Fig. 3 Mean percentage of species found in a single subsamples, forest- or GDC-0068 mw habitat type relative to the total number of species found in the study region The Mantel test of Sørensen’s indices among taxonomic groups showed significant positive correlations for nearly all groups (lichens excluded) in the terrestrial habitat, whereas only very low correlations were found in the epiphytic habitat (Table 3). The only significant correlation of lichens was with epiphytic ferns. Table 3

Correlations (R values) between similarity matrices of Sørensen’s (Bray Curtis) index of epiphytic (E) and terrestrial (T) species compositions per plot between the four study groups check details   Lichens Liverworts Mosses E T E T E T Ferns 0.15* – 0.13* 0.25** 0.18** 0.37***

Lichens     −0.13 – −0.01 – Liverworts         0.12 0.50*** * P < 0.05, ** P < 0.01, *** P < 0.001 Discussion TGF-beta inhibitor Forest structure and microclimate have been identified as principal drivers of diversity of ferns, bryophytes and lichens in tropical forests (Richards 1984; Sipman and Harris 1989; Wolseley and Aguirre-Hudson 1997; Holz and Gradstein 2005; Sporn et al. 2009) For terrestrial ferns, in addition, soil characters play an important role (Kluge et al. 2006). This is the first study that compares patterns of alpha and beta diversity among mosses, liverworts, ferns, and lichens in a tropical montane forest. We also separated epiphytic and terrestrial assemblages as well as forests occurring on ridge and slope because of the different environmental conditions of these habitats. Alpha diversity The epiphytic habitat was significantly richer in species than the terrestrial habitat. The taxonomic groups varied in their occurrence in the different habitat types. Whereas mosses were most species-rich in the terrestrial habitat, liverworts, Metformin research buy ferns and lichens were most diverse in the epiphytic habitat. Slope forests were generally richer in species than ridges forests. We presume that this pattern is linked to differences in structure between the two forest types. Probably, the higher trees

in slope forests provide more varied and more favorable microhabitat conditions as well as more space for different species to coexist (Mandl et al. 2008), (unpubl.data). Overall, on average only 5% (±31% SD) of the variance in species richness of one taxonomic group could be predicted by species richness of another. Considering only the epiphytic habitat, this value increased to 15% (±20%). However, these mean values conceal a high level of variation. Patterns of alpha diversity were highly congruent for ferns, liverworts, and mosses in the epiphytic habitat (R² = 0.28–0.41), and for ferns and liverworts to a lesser degree in the terrestrial habitat (R² = 0.28). Thirty two percentage of variance in epiphytic species richness of a given group was explained by other taxa (lichens omitted).

25 N in a total volume of 300 μl. The DNA was kept at room temperature for 30 minutes and then transferred on to ice. The GS + nylon membrane of required size was cut and saturated in 0.4 M Tris-Cl, pH 7.5 for 15 min and the DNA were spotted on to the membrane with the help of mini-fold apparatus from Whatman, Germany. The blots were air dried and UV cross linked before hybridization. We used 4.5 kb rDNA fragment (EcoRI to Hind III site) from HMe region of EhR1 (rDNA plasmid in HM1:IMSS strain

of E.histolytica) as probe for detection of Entamoeba positive samples that include both E.histolytica Z-VAD-FMK purchase and E. dispar (Figure 1A) [17]. Figure 1 Screening of stool samples by Dot-Blot method. (A) Linear map of EhRI episome (24.5 kb) showing the position of HMe probe (4.5 kb in size) common for both E. histolytica and E. dispar), E – EcoR1 site and H- Hind III site; rDNA I and rDNA II represent two inverted repeats of transcription units with various restriction sites and repeats (B) Representative

figure of Dot-blot analysis of stool sample using HMe probe. Rows 1 to 6 (column A-D) represent spots of DNA from stool samples. About MCC950 cell line 20 ng of DNA was loaded on each spot in triplicate on nylon membrane. Row 7 was blank. Row 8 (column A) E. histolytica HM1: IMSS genomic DNA as positive control; (column B) E. dispar SAW760 genomic DNA as positive control; (column C) E.Coli DH5α as negative control; (column D) Plasmid with cloned HMe as positive control. All samples were loaded in triplicate. Experimental details are provided in material and methods. Genomic DNA extraction DNA was extracted from the Dot blot positive

