نتایج جستجو برای: gene duplication

تعداد نتایج: 1147273  

2014
Alex N. Nguyen Ba Bob Strome Jun Jie Hua Jonathan Desmond Isabelle Gagnon-Arsenault Eric L. Weiss Christian R. Landry Alan M. Moses

Gene duplication is an important evolutionary mechanism that can result in functional divergence in paralogs due to neo-functionalization or sub-functionalization. Consistent with functional divergence after gene duplication, recent studies have shown accelerated evolution in retained paralogs. However, little is known in general about the impact of this accelerated evolution on the molecular f...

Journal: :iranian journal of science and technology (sciences) 2005
j. raheb

the combustion of sulfur-rich fossil fuels leads to the release of acid rain-causing sulfurdioxide into the environment. the aim of this study was to enhance the efficiency of biodesulfurizationusing pseudomonas aeruginosa through the duplication of the dsz cluster in this organism. one copy ofthe dsz cluster was inserted by a tri-parental mating method into the chromosome of pseudomonasaerugin...

Journal: :Trends in genetics : TIG 2005
Steven Lockton Brandon S Gaut

Genome duplication is a powerful evolutionary force and is arguably most prominent in plants, where several ancient whole-genome duplication events have been documented. Models of gene evolution predict that functional divergence between duplicates (subfunctionalization) is caused by the loss of regulatory elements. Studies of conserved non-coding sequences (CNSs), which are putative regulatory...

Journal: :Trends in genetics : TIG 2001
J S Taylor Y Van de Peer A Meyer

What are the evolutionary consequences of gene duplication? One answer is speciation, according to a model initially called Reciprocal Silencing and recently expanded and renamed Divergent Resolution. This model shows how the loss of different copies of a duplicated gene in allopatric populations (divergent resolution) can promote speciation by genetically isolating these populations should the...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2011
Jihun Lee Michael Blaber

The majority of protein architectures exhibit elements of structural symmetry, and "gene duplication and fusion" is the evolutionary mechanism generally hypothesized to be responsible for their emergence from simple peptide motifs. Despite the central importance of the gene duplication and fusion hypothesis, experimental support for a plausible evolutionary pathway for a specific protein archit...

Journal: :Genetics 2005
Ambro van Hoof

Gene duplication is often cited as a potential mechanism for the evolution of new traits, but this hypothesis has not been thoroughly tested experimentally. A classical model of gene duplication states that after gene duplication one copy of the gene preserves the ancestral function, while the other copy is free to evolve a new function. In an alternative duplication, divergence, and complement...

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: :Genome research 2001
A L Hughes J da Silva R Friedman

The fact that there are four homeobox (Hox) clusters in most vertebrates but only one in invertebrates is often cited as evidence for the hypothesis that two rounds of genome duplication by polyploidization occurred early in vertebrate history. In addition, it has been observed in humans and other mammals that numerous gene families include paralogs on two or more of the four Hox-bearing chromo...

Journal: :Neuromuscular Disorders 2021

This work describes a family with Duchenne muscular dystrophy (DMD) rare case of symptomatic pregnant woman. The main aim was to perform prenatal molecular diagnosis provide genetic counseling. secondary suggest the mechanisms causing complex structural variant (cxSV) identified. To accomplish this, we used multi-technique algorithm including segregation analysis, Multiplex Ligation-dependent P...

Journal: : 2021

Objective: Dystrophinopathies are the most frequently researched neuromuscular disease group due to their characteristic and diverse clinical genetic spectrum. This study aims evaluate deletion duplication profile of dystrophin gene in Turkey by investigating data from a tertiary center. Material Methods: Dystrophin MLPA microarray results 53 patients, 49 with dystrophinopathy 4 neurogenetic sy...

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