Results for a minimum age applies to all acti... translation from English to Persian

and applies to all jews over 12 years of age .
و تمام يهودياني که بالاتر از دوازده سال دارند به اين حکم عمل خواهند کرد .

& apply to all sheets
تنظی٠٠قادیر

& apply to all remaining files
& اعمال به همۀ پرونده‌های باقی‌مانده‌

while this theory seems to fit most of the secular and some of the religious figures, it does not apply to all of them.
این نظریه بیشتر از این واقعیت سرچشمه می‌گیرد که در ایرلند به برخی از این پیکره‌های سنگی، سنگ‌های چشم زخم گفته می‌شود.

this filter is applied to text jobs of the specified language. you may select more than one language by clicking the browse button and ctrl-clicking on more than one in the list. if blank the filter applies to all text jobs of any language.
این پالایه برای کارهای متن زبان مشخص‌شده به کار می‌رود‌‌. ممکن است بیش از یک زبان را با فشار دکمۀ مرور و فشار مهار روی بیش از یک زبان در فهرست برگزینید‌‌. در صورت فاصله ، پالایه برای همۀ کارهای متن هر زبانی به کار می‌رود‌.

they are universal; that is, they apply to all people, and do not derive from the laws of any specific society.
* حق‌العمل: کارمزد، پولی که بابت فروش کالایی از صاحب کالا دریافت کنند یا بابت انجام سفارشی از سفارش‌دهنده بگیرند.

this filter will be applied only to text having the specified doctype specification. if blank, applies to all text. you may enter more than one doctype separated by commas. example: "xhtml".
این پالایه تنها برای متنهایی که مشخصۀ doctype مشخص‌شده دارند ، اعمال می‌شود‌‌. اگر فاصله باشد ، در همۀ متنها اعمال می‌شود‌‌. ممکن است بیش از یک doctype که با کاما از هم جدا شده‌اند ، وارد کنید‌‌. مثال: » xhtml« ‌.

the sample size was estimated using the g*power 3.0.10 software, setting the alpha level at 0.05 and power at 80%. the effective sample size was calculated as 0.20. based on these criteria, the ideal number of participants in each group was calculated to be 16, which generated a total sample size of 64. following clearance from the institutional ethics committee (certificate no: kids/iec/nov-2019/36), 16 volunteering subjects who met the inclusion and exclusion criteria were recruited for this prospective double-blind, split-mouth, randomized placebo controlled trial after signing an informed consent document, in accordance with the declaration of helsinki (2013) (figure 2) (clinical trials registry of india registration no: ctri/2019/12/022458). a single examiner enrolled systemically healthy individuals aged 30-50 years, diagnosed with stage 3 grade b generalized periodontitis, with a minimum of 20 teeth and at least one site with a probing pocket depth (ppd) of >5mm and clinical attachment level (cal) of 2mm or greater in each of the four quadrants.7 this study did not include subjects who had undergone periodontal therapy or were administered antibiotics or immunosuppressants until 6 months before the study began, chronic smokers, alcoholics, non-smoking tobacco users, subjects with acute illnesses/acute intraoral lesions, pregnant women and lactating mothers, and medically compromised subjects. after a clinical examination the recording of clinical and microbiological parameters at baseline and a full mouth srp were conducted and each subject’s 4 quadrants were randomly assigned to one of the following treatment groups through a simple, computer-generated randomization technique: group 1 (control) – application of placebo gel followed by sham pct (directing the light cure device without turning on the light beam). group 2 – application of nano zno gel followed by sham pct. group 3 – application of placebo gel followed by pct. group 4 – application of nano zno gel followed by pct. the interventions for each group were performed on all periodontal pockets in the assigned quadrant at baseline, at the end of the first week and 1 month after the first session. the interventions were allocated to the quadrants using sealed opaque envelopes. on the day of intervention, each subject chose one envelope to detect their randomized allocation. in each quadrant, the tooth with the deepest ppd was chosen as the test site. the microbiological sampling and the assessment of clinical parameters were performed at baseline (prior to srp), at 1 month from baseline and 3 months from it. these procedures were carried out by a single examiner who was blinded to all the study groups. the intra-operator reliability test carried out to establish reproducibility of the results was found to be substantial (cohen’s kappa-0.8), with an observed percentage agreement of more than 75%.
حجم نمونه با استفاده از نرم افزار g*power 3.0.10 برآورد شد و سطح آلفا 05/0 و توان 80 درصد را تعیین کرد. حجم نمونه موثر 20/0 محاسبه شد. بر اساس این معیارها، تعداد ایده آل شرکت کنندگان در هر گروه 16 نفر محاسبه شد که حجم نمونه کل 64 نفر را به خود اختصاص داد. پس از اخذ مجوز از کمیته اخلاق نهادی (گواهی شماره: kids/iec/nov 1398/36)، 16 نفر از آزمودنی های داوطلب که معیارهای ورود و خروج را داشتند برای این مطالعه انتخاب شدند.