: the crucial role of body position to impact surface. Scand J Trauma Resusc Emerg Med 2011, 19:63.PubMedCrossRef 16. Oda I, Abumi K, Lu D, Shono Y, Kaneda K: Biomechanical role of the posterior elements, costovertebral joints, and rib cage in the stability of the thoracic spine. Spine (Phila Pa 1976) 1996,21(12):1423–1429.CrossRef 17. Watkins

Rt, Watkins R, Williams L, Ahlbrand S, Garcia R, Karamanian A, Sharp L, Vo C, Hedman T: Stability provided by the sternum and rib cage in the thoracic spine. Spine (Phila Pa 1976) 2005,30(11):1283–1286.CrossRef 18. Berg EE: The sternal-rib complex. A possible fourth column in thoracic spine fractures. Spine (Phila Pa 1976) 1993,18(13):1916–1919.CrossRef 19. Denis F: The three column spine and its significance in the classification of acute thoracolumbar spinal injuries. Spine (Phila Pa 1976) 1983,8(8):817–831.CrossRef 20. Gottschalk HP, Browne RH, Starr AJ: Shoulder girdle: patterns of trauma and associated HKI-272 nmr injuries. J Orthop Trauma 2011,25(5):266–271.PubMedCrossRef 21. Demetriades D, Velmahos GC, Scalea TM, Jurkovich Urocanase GJ, Karmy-Jones R, Teixeira PG, Hemmila PG, O’Connor JV, McKenney MO, Moore

FA, et al.: Diagnosis and treatment of blunt thoracic aortic injuries: changing perspectives. J Trauma 2008,64(6):1415–1418.PubMedCrossRef 22. el-Khoury GY, Whitten CG: Trauma to the upper thoracic spine: anatomy, biomechanics, and unique imaging features. AJR Am J Roentgenol 1993,160(1):95–102.PubMed 23. Lund JM, Chojnowski A, Crawford R: Multiple thoracic spine wedge fractures with associated sternal fracture; an Selleck Crenigacestat unstable combination. Injury 2001,32(3):254–255.PubMedCrossRef 24. Elgafy H, Bellabarba C: Three-column ligamentous extension injury of the thoracic spine: a case report and review of the literature. Spine (Phila Pa 1976) 2007,32(25):E785–788.CrossRef 25. Gopalakrishnan KC: el Masri WS: Fractures of the sternum associated with spinal injury. J Bone Joint Surg Br 1986,68(2):178–181.PubMed 26. van Beek EJ, Been HD, Ponsen KK, Maas M: Upper thoracic spinal fractures in trauma patients – a diagnostic pitfall. Injury 2000,31(4):219–223.PubMedCrossRef 27. Stahel PF, Smith WR, Moore EE: Role of biological modifiers regulating the immune response after trauma.

(A) Frequency of each HB in the dataset of genomic var tags (B-C

(A) Frequency of each HB in the dataset of genomic var tags. (B-C) The pairwise similarity among sequence types, where types are defined by homology block composition: Acalabrutinib the number of HBs shared between any two sequences divided by the average number of HBs within a sequence for those two sequences. (B) Frequency distribution of pairwise HB similarities between sequences in the genomic dataset. The approximately normal distribution contrasts with the bimodal distribution that has been observed for other data, when pairwise similarity is defined by amino acid identity [29]. (C) Sequences are hierarchically ordered based on pairwise HB similarity using the average-linkage method as implemented

in SciPy. The distinction between sequence tags containing two cysteines (cys2) versus four (cys4) is very clear, reflecting that recombination occurs at a faster rate within, relative to between, the two groups. While the diversity

of HB-types is almost an order of magnitude less complex than the diversity of aa-types, the former is nevertheless Lazertinib in vivo considerable and potentially functionally informative (Figure  3). Thus, even though these HBs were designed with reference to the var diversity of only a few parasite genomes (i.e., those analyzed in [8]), most of the sequence variation present within this local population is captured by homology to HBs, and so it is reasonable to hypothesize that the HBs capture functional variation among DBLα tags in this population, at least with regard to phenotypes known to be mediated by the DBLα domain. For example, it seems reasonable that the unique aspects of the HB composition observed for rosetting associated var Diflunisal tags (Figure  1B; Additional file 1: Figure S2) may be of functional significance. Figure 3 Two HB subnetworks: associated with severe versus mild spectrum disease. HB networks reveal two discrete HB subsets—one being associated