samples. An aliquot of 200 mg stool sample was used for selleck chemical isolation using QIAamp mini stool kit (QIAGEN,Germany) as per manufacturer’s guidelines. While isolating DNA from the stool samples through the above kit, pGEMT-easy plasmid containg 240 bp fragment of glycoprotein B (gB) gene aminophylline of phocine virus (20 ng/200 μl of ASL buffer) was added in ASL buffer as internal control during the isolation of genomic DNA [18]. PCR analysis of Dot blot positive samples To differentiate Dot-blot positive samples into E. histolytica and E. dispar, primers were designed from EhSINE2 for E. histolytica and from 18 S and ITS2 region of rDNA circle for E. dispar respectively (Figure 2A & B). Primer sequences were as follows; Eh-F 5’-GTCAGAGACACCACATGAA-3’, Eh-R 5’-GAGACCCCTTAAAGAAAC -CC-3’ and Ed-F 5’-GAAGAAACATTGTTTCTAAATCCAA-3’ & Ed-R 5’-TTTATTAA CTC ACTTATA-3’ [19]. Figure 2 Screening of Stool samples by PCR. (A) Schematic representation of location of Entamoeba histolytica specific primer. BH16197 is Genbank accession number of Entamoeba histolytica SINE-2 (EhSINE2) element; (B) Schematic representation of location of Entamoeba dispar specific primer from rDNA molecule. 18 S, 5.8 S and 28 S are corresponding ribosomal gene sequences and ITS-1 and ITS-2 refers to internal transcribed spacer 1 and 2; (C) Detection of E.

Appl Phys Lett 2008,92(15):152114.CrossRef 14. Yeh PH, Chen Selleckchem CDK inhibitor LJ, Liu PT, Wang DY, Chang TC: Metal nanocrystals as charge storage nodes for check details nonvolatile memory devices. Electrochim Acta 2007,52(8):2920.CrossRef 15. Yeh PH, Yu CH, Chen LJ, Wu HH, Liu PT, Chang TC: Low-power memory device with NiSi 2 nanocrystals embedded in silicon dioxide layer. Appl Phys Lett 2005,87(19):193504.CrossRef 16. Chen SC, Chang TC, Liu PT, Wu YC, Lin PS, Tseng BH, Shy JH, Sze SM, Chang CY, Lien CH: A novel nanowire channel poly-Si TFT functioning as transistor and nonvolatile SONOS memory. IEEE Electron Device Lett 2007,28(9):1696. 17. Yang SQ, Wang Q,

Zhang MH, Long SB, Liu J, Liu M: Titanium tungsten nanocrystals embedded in SiO 2 /Al 2 O 3 gate dielectric stack for low-voltage operation in non-volatile memory. Nanotechnology 2010, 21:24201. 18. Zhen LJ, Guan WH, Shang LW, Liu M, Liu G: Organic thin film transistor memory with gold nanocrystals embedded in polyimide gate dielectric. J Phys D Appl Phys 2008, 41:135111.CrossRef 19. Tsai TM, Chang KC, Chang TC, Syu YE, Chuang SL, Chang GW, Liu GR, Chen MC, Huang HC, Liu SK, Tai YH, Gan DS, Yang YL, Young R406 TF, Tseng BH, Chen KH, Tsai MJ, Ye C, Wang H, Sze

SM: Bipolar resistive RAM characteristics induced by nickel incorporated into silicon oxide dielectrics for IC applications. IEEE Electron Device Lett 2012,33(12):1696.CrossRef 20. Tsai TM, Chang KC, Chang TC, Chang GW, Syu YE, Su YT, Liu GR, Liao KH, Chen MC, Huang HC, Tai YH, Gan DS, Sze SM: Origin of hopping conduction in Sn-doped silicon oxide RRAM with supercritical CO 2 fluid treatment. IEEE Electron Device Cyclooxygenase (COX) Lett 2012,33(12):1693.CrossRef 21. Guan WH, Long SB, Jia R, Liu M: Nonvolatile resistive switching memory utilizing gold nanocrystals embedded in zirconium oxide. Appl Phys Lett 2007, 91:062111.CrossRef 22. Guan WH, Long SB, Liu Q, Liu M, Wang W: Nonpolar nonvolatile resistive switching in Cu doped ZrO 2 . IEEE

