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Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

Wild strawberry waste extract can be a sustainable cosmetic ingredient for treating acne and hair loss.

Certain gene variations are linked to the thickness of cashmere goat hair.

ERG increases SOX9, promoting prostate cancer growth and invasion.

CRH in the skin acts like the body's stress response system, affecting cell behavior and immune activity.

Overexpressing a specific enzyme in mice causes hair loss and female infertility.

GLP-1 receptor agonists, like Dulaglutide, Liraglutide, and Semaglutide, have potential benefits beyond the pancreas, including neuroprotection, pain suppression, cardiovascular protection, obesity management, and cancer treatment, but there are concerns about pancreatitis and pancreatic cancer risks.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

Androgens increase muscle mass by promoting myoblast growth through ornithine decarboxylase.

Alternating treatment with two drugs could help cells in a rapid aging disease.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

KCNQ potassium channels help control the sensitivity of touch receptors in the skin.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

A specific mutation in PA-PLA1α causes abnormal hair growth.

SOX9 is essential for the development of various organs and hair follicles.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

Inherited color dilution in rabbits is linked to DNA methylation changes.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

A new therapy for a skin blistering condition has not been developed yet.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.