نتایج جستجو برای: virb2 mutation

تعداد نتایج: 291443  

Journal: :journal of cellular and molecular anesthesia 0
akbar dorgalaleh department of hematology and blood transfusion, school of allied medicine, iran university of medical sciences, tehran shadi tabibian department of hematology and blood transfusion, school of allied medicine, iran university of medical sciences, tehran bijan varmaghani department of hematology and blood transfusion, school of allied medicine, iran university of medical sciences, tehran gholam hossein tamaddon department of hematology and blood transfusion, school of allied medicine, shiraz university of medical sciences, shiraz, iran hasan boustani department of hematology and blood transfusion, school of allied medicine, ilam university of medical sciences, ilam, iran

background: iran has a large group of patients with severe congenital factor xiii deficiency (fxiiid) and trp187arg mutation that is most disease causing mutation of fxiii in the world is only observed in southeast of iran with 352 patients with fxiiid. 743 patients with fxiiid was observed in 17 provinces of iran but tehran city with more than 12 million population has no any registered patien...

Journal: :middle east journal of cancer 0
hind dehbi genetics and molecular pathology laboratory, medical school of casablanca, hassan ii university, casablanca, morocco yaya kassogue genetics and molecular pathology laboratory, medical school of casablanca, hassan ii university, casablanca, morocco sanaa nasserddine genetics and molecular pathology laboratory, medical school of casablanca, hassan ii university, casablanca, morocco asma quessar department of onco-hematology, ibn rochd university hospital, casablanca, morocco sellama nadifi genetics and molecular pathology laboratory, medical school of casablanca, hassan ii university, casablanca, morocco

background :according to numerous studies, fms-like tyrosine kinase 3, internal tandem duplication, and the d835 mutation are associated with a poor prognostic clinical outcome in acute myeloid leukemia patients. detection of the fms-like tyrosine kinase 3 mutation in patients who present with normal karyotype acute myeloid leukemia helps in both the understanding of the disease and the treatme...

Haleh Akhavan Niaki, Mousa Ahmadpour Kachouri, Roya Farhadi, Yadollah Zahedpasha,

Background and Aim: Jaundice is a common disorder in neonates and one of the provable causes of glucose-6-phosphate dehydrogenase (G6PD) deficiency, some mutation types of which may be associated with severe neonatal icter. In this line, the present study has been conducted to compare G6PD mutations in incteric and non icteric neonates. Materials and Methods: This case-control study was imple...

Journal: :avicenna journal of medical biochemistry 0
rehana rehman department of biological and biomedical sciences, aga khan university, karachi, pakistan; department of biological and biomedical sciences, aga khan university, karachi, pakistan. tel: +92-2134864460, fax: +92-214934294 zehra jamil department of biological and biomedical sciences, aga khan university, karachi, pakistan syeda sadia fatima department of biological and biomedical sciences, aga khan university, karachi, pakistan faiza alam department of biological and biomedical sciences, aga khan university, karachi, pakistan

ژورنال: :gene, cell and tissue 0
xiuping yu health sciences center, louisiana state university, shreveport, usa robert j. matusik department of urologic surgery and vanderbilt prostate cancer center, vanderbilt university medical center, nashville, usa renjie jin department of urologic surgery and vanderbilt prostate cancer center, vanderbilt university medical center, nashville, usa; department of urologic surgery and vanderbilt prostate cancer center, vanderbilt university medical center, a1329, mcn, 1161 21st ave. south, nashville, tn 37232, usa. tel: +1-6159367849, fax: +1-6153432447

E Rezaei , H Dastsooz , H Faraji , J Manoochehri , Kh Sadeghi , M Fardaei , R Masoumi Dehshiri , S Mohammadi , T Moradi ,

Background Wilson disease (WD) is a rare autosomal recessive disorder, which leads to copper metabolism, due to mutations in ATP7B gene. The gene responsible for WD consists of 21 exons that span a genomic region of about 80 kb and encodes a copper transporting P-type ATPase (ATP7B), a protein consisting of 1465 amino acids. Identifying mutation in ATP7B gene is important to find carrier i...

بهار, بابک, توگه, غلام‌رضا, درگاهی, حسین, علی‌مقدم, کامران, عین‌الهی, ناهید, غفاری, سیدحمید‌اله, قوام‌زاده, اردشیر, موسوی, اسداله, نادعلی, فاطمه, چهاردولی, بهرام, کریم‌زاده, پریسا, ‌فردوسی, شیرین,

Background: JAK2 is a nonreceptor tyrosine kinase that plays a major role in myeloid disorders. This mutation is characterized by a G to T transverse at nucleotide 1849 in exon 12 of the JAK2 gene, located on the chromosome 9p, leading to a substitution of valine to phenylalanine at amino acid position 617 in the JAK2 protein. In this study we compared the amplification refractory mutation (ARM...

2009
Mingqun Lin Chunbin Zhang Kathryn Gibson Yasuko Rikihisa

Neorickettsia risticii is an obligate intracellular bacterium of the trematodes and mammals. Horses develop Potomac horse fever (PHF) when they ingest aquatic insects containing encysted N. risticii-infected trematodes. The complete genome sequence of N. risticii Illinois consists of a single circular chromosome of 879 977 bp and encodes 38 RNA species and 898 proteins. Although N. risticii has...

2018
Dong Zhou Fei-Jie Zhi Mao-Zhen Qi Fu-Rong Bai Guangdong Zhang Jun-Mei Li Huan Liu Hua-Tao Chen Peng-Fei Lin Ke-Qiong Tang Wei Liu Ya-Ping Jin Ai-Hua Wang

Brucella is an intracellular bacterium that causes the zoonosis brucellosis worldwide. Alveolar macrophages (AM) constitute the main cell target of inhaled Brucella. Brucella thwarts immune surveillance and evokes endoplasmic reticulum (ER) stress to replicate in macrophages via virulence factors. The GntR regulators family was concentrated as an important virulence factor in controlling virule...

ذاکر کیش, مهرنوش, سمرباف زاده, علیرضا, مروج آل‌علی, ارمغان, مولا, کریم,

Background: Behcet’s disease (BD) is a multisystemic inflammatory disease with unknown origin characterized by recurrent oral aphtous ulcers, genital, ocular and skin lesions. A single point mutation 1691G to A in the factor V gene increases the risk of venous thrombosis. This study designed to determine factor V Leiden mutation in Behcet’s disease, and to find out it's relationship with the cl...

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