Electron Device Lett 2008,29(5):434.CrossRef 23. Liu Q, Guan WH, Long SB, Jia R, Liu M, Chen JN: Resistive switching memory effect of ZrO 2 films with Zr + implanted. Appl Phys Lett 2008, 92:012117.CrossRef 24. Tsai TM, Chang KC, Zhang R, Chang TC, Lou JC, Chen JH, Young TF, Tseng BH, Shih CC, Pan YC, Chen MC, Pan JH, Syu YE, Sze SM: Performance and characteristics of double layer porous silicon oxide resistance random access memory. Appl Phys Lett 2013, 102:253509.CrossRef 25. Chang KC, Tsai TM, Chang TC, Wu HH, Chen JH, Syu YE, Chang GW, Chu TJ, Liu GR, Su YT, Chen MC, Pan JH, Chen JY, Tung CW, Huang HC, Tai YH, Gan DS, Sze SM: Characteristics and mechanisms of silicon oxide based resistance random access memory. IEEE Electron Device Lett 2013,34(3):399.CrossRef 26.

Ates et al. [68] compared the results of laparoscopic simple closure without omental patch with that of conventional open repair in patients with small perforated duodenal ulcer and prove that is was as safe and as effective. On the other hand, Turner et al. [69] reported that suture without an omental patch would result in a significantly higher mortality rate than with a patch. However, most cases in their series were perforated gastric ulcers instead of juxta-pyloric perforation. Finally, Lunevicius www.selleckchem.com/products/gw3965.html et al. [70] reviewed 13 prospective and 12 retrospective studies and concluded that repair method should best be judged

by the properties of the ulcer edge. In short, although it seems that no single method is considered being the standard, the literature showed that there were no differences between these two most common adopted procedures in terms of postoperative recovery and incidence of surgical complications. To summarize, laparoscopic simple closure alone without adding an omental patch is a safe procedure for juxtapyloric QNZ supplier perforation in low risk patients. In terms of leakage rate and surgical outcome, the manoeuver to cover an omental patch on the repaired PPU did not show any additional advantage [71]. We suggest that Laparoscopic sutureless repair may

be a viable option in presence of limited laparoscopic experience, only in presence of small size perforations (i.e. microscopic or <2 mm www.selleckchem.com/products/pf-03084014-pf-3084014.html perforations) without significant peritoneal contamination and for low risk patients. We recommend primary repair in case of perforated peptic ulcer larger than 5 mm and smaller than 2 cm (Additional file 3 : Video 3). We suggest routine use omental patch to further protect the suture line (see Additional file 3 : Inositol monophosphatase 1 Video 3). We recommend avoiding use of glue as only method of closure

of PPU. We suggest use of glue only as an adjunctive measure to protect suture line or the omental patch. We suggest avoiding use of glue because of increased costs and risks of complications if serious doubts exist on the efficacy of primary closure. We suggest conversion to open procedure if the primary repair is deemed to be done not efficaciously. Resectional surgery The resection surgery is a viable option for giant peptic ulcers, commonly defined as having a diameter greater than 2 cm. These lesions have a higher risk of perforation. In gastric lesions, although the risk of malignancy is less than historically predicted, the incidence is still around 10% [72, 73]. There are no specific surgical treatment recommendations since the site of perforation and the secondary effects on the surrounding anatomical structures must direct the necessary interventions. These patients are also frequently in septic shock upon presentation when the amount of peritoneal spillage is large. This factor alone should significantly influence the choice of operative intervention.

denitrificans 4 Kingella denitrificans (2) S; SI Neisseria bacilliformis Moraxella catarrhalis (1) S; SI M. nonliquefaciens Moraxella catarrhalis (2) S; SI M. osloensis Moraxella catarrhalis (1) S; SI Neisseria

elongata 4 Neisseria cinerea (1) S; SC N. cinerea 4 Neisseria elongata (1) S; SI Capnocytophaga canimorsus 4 Neisseria elongata (1) S; SI Capnocytophaga gingivalis 4 Neisseria elongata (1) S; SI Eikenella corrodens 4 Neisseria elongata (3) S; SC N. elongata 4 Neisseria elongata (4) S; SI N. weaveri Neisseria gonorrhoeae (1) S; SI Moraxella lacunata Neisseria sicca (1) S; SC LCZ696 chemical structure N. sicca 4 Neisseria sicca (2) S; SI N. subflava Neisseria elongata (1) S; SI N. zoodegmatis Suttonella indologenes (1) S; SI Aggregatibacter actinomycetemcomitans 4 Not identified (1) N Aggregatibacter aphrophilus 4 Not identified (1) https://www.selleckchem.com/products/mk-5108-vx-689.html N Moraxella atlantae Not identified (1) N Moraxella canis Not identified (3) N Moraxella nonliquefaciens Not identified (2) N Moraxella osloensis Not identified (1) N Neisseria animaloris Not identified (3) N Neisseria elongata 4 Not identified (1) N Neisseria zoodegmatis Not identified (2) N Pasteurella bettyae Not identified (5) N Pasteurella multocida 6 Not identified (1) N Pasteurella stomatis 1 Final identification was assigned

