نتایج جستجو برای: e200
تعداد نتایج: 26 فیلتر نتایج به سال:
مقدمه: دیسمنوره اولیه، یکی از اختلالات شایع دستگاه تناسلی است. راههای متفاوتی جهت درمان دیسمنوره مطرح است. مطالعه حاضر با هدف تعیین تأثیر کپسول منستروگل (عصاره خشک کرفس، زعفران و انیسون) و ویتامین E بر شدت دیسمنوره اولیه انجام شد. روش کار: این مطالعه کارآزمایی بالینی دوسوکور در سال 1396 بر روی 120 دختر دانشجوی علوم پزشکی همدان با دیسمنوره اولیه انجام شد. افراد به‌صورت بلوک جایگشتی در 3 گروه 4...
<div id="contentsContainer" class="style-scope qowt-page"><div id="contents" qowt-page"><p id="E129" class="x-scope qowt-word-para-4"><strong><span id="E130" class="qowt-font2-Arial">ABSTRAK </span></strong></p><p id="E131" qowt-word-para-5"><span id="E132" class="qowt-font2-Arial"><strong>Latar Belakang:</strong> </span...
Peptidoglycan hydrolases are key enzymes in bacterial cell wall homeostasis. Understanding the substrate specificity and biochemical activity of peptidoglycan hydrolases in Mycobacterium tuberculosis is of special interest as it can aid in the development of new cell wall targeting therapeutics. In this study, we report biochemical and structural characterization of the mycobacterial Nacetylmur...
•Periodontitis is associated with hematologic changes (SORT A recommendation).•Higher leukocyte, neutrophil, and erythrocyte sedimentation rates are the most common findings.•Periodontitis treatment was a decrease in leukocyte levels. Periodontitis chronic inflammatory disease local systemic implications. Evidence suggests consistent periodontitis. Our aim to critically appraise available evide...
The destination of peroxisomal matrix proteins is encoded by short peptide sequences, which have been characterized as peroxisomal targeting signals (PTS) residing either at the C-terminus (PTS1) or close to the N-terminus (PTS2). PTS2-carrying proteins interact with their cognate receptor protein PEX7 that mediates their transport to peroxisomes by concerted action with a co-receptor protein, ...
Objective: To provide new insights into the interpretation of genetic variants in a rare neurologic disorder, CDKL5 deficiency, in the contexts of population sequencing data and an updated characterization of the CDKL5 gene. Methods: We analyzed all known potentially pathogenic CDKL5 variants by combining data from large-scale population sequencing studies withCDKL5 variants from new and all av...
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