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Research from 2011 to 2020 shows androgen receptors could be key for prognosis and treatment in certain breast cancers.

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

The study concludes that regulating apoptosis could lead to new treatments for various skin and hair conditions.

High-dose finasteride may help treat glioblastoma but needs localized delivery for effectiveness.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Spermidine may improve skin health and hair growth by enhancing cell function.

Genetic predictions of baldness in Europeans don't apply well to African men.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

High CRP levels could indicate vitamin D deficiency in people with alopecia areata.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

The research found new potential mechanisms in mouse hair growth by studying RNA interactions.

STK11 gene variations do not predict how well metformin will work for PCOS, but may affect hair loss and excess hair growth.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

Cylindromas likely originate from hair follicle stem cells, not sweat glands.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Dermal fibroblasts have adjustable roles in wound healing, with specific cells promoting regeneration or scar formation.

Loose anagen hair syndrome may be caused by keratin gene mutations.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Significant progress was made in understanding PXE, but effective treatments are still needed.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Alcohol extract from Vernonia anthelmintica seeds may help treat stress-related hair loss.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

LEKTI is crucial for skin barrier and immune function, affecting conditions like Netherton syndrome and atopic dermatitis.

New hair regrowth therapies show promise but need more research.