using 16S rRNA gene identification as the reference method and if required with supplemental conventional tests. 2 Assignment to taxonomic level: S = species, G = genus, N = not identified. 3 Correctness of assignment: SC = correct at species level, SI = incorrect at species level, GC = correct at genus level, GI = incorrect at genus level, N = not identified. 4 Taxon included in the VITEK 2 NH database; Capnocytophaga spp. is included as genus. 5 Accepted as correct genus as Haemophilus aphrophilus was renamed as Aggregatibacter aphrophilus[22]. 6 Pasteurella multocida is included in the database of the VITEK 2 ID GNB card (bioMérieux). Discussion In this study, we analysed a large set of fastidious GNR Dynein clinical isolates covering diverse genera and species, which were obtained under routine conditions in a diagnostic microbiology laboratory. Molecular identification is vastly superior to conventional identification, both in

number of isolates assigned to correct taxon level and in accuracy (Table 2). A minority (6%) of the 158 isolates included in the study could not be assigned to species level by 16S rRNA gene sequence analysis. In contrast, 47% of the 158 isolates were not identified or misidentified by conventional Bcl-2 inhibitor phenotypic methods (Table 2). However, the performance of supplemental phenotypic tests was helpful to support the molecular identification in cases with low demarcation of two or more species due to highly similar 16S rRNA gene sequences (Table 1). Although the overall correct assignment to taxa by conventional phenotypic methods was rather poor, some species are easily assigned to correct species level by conventional identification procedures (Table 3).

AD has been VX-680 ic50 involved in drafting the manuscript and in measuring the CARS spectra. RK has been involved in drafting the manuscript. VF carried out the synthesis of the graphene nanoplatelets. OP carried out the synthesis of graphene oxide and participated in drafting the manuscript. All authors read and approved the final manuscript.”
“Background

Tin dioxide (SnO2) has drawn a great interest, among other oxides, related the response to oxidizing and reducing gases [1]. Microbiology inhibitor Nowadays the research is focusing on nanostructured materials, among other nanowires, because they have a large surface-to-volume ratio and show enhanced chemical stability and electrical performances [2, 3]. However, thin film technology is a core high-yield fabrication method for real-world sensors because of the main advantages such as low power consumption. In order to improve selectivity and sensitivity of the SnO2 thin films-based gas sensors, various dopants are used. It is well known that SnO2 thin film sensors doped with Ag additives

are very sensitive to low concentration of volatile sulfides such as H2S in air [4]. Up to now, this mechanism is not fully clear. However, it is certain that the influence of dopants like Ag must be related to the variation of the surface chemistry, morphology, and electronic properties of SnO2 thin films. Apart from the above, one of the most technologically relevant and still scarcely addressed problem in the world of real sensors is their degradation in time. This is why selleck the aging effect of SnO2 thin films after their air exposure related mainly to the undesired and uncontrolled C carbon

contamination coming from CO2 in the atmosphere is also of great importance [5]. This is even more serious when SnO2 nanostructures are covered with Ag additives. The aging problem in the case of pure SnO2 nanolayers prepared by laser-enhanced chemical vapor deposition (L-CVD) method has been already addressed in our recent studies [5, 6]. The main observation from Grape seed extract this study was that long-term exposure (aging) in dry air of L-CVD SnO2 thin films caused them to be covered with a large amount of undesired carbon species. They can be reduced after their ultrahigh vacuum (UHV) annealing up to 670 K. However, X-ray photoelectron spectroscopy (XPS) method cannot give any information concerning the forms of desorbing species. One can expect that this desorption process can be affected by the presence of Ag surface additives. This type of information can be obtained using, for instance, thermal desorption spectroscopy (TDS) method. This is why in this paper, we present the results of a comparative study of the surface chemistry and morphology of Ag-covered L-CVD SnO2 nanolayers carried out by XPS in combination with TDS, respectively.

