نتایج جستجو برای: carrier detection

تعداد نتایج: 633978  

2015
Anandteerth S Mathad Mrinal Sarvagya

In this paper, the performance of the carrier sense multiple access with collision avoidance (CSMA/CA) protocol at MAC layer with sensing errors at physical layer is investigated. Here the sensing errors are captured by modifying the Markov chain model widely used for the CSMA/CA analysis called Bianchi’s model. We investigate the throughput as a function of carrier sensing error probabilities:...

Journal: :JDCTA 2010
Ming-Hour Yang

To diagnose the vulnerabilities of target system using a remote penetration test approach needs to avoid the modification of the security configuration of the target network. So the carrier of test codes needs to hide from the IDS filter out of our penetrating test codes. Hence, we proposed a polymorphic carrier which carries encrypted test codes and diversified decrypters, and, the proposed ca...

Akbar Dorgalaleh, Farhad Zaker, Hasan Mollanoori, Hojat Shahraki, Majid Fathi, Maryam Daneshi, Omolbanin Sargazi-Aval, Shadi Tabibian, Shahram Teimourian,

Background: Congenital factor XIII (FXIII) deficiency is one of the rarest bleeding disorders with a prevalence of one per 2 million in the general population. The disorder is accompanied by a high rate of life-threatening bleeding. Due to normal results of routine coagulation tests, diagnosis of the disorder is challenging, but molecular methods can be used for precise diagnosis. Direct mutati...

Journal: :تحقیقات دامپزشکی 0
سعید زیبائی موسسه تحقیقات واکسن و سرم سازی رازی شعبه شمال شرق، بخش تحقیقات دامپزشکی و بیوتکنولوژی، مشهد–ایران صمد رضائی دانش آموخته گروه بیوشیمی، دانشگاه پیام نور مشهد، مشهد –ایران محمد رشتی باف بخش بررسی ها، اداره کل دامپزشکی استان خراسان رضوی، مشهد –ایران

background: foot -and- mouth disease (fmd) is endemic in iran. molecular techniques for diagnosis of persistent infection or carrier animals have shown a potential ability to improve the detection of a low genome copy number in samples. objectives: the purpose of this study is to evaluate the frequency of foot and mouth disease viral carriers in slaughtered sheep in mashhad industrial abattoir ...

Objective(s): Iran is considered as one of the high-prevalence areas for β-thalassemia with a rate of about 10% carrier frequency. Molecular diagnosis of the disease is performed both by direct sequencing and indirectly by the use of polymorphic markers present in the beta globin gene cluster. However, to date there is no reliable information on the application of the markers in the Iranian pop...

Journal: :Journal of the American Academy of Audiology 2009
Brian C J Moore Vinay

BACKGROUND A dead region is a region in the cochlea where the inner hair cells and/or neurons are functioning very poorly, if at all. We have shown that, for people with sensorineural hearing loss, thresholds for detecting sinusoidal amplitude modulation (AM) of a sinusoidal carrier were lower for ears with high-frequency dead regions, as diagnosed using the threshold-equalizing noise test, cal...

2005
Stanislas Boutoille Serge Reboul Mohammed Benjelloun

In a GPS receiver, the goal of the signal tracking is to synchronize local generated code and carrier with the received signal. After a step of acquisition, the receiver tracks the shifting of the local code provoked by the movements of the receiver and satellites. In the future evolution of the GPS, the system will have several carrier frequencies, then it will be possible to have several trac...

Journal: :The Journal of the Acoustical Society of America 2005
Stéphane Lacher-Fougère Laurent Demany

Thresholds for detecting interaural phase differences (IPDs) in sinusoidally amplitude-modulated pure tones were measured in seven normal-hearing listeners and nine listeners with bilaterally symmetric hearing losses of cochlear origin. The IPDs were imposed either on the carrier signal alone-not the amplitude modulation-or vice versa. The carrier frequency was 250, 500, or 1000 Hz, the modulat...

A. Shakoori E. Darabi M.R. Noori Daloii N. Ebadi S. Mehrabi

The aim of this study was to examine the feasibility of using an economic and practical method in order to perform non-invasive prenatal testing of thalassemia as a sing gene disorder.Sixteen (16) pregnant mothers in the 11th week of pregnancy who were referred for prenatal diagnosis of thalassemia were selected. The parents had one of IVSII-1, IVSI-5 or FR codon 8/9 mutations. Enrichment of cf...

Journal: :Blood 1988
E R Fearon D B Kohn J A Winkelstein B Vogelstein R M Blaese

The Wiskott-Aldrich syndrome (WAS) is an X-linked recessive disease characterized by immunodeficiency and severe thrombocytopenia in affected males, but no demonstrable clinical abnormalities in carrier females. Through analysis of the methylation patterns of X-linked genes that display restriction fragment length polymorphisms (RFLPs), we studied the pattern of X-chromosome inactivation in var...

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