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Vendor Name : CIW
Exam Code : 1D0-51B
Exam Name : CIW v5 Foundations SDF Module
Questions and Answers : 60 Q & A
Updated On : September 18, 2018
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1D0-51B Certification Brain Dumps Source : CIW v5 Foundations SDF Module

Test Code : 1D0-51B
Test Name : CIW v5 Foundations SDF Module
Vendor Name : CIW
Q&A : 60 Brain Dump Questions

CIW v5 Foundations SDF

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Heparanase enhances myeloma progression by the use of CXCL10 downregulation | killexams.com real questions with brain dumps

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    Folkman J, Klagsbrun M, Sasse J, Wadzinski M, Ingber D, Vlodavsky I. A heparin-binding angiogenic protein—simple fibroblast increase aspect—is kept within basement membrane. Am J Pathol 1988; one hundred thirty: 393–400.

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    Barash U, Cohen-Kaplan V, Arvatz G, Gingis-Velitski S, Levy-Adam F, Nativ O et al. A novel human heparanase splice variant, T5, endowed with protumorigenic qualities. FASEB J 2010; 24: 1239–1248.

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    Fux L, Feibish N, Cohen-Kaplan V, Gingis-Velitski S, Feld S, Geffen C et al. constitution-feature strategy identifies a COOH-terminal area that mediates heparanase signaling. melanoma Res 2009; 69: 1758–1767.

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    Cohen-Kaplan V, Doweck I, Naroditsky I, Vlodavsky I, Ilan N. Heparanase augments epidermal boom ingredient receptor phosphorylation: correlation with head and neck tumor progression. melanoma Res 2008; 68: 10077–10085.

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    Cohen-Kaplan V, Jrbashyan J, Yanir Y, Naroditsky I, Ben-Izhak O, Ilan N et al. Heparanase induces sign transducer and activator of transcription (STAT) protein phosphorylation: preclinical and clinical magnitude in head and neck melanoma. J Biol Chem 2012; 287: 6668–6678.

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    Riaz A, Ilan N, Vlodavsky I, Li JP, Johansson S. Characterization of heparanase-brought about phosphatidylinositol 3-kinase-AKT activation and its integrin dependence. J Biol Chem 2013; 288: 12366–12375.

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    Cohen-Kaplan V, Naroditsky I, Zetser A, Ilan N, Vlodavsky I, Doweck I. Heparanase induces VEGF C and enables tumor lymphangiogenesis. Intl J cancer 2008; 123: 2566–2573.

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    Nadir Y, Brenner B, Zetser A, Ilan N, Shafat I, Zcharia E et al. Heparanase induces tissue ingredient expression in vascular endothelial and cancer cells. J Thromb Haemost 2006; four: 2443–2451.

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    Yang Y, Ren Y, Ramani VC, Nan L, Suva LJ, Sanderson RD. Heparanase enhances local and systemic osteolysis in multiple myeloma by way of upregulating the expression and secretion of RANKL. melanoma Res 2010; 70: 8329–8338.

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    Okawa T, Naomoto Y, Nobuhisa T, Takaoka M, Motoki T, Shirakawa Y et al. Heparanase is involved in angiogenesis in esophageal cancer via induction of cyclooxygenase-2. Clin cancer Res 2005; eleven: 7995–8005.

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    Ramani VC, Yang Y, Ren Y, Nan L, Sanderson RD. Heparanase performs a twin function in driving hepatocyte increase aspect (HGF) signaling via enhancing HGF expression and undertaking. J Biol Chem 2011; 286: 6490–6499.

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    Nadav L, Katz BZ, Baron S, Cohen N, Naparstek E, Geiger B. The generation and regulation of purposeful diversity of malignant plasma cells. melanoma Res 2006; 66: 8608–8616.

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    Purushothaman A, Uyama T, Kobayashi F, Yamada S, Sugahara okay, Rapraeger AC et al. Heparanase-more advantageous shedding of syndecan-1 through myeloma cells promotes endothelial invasion and angiogenesis. Blood 2010; 115: 2449–2457.

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    Gingis-Velitski S, Zetser A, Flugelman MY, Vlodavsky I, Ilan N. Heparanase induces endothelial mobile migration by means of protein kinase B/Akt activation. J Biol Chem 2004; 279: 23536–23541.

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    Beider ok, begin M, Abraham M, Wald H, Weiss id, Wald O et al. CXCR4 antagonist 4F-benzoyl-TN14003 inhibits leukemia and dissimilar myeloma tumor boom. Exp Hematol 2011; 39: 282–292.

