Knockout Mouse Catalog | Cyagen APAC
Rare Diseases
Genetic Disorder: Cystic Fibrosis, The Salty Kiss
Cystic fibrosis (CF) is an inherited disease that can cause severe damage to the lungs, digestive system and other organs in the body. Read More ›
Rare Diseases
Amyotrophic Lateral Sclerosis (ALS): A Rare Disease More Common in EU&US
Amyotrophic lateral sclerosis (ALS) is designated as a rare disease due to its low prevalence in the general population, which also fluctuates among different regional groups. Read More ›
Rare Diseases
Amyotrophic Lateral Sclerosis (ALS) - A Fatal Disease Racing Against Time
Amyotrophic lateral sclerosis (ALS), also known as motor neurone disease (MND), is a neurodegenerative disease that results in the progressive loss of motor neurons that control voluntary muscles. Read More ›
Research Trend Rare Diseases
Novel Insights into the Animal Models of Huntington's Disease (HD)
In this article, we will further demystify HD, introducing its causative genes, other treatments, and the application of related animal models. Read More ›
Rare Diseases
What is Huntington's Disease?
Huntington's disease (HD), also known as Huntington's chorea, is a neurodegenerative disease that has a 50% probability of being inherited by children of people living with HD. Read More ›
Rare Diseases Cyagen Newsletter
SYNGAP1-Related Intellectual Disability (MRD5)
Cyagen assists in the research of rare diseases and provides various mouse/rat models, including the SYNGAP1-related rodent animal models. This article focuses on the gene SYNGAP1 and rare disease MRD5, aiming to help interested researchers continue to build on scientific literature and knowledge. Read More ›
Rare Diseases
Rare Diseases Caused by the CEP290 Gene
Cyagen assists in the research of rare diseases and provides various mouse/rat models, including the Cep290 knockout mouse. This article focuses on the gene CEP290 and its related rare diseases, aiming to help interested researchers continue to build on scientific literature and knowledge. Read More ›