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Myotonic Dystrophy
Myotonic dystrophy (DM) is a multisystemic, inherited neuromuscular disorder and the most common form of adult-onset muscular dystrophy. It is…
Fragile X Syndrome
Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability and a leading single-gene cause of autism…
Trinucleotide Repeat Disorder
A trinucleotide repeat disorder is a type of genetic condition caused by an abnormal expansion of a sequence of three…
Polyalanine Tract Disorder
A polyalanine tract disorder refers to a group of genetic conditions caused by abnormal expansions of polyalanine (polyA) tracts within…
Hand–Foot–Genital Syndrome
Hand–Foot–Genital Syndrome is a rare genetic disorder characterized by congenital malformations affecting the limbs and the genitourinary tract. It belongs…
Polyglutamine Disease
Polyglutamine (polyQ) diseases are a group of inherited neurodegenerative disorders caused by abnormal expansions of CAG trinucleotide repeats in specific…
Polyglutamine Tract
Polyglutamine (polyQ) tracts are stretches of multiple glutamine amino acids repeated in sequence within proteins. These regions are encoded by…
Chorea
Chorea is a neurological movement disorder characterized by brief, irregular, involuntary movements that appear to flow from one muscle to…
TRIB3
TRIB3 (Tribbles Homolog 3), also known as NIPK or SKIP3, is a member of the Tribbles family of pseudokinases that…
TRIB2
TRIB2 (Tribbles Homolog 2) is a member of the Tribbles family of pseudokinases, which are evolutionarily conserved proteins that play…
DAXX
DAXX (Death Domain-Associated Protein) is a multifunctional nuclear protein that plays crucial roles in various cellular processes, including transcriptional regulation,…
QuikChange Site-Directed Mutagenesis Kit (Agilent Technologies)
The QuikChange Site-Directed Mutagenesis Kit is a molecular biology tool designed for the rapid and efficient introduction of specific nucleotide…
XPO1
XPO1 (Exportin 1), also known as CRM1 (Chromosome Region Maintenance 1), is a critical nuclear export receptor that belongs to…
DET1
DET1 (De-etiolated 1) is a highly conserved regulatory protein that plays crucial roles in both plants and animals, particularly in…
HA-Tag
The HA-tag is a widely used epitope tag derived from the human influenza hemagglutinin protein. It consists of nine amino…