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    Zetser A, Bashenko Y, Edovitsky E, Levy-Adam F, Vlodavsky I, Ilan N. Heparanase induces vascular endothelial growth ingredient expression: correlation with p38 phosphorylation tiers and Src activation. melanoma Res 2006; 66: 1455–1463.

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    Meiron M, Zohar Y, Anunu R, Wildbaum G, Karin N. CXCL12 (SDF-1alpha) suppresses ongoing experimental autoimmune encephalomyelitis through opting for antigen-particular regulatory T cells. J Exp Med 2008; 205: 2643–2655.

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    Barash U, Arvatz G, Farfara R, Naroditsky I, Doweck I, Feld S et al. clinical magnitude of heparanase splice variant (t5) in renal cellphone carcinoma: assessment by way of a novel t5-particular monoclonal antibody. PLoS One 2012; 7: e51494.

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    Arvatz G, Barash U, Nativ O, Ilan N, Vlodavsky I. submit-transcriptional legislation of heparanase gene expression by using a 3′ AU-prosperous element. FASEB J 2011; 24: 4969–4976.

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    Miao HQ, Liu H, Navarro E, Kussie P, Zhu Z. building of heparanase inhibitors for anti-cancer remedy. Curr Med Chem 2006; 13: 2101–2111.

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    Purushothaman A, Babitz SK, Sanderson RD. Heparanase enhances the insulin receptor signaling pathway to activate extracellular sign-regulated kinase in assorted myeloma. J Biol Chem 2012; 287: 41288–41296.

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    Purushothaman A, Chen L, Yang Y, Sanderson RD. Heparanase stimulation of protease expression implicates it as a grasp regulator of the aggressive tumor phenotype in myeloma. J Biol Chem 2008; 283: 32628–32636.

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    Sanderson RD, Iozzo RV. targeting heparanase for cancer remedy on the tumor-matrix interface. Matrix Biol 2012; 31: 283–284.

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    Feldman AL, Friedl J, Lans TE, Libutti SK, Lorang D, Miller MS et al. Retroviral gene switch of interferon-inducible protein 10 inhibits increase of human melanoma xenografts. Intl J melanoma 2002; ninety nine: 149–153.

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    Man ok, Ng KT, Xu A, Cheng Q, Lo CM, Xiao JW et al. Suppression of liver tumor increase and metastasis by way of adiponectin in nude mice through inhibition of tumor angiogenesis and downregulation of Rho kinase/IFN-inducible protein 10/matrix metalloproteinase 9 signaling. Clin cancer Res 2010; sixteen: 967–977.

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    solar Y, Finger C, Alvarez-Vallina L, Cichutek k, Buchholz CJ. chronic gene start of interferon-inducible protein 10 via replication-capable retrovirus vectors suppresses tumor growth. cancer Gene Ther 2005; 12: 900–912.

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    Tannenbaum CS, Tubbs R, Armstrong D, Finke JH, Bukowski RM, Hamilton TA. The CXC chemokines IP-10 and Mig are vital for IL-12-mediated regression of the mouse RENCA tumor. J Immunol 1998; 161: 927–932.

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    Sgadari C, Angiolillo AL, Cherney BW, Pike SE, Farber JM, Koniaris LG et al. Interferon-inducible protein-10 recognized as a mediator of tumor necrosis in vivo. Proc Natl Acad Sci country 1996; 93: 13791–13796.

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    Lamy L, Ngo VN, Emre NC, Shaffer AL3rd, Yang Y, Tian E et al. manage of autophagic mobile dying via caspase-10 in varied myeloma. cancer telephone 2013; 23: 435–449.

  • fifty five.

    Veitonmaki N, Hansson M, Zhan F, Sundberg A, Lofstedt T, Ljungars A et al. A human ICAM-1 antibody remoted with the aid of a function-first strategy has potent macrophage-based antimyeloma undertaking in vivo. cancer telephone 2013; 23: 502–515.


  • Overexpression of protein kinase C | killexams.com real questions with brain dumps

    The study become reviewed and authorized by the Institutional Ethics Committee on Animal components of the Anzhen clinic and Beijing Institute of heart, Lung, and Blood Vessel ailments, and conformed to the guiding principles of the ‘e-book for the Care and Use of Laboratory Animals’ (NIH ebook no. eighty three-23, revised 1996).