Nature 2008,452(7190):975–978.CrossRef Competing interests The authors declare that they have no competing interests. Authors’ contributions AI wrote GDC-0994 mw the manuscript. HA and AI designed the experiment and analyzed the data with support from MT. HA acquired the ARPES data with support from AI, MA, and HN. High-quality single-crystalline samples were grown by MI, KF, SI, and SU. All authors discussed the results and commented on the manuscript.

All authors read and approved the final manuscript.”
“Background Among various oxide semiconductor photocatalysts, TiO2 has been studied extensively and considered to be the most appropriate for applications in the environmental field because of its biological and chemical inertness, cost effectiveness, strong oxidizing power, and long-term stability against chemical corrosion and photocorrosion [1]. The photocatalytic ability of TiO2 is strongly affected by morphologies, phase structures, macroscopic structures, and so on [2–10].

In addition, the surface property is a key factor influencing the photocatalytic activity [2]. The surface density for the 001 facets has been demonstrated to be higher than that for other facets with undercoordinated Ti atoms [11]. The exposed 001 facets of anatase TiO2 have been proven to possess high surface energy, which induces high reactivity [12, 13]. Therefore, photocatalysts with higher reactivity can be obtained by controlling the exposed crystal facets of TiO2[14]. Moreover, to improve the photocatalytic BX-795 in vitro activity of titania, reducing the band gap has been proven as a valid approach. An effective way to red shift the absorption edge can be achieved by doping one kind of element, such as F, Nb, and Mn [15–18]. After doping, Ti3+ states in TiO2 increase effectively. The existence of Ti3+ plays an important role on the enhancement of the photocatalytic activity [15]. Thus, the use of codoping by two or more elements is reported to result in a significant improvement for increasing the photocatalytic activity, such as Nb and N [19, 20], Zr and Y [21], and F, B, and Si [22]. In our previous work, titania micron

beads codoped with Nb and F were synthesized and used in DSSCs with beneficial result [23]. In this paper, the Nb, F-codoped TiO2 hollow spheres (NFTSs) were synthesized via a facile hydrothermal process using niobium oxide and hydrofluoric Gemcitabine supplier acid as codoping source. The phase structure, morphology, chemical composition, band gap energy, and photocatalytic activity of the obtained product were investigated. Methods Preparation of NFTSs All chemicals, including tetrabutyl titanate, niobium oxide (Nb2O5) powder, hydrofluoric acid, and lactic acid, were of analytical grade and used as received without further purification. Nb2O5 was dissolved using hydrofluoric acid to obtain a clear and transparent solution. The Ti precursor was prepared using tetrabutyl PF299 cost titanate chelated with lactic acid.

It has been demonstrated in a wide variety of bacteria that death and lysis of a subpopulation of cells can facilitate biofilm formation due to the release of DNA into the extracellular environment (eDNA) [17–22]. Likewise, cell death and lysis have been implicated in dispersal of cells from a mature biofilm [23–25]. In Staphylococcus

aureus, the Cid/Lrg system has been shown to be involved in the regulation of cell death, autolysis, and biofilm formation [17, 21, 26–28]. Characterization of S. aureus cid and lrg mutants has revealed that these operons have opposing effects on cell death and murein hydrolase activity [27, 29]. These observations, combined with the fact that LrgA and CidA share structural features with JQ-EZ-05 nmr the bacteriophage lambda family of holin proteins [29], have led to the hypothesis that CidA and LrgA control cell death and lysis in a manner analogous to effector and inhibitor holins, respectively [26, 30]. Bacteriophage holins are small membrane proteins that oligomerize Luminespib in vivo in the cell membrane, acting as “molecular clocks” that regulate the timing and lysis

of the host cell during lytic infection [31]. For example, the lambda S holin regulates cell death and lysis by the formation of large lipid-excluding “rafts” that promote cytosolic leakage as well as access of the phage-encoded endolysin (murein hydrolase) to the cell wall [32–34]. S. aureus CidA and LrgA have recently been shown to oligomerize into high-molecular-mass complexes in a cysteine disulfide Combretastatin A4 molecular weight bond-dependent manner, a biochemical feature also shared with holin proteins

[35]. Although the molecular details of how Cid and Lrg function to control cell death and lysis have not yet been completely elucidated, the fact that cid and lrg homologues have been identified in a wide variety of bacterial and archeal genomes supports a fundamental and conserved role for this system in cell physiology C59 mw [30, 36]. In previous work it was determined that expression of potential cidAB and lrgAB homologues in S. mutans is highly responsive to carbohydrate availability [12, 37] and oxygenation [11]. Given the potential importance of these genes to biofilm development in S. mutans, we previously characterized a panel of S. mutans cid and lrg isogenic mutants and found that a subset of these genes did indeed influence biofilm formation, production of glucosyltransferases (enzymes that synthesize extracellular glucan polymers that contribute to biofilm adhesion), and oxidative stress tolerance [37]. In this study it was also found that, as demonstrated previously in S. aureus[38, 39], the S. mutans LytST two-component system was required for activation of lrgAB expression, but not cidAB expression [37].

