نتایج جستجو برای: complete duplication

تعداد نتایج: 378964  

Background and Objective: The clinical outcomes and treatment options for acute myeloid leukemia (AML) patients are highly dependent upon molecular markers. In this study, Wilms tumor (WT1) (exons 7 and 9) mutations, SNP rs16754, and WT1 expression levels in 130 random AML patients were screened; FMs-like tyrosine kinase-3 internal tandem duplication (FLT3-ITD), nucleophosmin (NPM1), and CCAAT/...

Journal: :Genomics 2006
Stephen D Eastman Tim H-P Chen Matthias M Falk Tamra C Mendelson M Kathryn Iovine

Gap junctions, composed of connexin proteins in chordates, are the most ubiquitous form of intercellular communication. Complete connexin gene families have been identified from human (20) and mouse (19), revealing significant diversity in gap junction channels. We searched current databases and identified 37 putative zebrafish connexin genes, almost twice the number found in mammals. Phylogene...

Journal: :Journal of computational biology : a journal of computational molecular cell biology 2009
Jin Jun Paul Ryvkin Edward Hemphill Ion I. Mandoiu Craig E. Nelson

Gene duplication has long been recognized as a major force in genome evolution and has recently been recognized as an important source of individual variation. For many years, the origin of functional gene duplicates was assumed to be whole or partial genome duplication events, but recently retrotransposition has also been shown to contribute new functional protein coding genes and siRNA's. In ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Xiang Gao Michael Lynch

Duplication of genomic segments provides a primary resource for the origin of evolutionary novelties. However, most previous studies have focused on duplications of complete protein-coding genes, whereas little is known about the significance of duplication segments that are entirely internal to genes. Our examination of six fully sequenced genomes reveals that internal duplications of gene seg...

Journal: :Computer and Information Science 2012
Gary Cantrell David A. Dampier Yoginder S. Dandass Nan Niu A. Chris Bogen

The digital forensic process as traditionally laid out begins with the collection, duplication, and authentication of every piece of digital media prior to examination. These first three phases of the digital forensic process are by far the most costly. However, complete forensic duplication is standard practice among digital forensic laboratories. The time it takes to complete these stages is ...

2011
Masashi Takemura Kayo Yoshida Keiichirou Morimura

Esophageal duplication cyst is a rare congenital anomaly. They can be associated with other congenital anomalies, such as spinal abnormalities, and tracheoesophageal fistulas. In adults, almost of the patients with esophageal duplication cyst is asymptomatic and accidentally diagnosed by chest X-ray or computed tomography. However, cysts may become symptomatic owing to complications such as eso...

2017

The urethral duplication or supernumerary urethra or called accessory urethra is an exceptional malformative uropathy of interest mainly to the boy [1]. It is defined by the juxtaposition of 2 or more channels with smooth muscular structure with a mucosal coating of excreto-urinary type [2]. It can be complete or incomplete [3]. It occurs preferentially in the sagittal plane but also in the fro...

Journal: :Journal of medical genetics 1996
B R Haddad A E Lin H Wyandt A Milunsky

We report on a father and daughter with a partial 9p duplication, dup(9)(p22p24). Their phenotype, albeit mild, is characteristic of partial trisomy 9p. Fluorescence in situ hybridisation (FISH) was used to characterise further and confirm the G banding finding. This is the first reported instance of trisomy 9p occurring in two successive generations. The duplicated segment in these two patient...

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