    Isolation, enlargement and passage of rat BMMSCs

    BMMSCs have been remoted and passaged as described up to now.forty two briefly, the femurs of Sprague–Dawley rats (male, 100–a hundred and twenty g) had been amassed after killing animal with the aid of cervical dislocation, and BMMSCs had been separated with Histopaque-1083 isolating medium (Sigma-Aldrich, St. Louis, MO, united states). Cells had been centrifuged at 1000 × g for 10 min and suspended in Dulbecco’s modified Eagle's medium with low glucose (GIBCO, Carlsbad, CA, united states of america) supplemented with 10% fetal bovine serum (Hyclone, Logan, UT, usa). After cells have been vaccinated in a way of life flask (2 × one zero five cells/cm2) and incubated at 37 °C with 5% CO2 and saturated humidity, the adherent layer became washed as soon as each 2 days with sparkling medium. Cells from passages four–eight had been harvested and used in subsequent biochemical experiments.

    Viability assay and increase of MSCs

    MSCs viability was measured with Trypan blue exclusion assay; plausible cells were counted. telephone viability (%) become calculated as the percent of cells missing dye. MSCs from passage 5 have been digested with 0.25% trypsin and added to 96-smartly plates (2 × 104 cells/ml; 200 μl per well) and cultured for eight consecutive days. The optical density (OD) and telephone counts have been measured each day. OD (570 nm) was measured after incubating cells with 20 μl 5 mg/ml methyltetrazolium for 4 h adopted through addition of one hundred fifty μl DMSO. A culture answer devoid of cells turned into a blank handle. telephone counts were carried out the usage of Trypan blue and boom curves were made. population doubling time (TD)=t[log2/(logNt–logN0)].

    Identification of MSCs floor markers by using circulate cytometry

    After cells had been digested with 2.5 g/l trypsin, MSCs have been prepared (1 × 106/ml) and incubated for 30 min at 37 °C with monoclonal antibodies towards CD29, CD44, CD34 and CD45. Cells have been centrifuged and washed thrice with PBS and incubated for 30 min with the corresponding FITC-labeled secondary antibody (see Supplementary Tables S2 and S3 for antibody data). Homologous IgG and PBS were poor controls. Expression levels of MSC surface markers were analyzed by way of circulate cytometry.

    construction of PKCɛ-overexpressed MSCs with the aid of gene switch

    PKCɛ-overexpressed lentiviruses had been based as described in the past.43 in brief, cDNA fragments of PKCɛ became obtained by PCR and cloned into the lentiviral vector (pLenti7.three/V5-TOPO) carrying an enhanced GFP (EGFP) reporter gene. The a success construction of PKCɛ-overexpressed vector changed into proven by way of sequencing. Then packaged and transferring vectors were co-transfected into 293T cells. consequently, lentiviral options – lenti-PKCɛ-EGFP and lenti-EGFP solutions – were bought. Virus titer become measured and MSCs from passage 4 have been plated and cultured unless eighty% confluent and had been contaminated with lenti-PKCɛ-EGFP or lenti-EGFP answer. Spare virus particles had been removed by using altering fresh medium. After 24 h, uninfected MSCs were removed with the aid of adding 2 μg/ml puromycin (puromycin resistance gene had been inserted into lentiviral vectors) and incubating for one more 24 h. Then, two MSCs, MSCs-GFP and MSCs-PKCɛ-GFP, were got. The floor markers of MSCs have been identified by means of move cytometry. After another two passages, transfected MSCs (passage 7) had been used for transplantation. choicest multiplicity of infection (virus particle counts/cellphone counts) and transfection effectivity had been measured. Transfection efficiency=(mobile counts expressing GFP/total cell counts) × a hundred%. Expression of PKCɛ in MSCs changed into established by means of actual-time PCR, western blot and immunocytochemistry.

    establishment of a rat AMI mannequin

    A rat AMI mannequin turned into centered via ligating the left anterior descending department (LAD) of the coronary artery as described up to now.44 All rats were anesthetized with 1% pentobarbital (40 mg/kg, i.p.) before surgical procedure. Tracheal cannula and ventilators had been connected for respiratory guide, and the dermis became incised alongside the left sternal border and the third and fourth ribs have been clipped, as hearts have been uncovered. Then, LADs had been ligated. To reap a standardized reasonable infarct measurement in each community, we ligated LADs at 1.5 mm beneath the stage of the inferior margin of the left auricle to obtain infarction sizes of 30–forty% with suited death expense. The myocardium in the anterior wall and the apex of the coronary heart under the ligation factor became white and had big hypomotility. ST phase elevation surpassed 1 mv in lead I and lead AVL after a hit ligation of LAD. Electrocardiogram monitoring and fluid dietary supplements were administrated throughout surgical procedure, and warmth upkeep and prophylactic anti-an infection therapy with penicillin got for 3 days after surgical procedure. identical processes have been performed except LAD ligation within the sham neighborhood.

