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ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The KAP 7 gene affects wool traits in Rambouillet sheep, with the BB genotype showing the best wool characteristics.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

The study found nine new hair protein genes in human hair follicles.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

New mutations in the hairless gene may cause hair loss and affect bone development.

Overexpression of COX-2 causes early hair loss in mice, but can be prevented with a COX-2 inhibitor.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

ATP increases melanin production in skin after UV exposure, with the P2X7 receptor being crucial for this process.

Krox20 (Egr2) is important for the function of epithelial stem cells.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

Phospholipids help plant proteins move by regulating receptor interactions.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

The protein CCN2 controls hair growth by affecting hair follicle formation and stem cell activity in mice.

Three genes, BMP4, POSTN, and WNT5A, may help treat keloids.