Our findings support the idea that a sustained M2 infiltration in tumor microenvironment could significantly limit selleck products the efficacy of BCG suggesting the need of a well planned therapeutical strategy in non-muscle PKC inhibitor invasive bladder cancer patients. References 1. Ferlay J, Parkin DM, Steliarova-Foucher E: Estimates of cancer incidence and mortality in Europe in 2008. Eur J Cancer 2010, 46:765–781.PubMedCrossRef 2. Fleming JD, Cooper JS, Jenson DE, et al.: AJCC cancer

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Koopman et al [52] found that after full-body resistance

training, adding carbohydrate (0.15, or 0.6 g/kg/hr) to amply dosed casein hydrolysate (0.3 g/kg/hr) did not increase whole body protein balance during a 6-hour post-exercise recovery period compared to the protein-only treatment. Subsequently, Staples et al [53] reported that after lower-body resistance exercise (leg extensions), the increase in post-exercise muscle protein balance from ingesting BI 10773 mw 25 g whey isolate was not improved by an additional 50 g maltodextrin during a 3-hour recovery period. For the goal of maximizing rates of muscle gain, these findings support the broader objective of meeting total daily carbohydrate need instead of specifically timing its constituent doses. Collectively, these data indicate an increased potential for dietary flexibility while maintaining the pursuit of optimal timing. References 1. Kerksick C, Harvey T, Stout J, Campbell B, Wilborn C, Kreider R, Kalman D, Ziegenfuss T, Lopez H, Landis J, Ivy JL, Antonio J: Inhibitor Library ic50 International Society of Sports Nutrition position stand: nutrient timing. J Int Soc Sports Nutr. 2008, 5:17.CrossRefPubMed 2. Ivy J, Portman R: Nutrient Timing: The Future of Sports Nutrition. North Bergen, NJ: Basic Health Publications; 2004. 3. Candow DG, Chilibeck PD: Timing of creatine or protein supplementation Belnacasan supplier and resistance training in the elderly. Appl Physiol Nutr Metab 2008,33(1):184–90.CrossRefPubMed 4. Hulmi JJ, Lockwood

CM, Stout JR: Effect of protein/essential amino acids and resistance training on skeletal muscle hypertrophy: A case for whey protein. Nutr Metab (Lond). 2010, 7:51.CrossRef 5. Kukuljan S, Nowson CA, Sanders K, Daly

RM: Effects of resistance exercise and fortified milk on skeletal muscle mass, muscle size, and functional performance in middle-aged and older men: an 18-mo randomized controlled trial. J Appl Physiol 2009,107(6):1864–73.CrossRefPubMed 6. Lambert CP, Temsirolimus Flynn MG: Fatigue during high-intensity intermittent exercise: application to bodybuilding. Sports Med. 2002,32(8):511–22.CrossRefPubMed 7. MacDougall JD, Ray S, Sale DG, McCartney N, Lee P, Garner S: Muscle substrate utilization and lactate production. Can J Appl Physiol 1999,24(3):209–15.CrossRefPubMed 8. Robergs RA, Pearson DR, Costill DL, Fink WJ, Pascoe DD, Benedict MA, Lambert CP, Zachweija JJ: Muscle glycogenolysis during differing intensities of weight-resistance exercise. J Appl Physiol 1991,70(4):1700–6.PubMed 9. Goodman CA, Mayhew DL, Hornberger TA: Recent progress toward understanding the molecular mechanisms that regulate skeletal muscle mass. Cell Signal 2011,23(12):1896–906.CrossRefPubMed 10. Bodine SC, Stitt TN, Gonzalez M, Kline WO, Stover GL, Bauerlein R, Zlotchenko E, Scrimgeour A, Lawrence JC, Glass DJ, Yancopoulos GD: Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo. Nat Cell Biol. 2001,3(11):1014–9.CrossRefPubMed 11.