نتایج جستجو برای: طبقهبندی jel q13
تعداد نتایج: 28603 فیلتر نتایج به سال:
BACKGROUND Prader-Willi syndrome (PWS), the most common genetic cause of marked obesity, is caused by genomic imprinting and loss of expression of paternal genes in the 15q11-q13 region. There is a paucity of data examining simultaneous gene expression in this syndrome. METHODS We generated cDNA microarrays representing 73 non-redundant genes/transcripts from the 15q11-q13 region, the majorit...
<p>The study focuses on the impact of strategic leadership competitive advantage by applying it to horticultural sector in Sudan, Khartoum State, is an applied and analytical carried out periods (2013-2022). The statement research problem that, there a defect as result improper application leadership. main question was applying, horticulture State? aims at identifying relationship between...
Aloe vera (AV) süt, dondurma, şekerleme, sağlık içecekler gibi fonksiyonel gıdalarda kullanılmaktadır. Yapılan bu araştırmada, yoğurt kültürüne probiyotik ve teknolojik özelliklere sahip olan Lactobacillus plantarum AB6-25 suşu, %1, 2,5 5 oranlarında AV jel içeceği ilave edilerek üretimi yapılmıştır. Depolamanın 1, 7, 14 21. günlerinde üretilen yoğurtların fizikokimyasal, mikrobiyolojik analizl...
JEL Classification Code(s): J 31, J 71) "Perceptions of Discrimination, Effort to Obtain Psychological Balance, and Relative Wages: Can We Infer a Happiness Gradient?" There is a substantial literature that finds a linkage between happiness and relative economic well being as measured by earnings or wages. There is also a well documented racial gap in wages. One explanation for this is disparat...
سندرم آنجلمن یک اختلال ژنتیکی پیچیده است که سیستم عصب مرکزی را گرفتار می کند . اغلب موارد سندرم آنجلمن (حدود 70%) زمانی رخ می دهد که یک قطعه از کروموزوم 15 (15q11-q13)مادری حذف میشود . علایم اصلی این سندرم شامل تاخیر تکامل ، ناتوانی ذهنی، اختلال کلامی شدید و مشکلات حرکتی و تعادلی ( آتاکسیا) میباشد . در این گزارش یک پسر بچه 8 ساله با علایم ناتوانی ذهنی ، تشنج ، خنده اضافی و اختلال حرکتی در دستها...
The most common etiology for Prader-Willi syndrome and Angelman syndrome is de novo interstitial deletion of chromosome 15q11-q13. Deletions and other recurrent rearrangements of this region involve four common 'hotspots' for breakage, termed breakpoints 1-4 (BP1-BP4). Construction of an approximately 4 Mb YAC contig of this region identified multiple sequence tagged sites (STSs) present at bot...
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