نتایج جستجو برای: memory de duplication

تعداد نتایج: 1802836  

2008
R. de Lima Rodrigues Arvind Narayan Vaidya

R. de Lima Rodrigues Unidade Acadêmica de Educação Universidade Federal de Campina Grande, Cuité PB, CEP 58.175-000Brazil Centro Brasileiro de Pesquisas F́ısicas (CBPF) Rua Dr. Xavier Sigaud, 150, CEP 22290-180, Rio de Janeiro, RJ, Brazil Jambunatha Jayaraman (In memory) Departamento de F́ısica (CCEN), Universidade Federal da Paráıba, Campus I, João Pessoa-PB, CEP 58.059-970, Brazil Arvind Naraya...

Journal: :Genetics 2016
Andrew P Morgan J Matthew Holt Rachel C McMullan Timothy A Bell Amelia M-F Clayshulte John P Didion Liran Yadgary David Thybert Duncan T Odom Paul Flicek Leonard McMillan Fernando Pardo-Manuel de Villena

Gene duplication and loss are major sources of genetic polymorphism in populations, and are important forces shaping the evolution of genome content and organization. We have reconstructed the origin and history of a 127-kbp segmental duplication, R2d, in the house mouse (Mus musculus). R2d contains a single protein-coding gene, Cwc22 De novo assembly of both the ancestral (R2d1) and the derive...

Journal: :Journal of medical genetics 2002
M M van Haelst H J F M M Eussen F Visscher J L M de Ruijter S L S Drop D Lindhout C H Wouters L C P Govaerts

Partial duplication of the long arm of chromosome 1 has been described in more than 200 patients. In most of these cases, the duplication is the result of an unbalanced segregation of a parental balanced translocation. Patients with duplications of 1q are therefore monosomic for the other chromosomal material involved in the translocation. The phenotypic result of such chromosomal abnormalities...

2017
Tao Li Zhao-jing Zhang Xin Ma Xue Lv Hai Xiao Qian-nan Guo Hong-yan Liu Hong-dan Wang Dong Wu Gui-yu Lou Xin Wang Chao-yang Zhang Shi-xiu Liao

BACKGROUND Patients with Duchenne muscular dystrophy (DMD) usually have severe and fatal symptoms. At present, there is no effective treatment for DMD, thus it is very important to avoid the birth of children with DMD by effective prenatal diagnosis. We identified a de novo DMD gene mutation in a Chinese family, and make a prenatal diagnosis. METHODS First, multiplex ligation-dependent probe ...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه اصفهان - دانشکده ادبیات و زبانهای خارجی 1392

selon les pédagogues, la culture étant un élément très important dans le processus de lapprentissage de langue étrangère et la maîtrise de la compétence linguistique requiert celle de la compétence culturelle. la littérature dun pays est comme un miroir qui reflète bon nombre daspects culturels, cest pourquoi avec le choix dun texte littéraire convenable, lenseignant peut assurer à la fois lapp...

2009
Ashok Anand Steven Kappes Aditya Akella Suman Nath

We show how to build cheap and large CAMs, or CLAMs, using flash memory. These CLAMs are targeted at an emerging class of networking applications that require massive indexes running into a hundred GB or more, with items been inserted, updated and looked up at a rapid rate. Examples of such applications include WAN optimizers, data de-duplication, network monitoring, and traffic analyzers. For ...

Journal: :archives of clinical infectious diseases 0
mohammad naderi infectious diseases and tropical medicine research center, zahedan university of medical sciences, zahedan, ir iran mohammad hashemi department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran; department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran. tel: +98-5433295740, fax: +98-5433425728 shadi amininia department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran maryam rezaei department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran mohsen taheri genetic of non-communicable diseases research center, school of medicine, zahedan university of medical sciences, zahedan, ir iran

conclusions in conclusion, chit1 24 bp duplication might not be a candidate gene for susceptibility to ptb. larger studies are necessary to confirm these findings in various populations. results homozygous wild type, heterozygous and homozygous mutant frequencies of chit1 24 bp duplication polymorphism were 43.9%, 43.9% and 12.2% in controls and 42.8%, 45.1% and 12.1% in ptb patients. we found ...

Journal: :iranian journal of basic medical sciences 0
zahra vojdani laboratory for stem cell research, anatomy department, shiraz university of medical sciences, shiraz, iran ali babaei laboratory for stem cell research, anatomy department, shiraz university of medical sciences, shiraz, iran attiyeh vasaghi laboratory for stem cell research, anatomy department, shiraz university of medical sciences, shiraz, iran mojtaba habibagahi immunology department, shiraz university of medical sciences, shiraz, iran tahereh talaei-khozani laboratory for stem cell research, anatomy department, shiraz university of medical sciences, shiraz, iran

objective(s): umbilical cord blood is a good source of the mesenchymal stem cells that can be banked, expanded and used in regenerative medicine.  the objective of this study was to test whether amniotic membrane extract, as a rich source of growth factors such as basic-fibroblast growth factor, can promote the proliferation potential of the umbilical cord mesenchymal stem cells. materials and ...

Journal: :Journal of speech, language, and hearing research : JSLHR 2014
Shiri Oren Charlene Willerton Jeff Small

PURPOSE This article reports on a systematic review and meta-analysis of the effects of spaced retrieval training (SRT) on semantic memory in people with Alzheimer’s disease (AD) or related disorder. METHOD An initial systematic database search identified 454 potential studies. After screening and de-duplication, 35 studies that used SRT with the population of interest remained. The authors u...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تبریز 1390

la robinsonnade est un thème littéraire qui provient du nom de robinson, le personnage créé par lauteur anglais daniel defoe, au xviii e siècle, dans son œuvre intitulée, la vie et les aventures de robinson crusoë, (1719). une robinsonnade comporte un double sens : lun qui est une indication de fiction et lautre comme un commentaire, car pour lécrivain dune robinsonnade, il y a une double tâch...

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