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A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Semecarpus anacardium leaf extracts may offer safe, effective cancer treatment alternatives.

A 69-year-old man with sinus infection and fainting spells was diagnosed with a rare kidney disease, treated with steroids and a specific drug, which improved his condition.

Snakin-Z from jujube fruits may help treat Alzheimer's due to its enzyme inhibition and antioxidant properties.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

Increasing TSPO in the brain reduces anxiety and depression.

Trichohyalin is a protein in hair follicles that helps form hair filaments.

A new gene mutation causes insulin resistance in a girl and her mother.

Researchers found a non-functional sheep keratin gene due to mutations.

SLE affects lungs and kidneys similarly due to immune complexes.

Cerebronal® may help improve certain brain health markers.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Transglutaminases work through a ping-pong mechanism, and human plasma and platelet transglutaminases have similar catalytic subunits.

Anti-Ku antibodies are linked to unique symptoms and may involve autophagy issues.

Sex and sex hormones can affect brain inflammation in Parkinson's disease, with male mice being more affected and female mice showing a protective effect.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

A new gene causes hairlessness and skin cysts in rats.

Arg1+ macrophages may play a role in Alopecia Areata, offering new treatment targets.

Manganese levels in hair may be linked to multiple sclerosis.

Excessive putrescine causes hair loss in transgenic mice by disrupting hair follicle development.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

A scalp biopsy revealed systemic amyloidosis in a woman who initially seemed to have a common hair loss condition.

RNA-based treatments show promise for managing Hutchinson-Gilford Progeria Syndrome.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.