نتایج جستجو برای: طبقهبندی jel q13

تعداد نتایج: 28603  

Journal: :International Journal of Advances in Engineering and Pure Sciences 2020

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2014

Journal: :Journal of medical genetics 2003
D C Bittel N Kibiryeva Z Talebizadeh M G Butler

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...

Journal: :European Journal of Economic and Financial Research 2023

<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...

Journal: :Afyon Kocatepe University Journal of Sciences and Engineering 2019

Journal: :Mehmet Akif Ersoy üniversitesi fen bilimleri enstitüsü 2021

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...

2006
Arthur H. Goldsmith Darrick Hamilton

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...

ژورنال: :genetics in the 3rd millennium 0
بهروز ابراهیمی behrouz ebrahimzadeh یوسف شفقتی yousef shafeghati نوید المدنی navid almadani روشنک وامقی roshank vameghi فیروزه ساجدی firouzeh sajedi ساغر قاسمی فیروز آبادی saghar ghasemi firouzabadi حسین نجم آبادی

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...

Journal: :Human molecular genetics 1999
S L Christian J A Fantes S K Mewborn B Huang D H Ledbetter

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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