Knockout Mouse Catalog | Cyagen APAC
Weekly Gene Ophthalmology
Genetic Factors of Eye Disease: Retinitis Pigmentosa (RP) & the RHO Gene
Genes play a significant role in the pathogenesis of eye diseases, some of which are highly prevalent in children and adults. Read More ›
Weekly Gene
Targeting BBS5 in Bardet-Biedl syndrome (BBS)
Bardet-Biedl Syndrome (BBS) is a rare genetic disorder with highly variable symptoms which may include retinal degeneration. Read More ›
Weekly Gene
[Weekly Gene] The Secret of YBX2's Regulatory Mechanisms
Although the gene YBX2 is not the direct cause of cancer, it seems to be inextricably linked to cancer, and the latest research shows that high YBX2 expression is unfavorable in prognosis of endometrial cancer. Read More ›
Weekly Gene
[Weekly Gene]—The 'Culprit' of Osteoarthritis - ADAMTS5
On the 21st anniversary of the discovery of ADAMTS-5, this article looks at its deleterious effects in development of Osteoarthritis (OA). Read More ›
Weekly Gene
[Weekly Gene]—Will the MARCHF2 Gene be the Next Research Hotspot?
MARCH2 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC Read More ›
Weekly Gene
[Weekly Gene]—Targeting INPP5E in Rare Disease
INPP5E (Inositol Polyphosphate-5-Phosphatase E) is a Protein Coding gene. Diseases associated with INPP5E include Joubert Syndrome 1 and Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis (MORM) Syndrome. Read More ›
Weekly Gene
[Weekly Gene]—Targeting STAT3 in Rare Disease
The STAT3 (Signal Transducer And Activator Of Transcription 3) gene is part of the STAT gene family. Read More ›
Weekly Gene
[Weekly Gene]—Research progress of gene UTS2
Urotensin II (UTS2/UII) is a potent vasoconstrictor peptide, which signals through a G-protein coupled receptor (GPCR) known as GPR14 or urotensin receptor (UTR). Read More ›
Weekly Gene
Parkinson's Disease (PD) and the FGF20 Gene
Parkinson's disease (PD) is a neurodegenerative disorder that predominantly affects dopamine-producing (“dopaminergic”) neurons in a specific area of the brain, called the substantia nigra. Read More ›
Weekly Gene
The "Culprit" Of the Rare Diseases MCTD/OPMD - HNRNPC
In this article, we review the hottest oncogene HNRNPC, hoping to give you insights on its role in rare disease development as a therapeutic target in MCTD research. Read More ›