with severe spectrum phenotypes (orange) and the other being associated with mild spectrum phenotypes (blue). (A) The network of significant positive linkage disequilibrium coefficients (D) among HBs in the genomic dataset, based on a one-tailed significance threshold of p ≤ .025, reveals two subnetworks of linked HBs. (B) The network of significant associations between HB expression rates and phenotypes (p ≤ 0.05) with nodes colored according to the subnetworks of A. The HBs in the orange subnetwork are AC220 in vitro generally associated with severe disease spectrum phenotypes, whereas those in the blue subnetwork are generally associated with mild. The lack of connectivity between the severe and mild spectrum phenotypes in A is highly significant: even just considering the nodes of degree 3 or less, p < 0.0001 for the fact that each HB in the network is associated with mild or severe spectrum phenotypes, but not both.

311 nm, c = 0 498 nm [23], C 13 = 99 GPa, and C 33 = 389 GPa for

311 nm, c = 0.498 nm [23], C 13 = 99 GPa, and C 33 = 389 GPa for AlN [24]; and a = 0.354 nm, c = 0.5706 nm

[23], C 13 = 121 GPa, and C 33 = 182 GPa for InN [25]. For In x Al1-x N ternary alloy, both lattice constants and Poisson’s ratio v(x) are obtained by linear interpolation from the values of binaries. As a result, it can be concluded that the molar fraction of InN on a biaxially strained In x Al1-x N film is the only possible solution between 0 and 1 for the following third-order equation which presents x as a function only of two variables. The In composition (x) is accordingly to be calculated as x = 0.57 ± 1% (TMIn/TMAl, approximately 1.29), 0.64 ± 1% (TMIn/TMAl, approximately 1.4), 0.71 ± 1% (TMIn/TMAl, approximately 1.51), and 0.80 ± 1% (TMIn/TMAl, Selleck EPZ015938 approximately 1.63) by Vegard’s law. The XRD pattern of an In content of <0.64 exhibits extremely weak and broad peaks, which indicates that the film is of poor quality due to structural defects. Also, the In0.64Al0.36 N film shows a polycrystalline structure, suggesting that the in-plane residual stress of the In0.64Al0.36 N film is almost relaxed after growth. At above x = 0.71, the pattern indicates that the InAlN films are preferentially oriented in the c-axis direction. In addition,

a weak shoulder peak (2θ, approximately 31.909°) was detected at the highest In content of approximately Avapritinib clinical trial 0.71, indicating an intermediate layer between the film and the Si substrate. As can be seen in Figure  2b, the lattice parameters for

c-axis and a-axis obtained from symmetric (0002) and asymmetric ( ) diffractions of InAlN increased with the increase of In content. The results agree with the theoretical calculations and report of Guo et al. [26]. Figure  2b shows the calculated lattice parameters of all In x Al1-x N films with various In compositions. Both c and a lattice parameters exhibit essentially a linear dependence on the In composition with very small deviations from Vegard’s law. In our results, the bowing parameters of δ a  = 0.0412 ± 0.0039 Å and δ c  = -0.060 ± 0.010 Å describe the deviations from Vegard’s rule. Therefore, the variation of the In x Al1-x N lattice parameters with In content x can be approximated as follows: where InN and AlN lattice parameters are based on a previous study (for InN, a = 3.538 Å and c = 5.706 Å [27]; Oxalosuccinic acid for AlN, a = 3.11 Å and c = 4.98 Å) [23]. The lattice parameter of the In0.57Al0.43 N film was calculated to be larger than the theoretical value, which may be caused by phase separation and/or lattice strain. The in-plane residual stress of all InAlN films is shown in the inset of Figure  2b. When the In content is high (>71%), small tensile intrinsic stresses are observed. It has been proposed that one CBL0137 price reason for the occurrence of tensile intrinsic stresses is the existence of numerous grain boundaries.