نتایج جستجو برای: تریسومی آزاد 21

تعداد نتایج: 271563  

Journal: :Science 2009
Anja Fröhlich Jan Kisielow Iwana Schmitz Stefan Freigang Abdijapar T Shamshiev Jacqueline Weber Benjamin J Marsland Annette Oxenius Manfred Kopf

Chronic viral infection is often associated with the dysfunction of virus-specific T cells. Our studies using Il21r-deficient (Il21r-/-) mice now suggest that interleukin-21 (IL-21) is critical for the long-term maintenance and functionality of CD8+ T cells and the control of chronic lymphocytic choriomeningitis virus infection in mice. Cell-autonomous IL-21 receptor (IL-21R)-dependent signalin...

2016
Parvin Farzanegi

The aim of this study is to determine the effects of aerobic training on serum FGF21 levels and glucose in women with type II diabetes mellitus. Women with type II diabetes mellitus were divided into two groups including control (n=14) and aerobic training (n=14) the mean levels of serum FGF21, glucose were measured in all participants after 8 weeks exercise. The mean of FGF21 levels after exer...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه گیلان - دانشکده علوم پایه 1392

این مطالعه به بررسی تفاوت در متیلاسیون دو ژن aire و rassf1a بین مادر و جنین و استفاده از این تفاوت در شناسایی dna آزاد جنینی در پلاسمای مادر در تشخیص پیش از تولد تریزومی 21 می پردازد. از 30 خانم باردار که دارای جنین تک قلو بودند، نمونه خون گرفته شد. همچنین از آن ها نمونه مایع آمنیوتیک برای بررسی کاریوتایپ، تهیه گردید. جهت تشخیص تریزومی 21 از تفاوت در متیلاسیون دو ژن rassf1a و aire از آنزیم های ...

2015
Tomohiro Ishii Makoto Anzo Masanori Adachi Kazumichi Onigata Satoshi Kusuda Keisuke Nagasaki Shohei Harada Reiko Horikawa Masanori Minagawa Kanshi Minamitani Haruo Mizuno Yuji Yamakami Masaru Fukushi Toshihiro Tajima

Purpose of developing the guidelines: The first guidelines for diagnosis and treatment of 21-hydroxylase deficiency (21-OHD) were published as a diagnostic handbook in Japan in 1989, with a focus on patients with severe disease. The "Guidelines for Treatment of Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) Found in Neonatal Mass Screening (1999 revision)" published in 1999 were rev...

Journal: :Internal medicine 2009
Rui Imamine Hiroshi Arima Miho Kusakabe Hiroshi Umeda Ikuko Sato Keiko Homma Takeshi Usui Yutaka Oiso

We report two Japanese women with androgen excess symptoms. Analyses of 21-hydroxylase gene demonstrated that a 24-year-old Japanese woman had a homozygous mutation of IVS2-13 A/C>G, while a 25-year-old Japanese woman had a compound heterozygous mutation of I172N and E245del1nt, a novel mutation which would result in completely nonfunctional enzyme due to a frame shift. As IVS2-13 A/C>G and I17...

Journal: :Lexikos 2012

Journal: :Rheumatology Advances in Practice 2019

Journal: :Plastic and Reconstructive Surgery - Global Open 2020

Journal: :Philologus 1863

Journal: :Optics and Spectroscopy 2022

We report Zeeman infra-red spectroscopy of electronic-nuclear levels 5I8 →5I7 transitions Ho3+ in the C4v(F−) centre CaF2 with magnetic field along ⟨111⟩ direction crystal. Transitions to lowest 5I7 state, an isolated electronic doublet, and next group states, a pseudo-quadruplet consisting doublet two nearby singlets, exhibit strongly non-linear splittings intensity variations. Simulated spect...

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