نتایج جستجو برای: pank2 gene

تعداد نتایج: 1141396  

Journal: :iranian journal of basic medical sciences 0
lin liu department of hematology, the second affiliated hospital of kunming medical university, kunming 650101, china lin tan department of hematology, the first affiliated hospital of kunming medical university, kunming 650041, china zhenxin he department of hematology, the first affiliated hospital of kunming medical university, kunming 650041, china

objective(s): the aim of this study was to investigate the methylation status and mrna expression levels of p15, death-associated protein kinase (dapk), and suppressor of cytokine signaling-1 (socs1) genes in multiple myeloma (mm). materials and methods: the bone marrow samples of 54 mm patients were collected and the methylation status of the p15, dapk, and socs1 gene promoter regions was dete...

Journal: :iranian red crescent medical journal 0
hamid alavi majd department of biostatistics, school of paramedical sciences, shahid beheshti university of medical sciences, tehran, ir iran atefeh talebi department of biostatistics, school of paramedial sciences, students’ research committee, shahid beheshti university of medical sciences, tehran, ir iran; department of biostatistics, school of paramedial sciences, students’ research committee, shahid beheshti university of medical sciences, tehran, ir iran. tel: +98-2122707347, fax: +98-2122721150 kambiz gilany reproductive biotechnology research center, avicenna research institute, acecr, tehran, ir iran nasibeh khayyer proteomics research center, shahid beheshti university of medical sciences, tehran, ir iran

conclusions some results of the correlation coefficients are not the same with visualization. the reason may be due to the small number of data. materials and methods in the foundation-application study, we constructed two-way gene networks using nonparametric methods, such as spearman’s rank correlation coefficient and blomqvist’s measure, and compared them with pearson’s correlation coefficie...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس 1381

ماکروفاژها از سلولهای مهم سیستم ایمنی در پاسخ به عوامل بیماریزای مختلف از جمله ویروس هرپس سیمپلکس یک 1- ‏‎hsv0 هستند و عوامل موثر بر فعالیت آنها می توانند در سرنوشت بیماری موثر باشند. در این مطالعه اثر نوروپپتیدهای ‏‎substance p(sp)‎‏ و‏‎calcitonin gene related-peptide‎‏ (‏‎cgrp‎‏) که تحت شرایطی مثل استرس و التهاب از رشته های عصبی حسی آزاد می شوند و دارای گیرنده فعال بر روی ماکروفاژها می باشند ...

Journal: :genetics in the 3rd millennium 0
abolfazl barzegari alireza ostadrahimi vahideh ebrahimzadeh attari abolfazl gorbani

in view of the fundamental role of genetics in development of obesity, the present study aimed to investigate the single nucleotide polymorphism of some obesity-related genes among a subset of obese women living in tabriz, iran. for this purpose, 70 eligible obese women (aged 18-45 years) were genotyped for the uncoupling protein-1 (ucp-1) -3826a>g, ß3-adrenergic receptor (ß3adr) trp64arg, lept...

2014
Badreeddine Alami Siham Tizniti

La maladie d'Hallervorden-Spatz est une affection autosomique récessive très rare. Elle débute essentiellement entre 5 et 12 ans, mais parfois même dans la première année de la vie. Des cas débutant chez l'adulte jeune ont été rarement rapportés. Sa symptomatologie comporte des signes extra-pyramidaux associant: rigidité, mouvements choréo-athétosiques, dystonie, dysarthrie, détérioration intel...

Journal: :medical journal of islamic republic of iran 0
amir mehrgou department of medical genetics and molecular biology, school of medicine, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences) mansoureh akouchekian department of medical genetics and molecular biology, school of medicine, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences)

many factors including genetic, environmental, and acquired are involved in breast cancer development across various societies. among all of these factors in families with a history of breast cancer throughout several generations, genetics, like predisposing genes to develop this disease, should be considered more. early detection of mutation carriers in these genes, in turn, can play an import...

Afagh Alavi, Mohammad Masoud Rahimi Bidgoli, Mohammad Rohani, Reza Hajati,

Neurodegeneration with brain iron accumulation (NBIA) is a rare set of inherited neurodegenerative disorders with abnormal accumulation of iron in basal ganglia. It is a clinically and genetically heterogeneous disorder that is characterized by movement disorders, dystonia, dysarthria, Parkinsonism, intellectual disability, and spasticity. The age at onset varies from childhood to adulthood and...

Journal: :Journal of the neurological sciences 2005
Adrian Danek Hans H Jung Mariarosa A B Melone Luca Rampoldi Vania Broccoli Ruth H Walker

Neurological abnormalities associated with spiculated, "acanthocytic" red cells in blood have been summarized as neuroacanthocytosis. This is a heterogeneous group of conditions that can now be clearly subdivided on the basis of genetic discoveries. The core neuroacanthocytosis syndromes are autosomal recessive chorea-acanthocytosis (ChAc) and the X-linked McLeod syndrome (MLS). Huntington's di...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه ارومیه - دانشکده کشاورزی رضائیه 1393

ریحان(ocimum basilicum l.) از گیاهان دارویی تیره نعناع و سرشار از ترکیبات فنیل پروپانوئیدی است. در این تحقیق به منظور مطالعه تأثیر متیل جاسمونات بر بیان ژن های چاویکول-o-متیل ترنسفراز(cvomt) و سینامات چهار هیدروکسیلاز (c4h) (ژن های کلیدی دخیل در بیوسنتز فنیل پروپانوئیدها) و آنزیم های آنتی اکسیدانت آسکوربات پراکسیداز و گایاکول پراکسیداز در گیاه ریحان رقم کشکنی لولو، آزمایشی بر پایه طرح کاملاً تصا...

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