Dedicated to the acceptance, medical treatment, & legal protection of individuals in the process of correcting the misalignment of their anatomical sex, & supporting their transition into society.

 
TS-Si Science Access/Genetics and the Genome
Defining The Characteristics And Treatment Options For XXYY Syndrome
TS-Si News Service
Wednesday, 27 August 2008
Sacramento, CA, USA. Researchers are closer to understanding XXYY Syndrome, a rare genetic anomaly in which males have two "X" and two "Y" chromosomes. A research team conducted the largest study to date describing the medical and psychological characteristics of XXYY, developing recommendations for men and boys with the disorder.
The study of XXYY Syndrome illustrates the importance of developing a reliable observation baseline. Developmental biologists and geneticists study the underlying mechanisms that guide human development. A clear understanding of the consequences when events do not follow an expected pattern can provide important information on which to base prevention and/or treatment options.

A new look at XXYY sy
Classic Discoveries: Gene Silencing And The Discovery Of RNA Interference
TS-Si News Service
Sunday, 17 August 2008
Washington, DC, USA. A fundamental mechanism inhibits gene expression during translation or hinders the transcription of specific genes. Called RNA interference (RNAi), it targets RNA that is significant for some forms of our innate immune response and plays a key role in regulating development and genome maintenance.
RNAi has a selective and robust effect on gene expression, making it an essential research tool in cell culture and living organisms. The introduction of synthetic dsRNA into cells can induce the suppression of specific genes. Large-scale screens that systematically shut down each gene in the cell use RNAi to help identify the components necessary for a particular cellular process or an event su
The Mouse: Important Model Organism Receives Increased Attention
TS-Si News Service
Wednesday, 13 August 2008
New Haven, CT, USA. The mouse is commonly used as a model organism in biomedical research. For example, a great deal of work has been done to figure out what a particular gene does in an organism. Scientists can replace the subject gene with a non-functional version and breed the individual, then look at the offspring to obseve the effects.
As a result of this and other techniques, the mouse has become a crucial part of scientific history through its contributions in understanding human genetics and disease. In a new review, genetics researchers from Yale University School of Medicine and Fudan University School of Life Sciences discuss the history and future of this important model organism.

The exp
Next Generation Data Visualization Tool For Exploring The Genome
TS-Si News Service
Monday, 04 August 2008
Cambridge, MA, USA. The genome contains a lot of data that has to be collected, cleaned, normalized, processed, and analyzed in a manner. This has to be done in a manner that enhances understanding and can lead to new insights. With increasing computer power available, data visualization has come into its own.
Scientists and others have communicated using visual media since the dawn of humanity. However, the advent of serious attention to the genome has resulted in the collection of and vast quantities of new data. Researchers collect vast amounts of diverse genomic data with ever-increasing speed, but effective ways to visualize these data in an integrated manner have lagged behind the ability to generate th
Repairing Broken DNA And The Consequences If We Can't
TS-Si News Service
Sunday, 27 July 2008
San Antonio, TX, USA. Repair mechanisms exist throughout the human body, but what happens when DNA is broken? The genome itself is the source of our body and any unrepaired — or poorly repaired — breaks can have profound consequences. The result can be anomalous birth conditions and often-fatal diseases.
Generally speaking, broken pieces of DNA in our cells reunite as they are repaired. These pieces tether together following a quick and precise [N1] process of mutual identification. A suppressor gene called ATM choreographs this fast-paced, but reliable, reassembly operation. But happens when an important mechanism for repair is itself broken?

Saccharomyces cerevisiae ATM orthologue suppresses break-
Separator
Global Warning: Opinion by Lisa Jain Thompson 
 
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