    Experimental protocol in vivo

    Rats (eight weeks of age) had been divided into seven medication groups (n=16): sham community (sham); AMI group (AMI); AMI+MSCs community (MSCs); AMI+MSCs-GFP neighborhood (MSCs-GFP); AMI+MSCs-PKCɛ-GFP community (MSCs-PKCɛ); AMI+MSCs-PKCɛ-GFP+AMD3100 (CXCR4 antagonist) group (AMD3100); and the AMI+MSCs-PKCɛ-GFP+LY294002 (PI3K inhibitor) group (LY294002). One hour after LAD ligation, remedy solution changed into injected into 5 different sites in the infarct border zone (1 × 106 MSCs, 20 μl for every injection web page) found on the juncture between white and hypokinetic myocardium and common myocardium. Suture marks had been made at the critical aspects of transplanted zones. subculture media devoid of MSC’s had been handle injections (sham and AMI community). The medicine options for the MSCs, MSCs-GFP and MSCs-PKCɛ corporations contained MSCs, MSCs-GFP and MSCs-PKCɛ-GFP, respectively. MSCs in the AMD3100 and LY294002 organizations have been pretreated with AMD3100 and LY294002, respectively, for 24 h before being administered.

    After transplantation (24 h), rats had been killed the use of 3% pentobarbital sodium (a hundred mg/kg, i.p.), and hearts were harvested and cardiac tissues in the infarct border zones had been accrued to operate subsequent biochemical evaluation. Retention of transplanted MSCs and affiliation with PKCɛ distribution were measured with immunofluorescent staining and we measured mRNA, and protein expression of signal proteins in PKCɛ, SDF-1/CXCR4 and PI3K/AKT pathways the use of true-time PCR and western blot.45

    four weeks after transplantation, echocardiographic measurements had been performed on all rats and subsets of animals had been killed as outlined above. Distributions of transplanted MSCs had been analyzed by means of immunofluorescence to examine the results of PKCɛ on MSC survival. Apoptotic evaluation become carried out with TdT-mediated dUTP nick end labeling (TUNEL) assay and mRNA and protein expression of VEGF, bFGF and TGFβ were quantified with precise-time PCR and western blot, respectively. cTnI, vWF and SMA are peculiarly expressed in myocytes, vascular endothelial cells and vascular easy muscle cells, respectively, and their expression, distribution and relationship with transplanted MSCs had been analyzed by way of immunofluorescence to ascertain effects of PKCɛ on cardiac differentiation of MSCs. Myocardial tissue sections and vascular endothelial telephone marker component VIII have been quantified with immunohistochemistry, and vessels were counted and vessel densities had been measured. Histology became additionally used to check cardiac tissue.

    Echocardiographic measurements

    Echocardiographic measurements have been carried out on all rats before ligation and at 4 weeks after transplantation, and EF, FS, LVEDD and LVESD, IVSd and LVmass were measured using a HP SONOS 5500 sector scanner (Hewlett Packard CO, Andover, MA, us of a) with a 7.5 MHz imaging transducer.

    real-time reverse transcription-PCR evaluation of mRNA of primary proteins

    total RNA changed into extracted from tissue homogenate in each and every community with RNA elementary complete RNA equipment (TIANGEN, Peking, China). cDNA changed into prepared using an iScript cDNA Synthesis kit (Bio-Rad, Hercules, CA, usa) and actual-time PCR turned into performed on samples the usage of an Exicycler 96 (Bioneer, Daejeon, Korea) according to the company’s protocol. mRNA expression of proteins of interest had been measured. Primer sequences used are listed in Supplementary table S1. Amplification and melting curves have been acquired, and β-actin became the reporter gene. an easy primer reaction product was a bad control.

    Western blot to quantify major protein expression

    Samples had been plated in 24-neatly dishes (50 000 cells per smartly) and harvested in 50 μl pattern buffer, boiled and sonicated. Protein lysates had been separated with 10% sodium dodecyl sulfate polyacrylamide gel electropheresis and gels have been transferred polyvinylidene fluoride membranes and blocked with nonfat milk (5% w/v). Then, blots had been incubated with basic antibodies in a single day at four °C, adopted by incubation with horseradish peroxidase-conjugated secondary antibody for 45 min at 37 °C. Bands had been measured with improved chemiluminescence (Applygen, Peking, China) and quantified using laser densitometry with a typhoon 9400 fluorescent scanner and ImageQuant TL 5.0 software (GE Healthcare, Buckinghamshire, UK) as previously described.forty fiveβ-Actin changed into an interior reference (antibody suggestions see Supplementary table S2).

