نتایج جستجو برای: triplication

تعداد نتایج: 451  

2012
Blake Byers Hsiao-lu Lee Renee Reijo Pera

Our understanding of the underlying molecular mechanism of Parkinson's disease (PD) is hampered by a lack of access to affected human dopaminergic (DA) neurons on which to base experimental research. Fortunately, the recent development of a PD disease model using induced pluripotent stem cells (iPSCs) provides access to cell types that were previously unobtainable in sufficient quantity or qual...

Journal: :ACM Transactions on Sensor Networks 2023

Energy efficiency, real-time response, and data transmission reliability are important objectives during networked systems design. This paper aims to develop an efficient task mapping scheme balance these but conflicting objectives. To achieve this goal, tasks triplicated enhance mapped on the wireless nodes of with Dynamic Voltage Frequency Scaling (DVFS) capabilities reduce energy consumption...

Journal: :iranian journal of public health 0
sa alemohammad dd farhud m hooshmand m sanati p derakhshandeh-peykar sj imam

a 9 bp deletion between cytochrome oxidase subunit ii and trna lys genes in mitochondrial dna, has proven to be an extremely informative marker for tracing population history. using the pcr-page and pcr-sscp techniques in this study, 152 dna samples collected from iranian populations were screened for the 9 bp deletion. no deletion was observed. a length polymorphism, most probably a 9 bp tripl...

Journal: :Molecular biology and evolution 2012
Dries Vekemans Sebastian Proost Kevin Vanneste Heleen Coenen Tom Viaene Philip Ruelens Steven Maere Yves Van de Peer Koen Geuten

Comparative genome biology has unveiled the polyploid origin of all angiosperms and the role of recurrent polyploidization in the amplification of gene families and the structuring of genomes. Which species share certain ancient polyploidy events, and which do not, is ill defined because of the limited number of sequenced genomes and transcriptomes and their uneven phylogenetic distribution. Pr...

2006
María Paulina Nava Bertha Ibarra María Teresa Magaña María de la Luz Chávez F. Javier Perea

The aim of this study was to determine the frequency of α-globin gene mutations in three groups of Mexican unrelated individuals. The first two groups were normal and sickle cell trait individuals from the Costa Chica region, a place with a 12.8% frequency of HbS carriers, and the third group comprised of Mexican mestizo patients with β-thalassemia. We searched for −α and −α α-thalassemia delet...

Journal: :journal of dentomaxillofacil radiology, pathology and surgery 0
anousheh rashed mohassel department of pedodontics, faculty of dentistry, birjand university of medical sciences, birjand, iran. samir zahedpasha department of endodontics, faculty of dentistry, birjand university of medical sciences, birjand, iran. mahtab hamzeh department of pediatric denti stry, guilan university of medical sciences, rasht, iran.

dental anomalies are rare findings that may affect development of occlusion and early intervention may be required. here, a case of multiple anomalies in primary and perma nent dentitions is reported. the patient referred to the dental center with the chief complaint of multiple tooth decay. in the oral examination, the rare case of triplica tion between the right geminated man-dibular a and ri...

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