Telomeres play an important role in protecting our chromosomes, but as we age, they decrease in length. In this blog we explore how and why telomeres shorten. Telomere structure Human telomeres are made up of thousands of repeats of the same DNA sequence (TTAGGG), bound by a special set of proteins called shelterin. They are […]
Since the COVID-19 global pandemic was declared by World Health Organization in March 2020 there has been a large amount of research conducted and published. Here we examine a couple of recent studies that have been conducted into telomeres and COVID-19. Short telomeres and COVID-19 A study conducted in Belgium, published in Aging, set out […]
To help raise awareness of rare disease dyskeratosis congenita, Julian’s mom Mayra has kindly shared his journey through 4 stem cell transplants this Rare Disease Day. At the age of 3, our son was diagnosed with a rare genetic disorder called, dyskeratosis congenita. We were really fortunate our search led us to the Jimmy Fund […]
In this blog we examine what short telomeres are and what short telomere syndromes can mean for certain individuals. What are telomeres for? Our chromosomes need to be protected to prevent damage, or them fusing with other chromosomes. Telomeres are the protective structures found on the end of chromosomes. They are made up of thousands […]
Please be aware of the RepeatDx holiday closure dates when shipping samples for telomere length testing. If you have any questions please contact us to discuss options. Holiday closure dates Wednesday 23 December Open Thursday 24 December Open Friday 25 December Closed Monday 28 December Closed Tuesday 29 December Open Wednesday 30 December Open Thursday […]
To mark Telomere Biology Disorder Month (TBD Month) this November, Mark is kindly sharing his journey of being diagnosed with dyskeratosis congenita, liver failure and undergoing a liver transplant. My journey with dyskeratosis congenita (DC) started in September 2016 when I was first diagnosed. I had become pretty sick in a short period of time, […]
This Telomere Biology Disorder Awareness Month (TBD Month) we have a guest blog from Colleen, Team Telomere President & Chair of Legacy. Colleen is kindly sharing her families’ story from unexpected diagnosis, to health care journeys, to the strength she has found in the Team Telomere community. If you would’ve told me 15 years ago […]
The results are in from our annual customer telomere testing satisfaction survey, here we take a look… Hearing from our customers is very important to us. We want to ensure that ordering a telomere test from us is as easy and straightforward as possible, as well as meeting the highest expectations in terms of turn […]
This Pulmonary Fibrosis Awareness Month we have a guest blog from Heather, who is kindly sharing her experience with IPF to help raise awareness. IPF diagnosis I was diagnosed with Idiopathic Pulmonary Fibrosis (IPF) in February, 2013. I was 43 years old. My father and grandfather both passed from IPF so I knew there was […]
This guest blog from the Canadian Pulmonary Fibrosis Foundation marks Pulmonary Fibrosis Awareness Month and explains the events and activities they have coordinated for September. Register now for fun and informative activities during Pulmonary Fibrosis Awareness Month Despite the pandemic, Pulmonary Fibrosis Awareness Month this September may be the best ever from the Canadian Pulmonary […]