    Immunofluorescence evaluation

    After fixing in acetone solution at 4 °C for 15 min, cryosections of cardiac tissue had been washed thrice with PBS and blocked with goat serum for 30 min after which incubated with fundamental antibodies at four °C in a single day. After washing three times, cryosections have been incubated with fluorescent-labeled secondary antibodies (Supplementary desk S4) at midnight for ninety min, and then counterstained with four',6-diamidino-2-phenylindole. An anti-fluorescence quench agent become added to the cryosections and sections were accompanied beneath a Confocal Laser Scanning Microscope (Olympus, Tokyo, Japan). The distribution of transplanted MSCs and protein expression turned into assessed with picture-pro Plus 6.0 application (Media Cybernetics, Rockville, MD, usa), and GFP-superb cells and protein-nice cells were counted.

    Apoptosis assay

    TUNEL assay was used with an In Situ telephone demise Detection package (Roche, Basel, Switzerland) in accordance with the company guidelines (Supplementary table S5). Tissue samples in each and every community had been embedded in paraffin, and sections had been made and incubated 60 min with TUNEL reaction blend at 37 °C at nighttime. Samples have been then incubated for 30 min with converter-peroxidase answer at 37 °C adopted by using coloring with diaminobenzidine (DAB) and counterstaining with hematoxylin. Apoptosis changed into quantified microscopically and an apoptosis index turned into calculated.

    Immunohistochemistry

    After deparaffination, cardiac tissue sections have been incubated in three% H2O2 for 15 min and blocked with goat serum for 15 min after which incubated with simple antibody, component VIII antibody overnight at 4 °C. After washing thrice, sections were incubated with biotin-labeled secondary antibodies at 37 °C for 30 min, and sections have been incubated with horseradish peroxidase labeled SA streptavidin at 37 °C for 30 min. Then, sections were stained with DAB and counterstained with hematoxylin. aspect VIII expression and vessel counts had been quantified microscopically (for antibody tips see Supplementary table S6).

    Histological experiences

    All rats have been killed as described above after echocardiographic measurements four weeks after transplantation. Myocardial infarct measurement changed into measured by using 2,three,5,triphenyl-2H-tetrazolium chloride (TTC) as described in the past.forty six briefly, after echocardiographic examine, the LAD was re-occluded, and patent blue dye turned into administered intravenously to stain commonplace regions of the left ventricle (LV), and the heart become impulsively excised. LV tissue changed into isolated and cut into approximately 10 go-sectional pieces of equal thickness. Nonstained LV areas in danger (AAR) have been separated from the encompassing blue-stained LV normal zone, and both regions had been one after the other incubated for 15 min at 37 °C in 1% TTC in 0.1 M phosphate buffer adjusted to pH 7.4. Tissues had been fixed overnight in 10% formaldehyde. AAR and blue-stained LV regular zones have been weighed to determine AAR/LV. TTC stains dwelling tissue a deep pink color, but necrotic tissue appears white in the AAR slices. every slice became scanned with a business scanner (Canoscan LiDE 60, Canon, Tokyo, Japan), and infarcted and noninfarcted areas had been measured the use of an image analysis application. Myocardial infarct size changed into expressed as a percentage of the AAR.

    additionally, rat heart tissues had been fastened in neutral formalin for histology and embedded in paraffin. Then, 5 μm serial go sections have been made and stained with hematoxylin and eosin. 5 fields and 20 myocardial cells per field had been selected randomly, and general diameters have been calculated. Observations have been made on coded samples by an independent observer blinded to animal identify. After deparaffination, sections of cardiac tissue had been dripped into 1% Picro sirius pink saturated trinitrophenol answer for 1 h followed through washing for five min. Then sections have been counterstained with hematoxylin answer for 5 min adopted with the aid of washing for 1 min. Sections had been put in 1% hydrochloric acid alcohol for three s followed by means of washing for 20 min. Collage expression levels in every neighborhood had been measured microscopically and myocardial interstitial collagen area percents [(collagen area/total area) × 100%] have been derived.

    Statistical analysis

    All values are ability±S.D. differences in continuous variables between two businesses have been analyzed by way of the scholar’s t-examine, and variations amongst three or extra businesses had been evaluated by way of one-approach ANOVA with Bonferroni correction. differences in categorical statistics have been assessed the usage of a Chi-rectangular test, or in case of low telephone counts (<5), Fisher’s accurate check was used; P<0.05 became regarded to be big.




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