نتایج جستجو برای: yq deletions

تعداد نتایج: 19460  

علی بخشی, رضا , زربخش, بهناز , زینلی, سیروس , کریمی پور, مرتضی , کیانی شیرازی, رویا ,

Background and Aim:-thalassemia is the most common inherited disorder of hemoglobin (Hb) synthesis in the world. Alpha thalassemia most frequently results from the loss of one (- ) or both (- -) of the duplicated  genes () on chromosome 16. Carriers of deletional forms of -thalassemia (-/- /-, or --/) are clinically normal but have a mild hypochromic, microcytic anemia. C...

Ataxia-Telangiectasia (AT) is a rare human neurodegenerative autosomal recessive multisystem disease that is characterized by a wide range of features including, progressive cerebellar ataxia with onset during infancy, occulocutaneous telangiectasia, susceptibility to neoplasia, occulomotor disturbances, chromosomal instability and growth and developmental abnormalities. Mitochondrial DNA (mtDN...

Journal: :avicenna journal of medical biotechnology 0

background: limited resources for adult stem cells necessitate their in vitro culture prior to clinical use. investigating mitochondrial dna (mtdna) and telomere shortening has proved to be important indications of stem cell validity. this study was designed to investigate these indicators in multiple passages of three adult stem cell lines which were produced in our stem cell laboratory. metho...

Journal: :Journal of Assisted Reproduction and Genetics 2012

Journal: :I. J. Bifurcation and Chaos 2001
Tao Yang Leon O. Chua

In this paper we study the local activity, local passivity and edge of chaos of continuous-time reaction–diffusion cellular nonlinear networks (CNN) with one-port first-order, one-port secondorder, two-port second-order, two-port third-order and three-port third-order cells. We prove that the local passive regions determined by cell impedance ZQ(s) and cell admittance YQ(s) for firstand second-...

Journal: :Annales de biologie clinique 2014
Wajih Hammami Olfa Kilani Mariem Ben Khelifa Wiem Ayed Sonia Abdelhak Abderrezzak Bouzouita Fethi Zhioua Ahlem Amouri

Yq microdeletions are the leading genetic cause of male infertility and its detection in clinically relevant for appropriate genetic counseling. The objective of this study was to determine the frequency of Y microdeletion in a group of Tunisian infertile men and to compare the prevalence of these abnormalities with other countries and other Tunisian reported series. Totally, 105 Tunisian idiop...

Journal: :Chemosphere 2010
Faizan Haider Khan Panneer Ganesan Sudhir Kumar

Recent studies have shown Y chromosome microdeletions associated with male infertility. The factors responsible for Y chromosome microdeletions in spermatozoa remain unresolved. However, the environmental pollutants are known to damage DNA in differentiating and maturing germ cells in the male reproductive tract. Therefore, the aim of this study was to investigate the effects of seminal hexachl...

Journal: :CoRR 2017
Xiaofan Xu Shaofang Hong Yongchao Xu

Abstract. Determining deep holes is an important topic in decoding Reed-Solomon codes. Cheng and Murray, Li and Wan, Wu and Hong investigated the error distance of generalized Reed-Solomon codes. Recently, Zhang and Wan explored the deep holes of projective Reed-Solomon codes. Let l ≥ 1 be an integer and a1, . . . , al be arbitrarily given l distinct elements of the finite field Fq of q element...

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