Retrotransposons, which used to be considered as “junk DNA”, have begun to reveal their immense value to genome evolution and human biology due to recent studies. They consist of at least ~45% of the human genome and are more or less the same in other mammalian genomes. Retrotransposon elements (REs) are known to affect the human genome through many different mechanisms, such as generating insertion mutations, genomic instability, and alteration in gene expression. Previous studies have suggested several RE subfamilies, such as Alu, L1, SVA and LTR, are currently active in the human genome, and they are an important source of genetic diversity between human and other primates, as well as among humans. Although several groups had used Retrot...
RNA polymerases initiate transcription at DNA sequences called promoters. In bacteria, the best cons...
Polycystic Kidney Disease (PKD) is the most common genetic cause of kidney failure in children and a...
The success of human gene therapy - the treatment of hereditary or acquired diseases with a genetic ...
Speciation and evolution of species are two of the most exciting topics in biology. Radiations, with...
An integral part of evolution, the formation of species, is less well understood than other areas of...
Sequence comparison is an essential tool in modern biology. It is used to identify homologous region...
The main focus of my PhD has been the analysis of rare and common variants in genetic susceptibility...
Idiopathic nephrotic syndrome (INS) is classified in children according to response to initial corti...
The advent of massively-parallel next-generation sequencing (NGS) methods has provided researchers w...
Background: Vestibular schwannoma (VS) is a benign intracranial neoplasm associated with reduced qua...
Multiple myeloma (MM) is a haematological malignancy characterised by the uncontrolled clonal prolif...
Human African trypanosomiasis (HAT), also known as sleeping sickness, has been a major health proble...
Recent investigations have suggested the feasibility of establishing a species identification system...
Zimmermann-Laband syndrome (ZLS; MIM135500) is a rare developmental disorder characterized by facia...
The explosion of genomics permits investigations into the origin and early evolution of the Metazoa...
RNA polymerases initiate transcription at DNA sequences called promoters. In bacteria, the best cons...
Polycystic Kidney Disease (PKD) is the most common genetic cause of kidney failure in children and a...
The success of human gene therapy - the treatment of hereditary or acquired diseases with a genetic ...
Speciation and evolution of species are two of the most exciting topics in biology. Radiations, with...
An integral part of evolution, the formation of species, is less well understood than other areas of...
Sequence comparison is an essential tool in modern biology. It is used to identify homologous region...
The main focus of my PhD has been the analysis of rare and common variants in genetic susceptibility...
Idiopathic nephrotic syndrome (INS) is classified in children according to response to initial corti...
The advent of massively-parallel next-generation sequencing (NGS) methods has provided researchers w...
Background: Vestibular schwannoma (VS) is a benign intracranial neoplasm associated with reduced qua...
Multiple myeloma (MM) is a haematological malignancy characterised by the uncontrolled clonal prolif...
Human African trypanosomiasis (HAT), also known as sleeping sickness, has been a major health proble...
Recent investigations have suggested the feasibility of establishing a species identification system...
Zimmermann-Laband syndrome (ZLS; MIM135500) is a rare developmental disorder characterized by facia...
The explosion of genomics permits investigations into the origin and early evolution of the Metazoa...
RNA polymerases initiate transcription at DNA sequences called promoters. In bacteria, the best cons...
Polycystic Kidney Disease (PKD) is the most common genetic cause of kidney failure in children and a...
The success of human gene therapy - the treatment of hereditary or acquired diseases with a genetic ...