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

Hormones, especially androgens, play a big role in acne, but most acne sufferers don't have a hormone disorder. Hormonal treatments, including birth control pills, can be very effective for women whose acne doesn't improve with regular treatments.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Trilostane effectively and safely treats dogs with pituitary-dependent hyperadrenocorticism, improving symptoms and adrenal gland size.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Animals that change color with the seasons mainly do so in response to daylight changes, but climate change is causing camouflage problems that may require evolutionary changes.

Blocking the Wnt pathway could lead to new treatments for cancer and tissue repair but requires careful development to avoid side effects.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Hair color production is closely linked to the active growth phase of hair in mice and may also influence hair growth itself.

Lowering testosterone speeds up wound healing in male mice.

Researchers found that hair shedding happens mostly when new hair is growing and involves a unique process.

Skin-derived precursors in hair follicles come from different origins but function similarly.

C60 fullerenes can alter protein function and may help develop new disease inhibitors.

FGF signaling is a promising target for developing treatments for wounds, metabolic diseases, and cancer.

Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

Hair loss in men treated best with early medication or transplant, new treatments researched.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

The document concludes that adult mammalian skin contains multiple stem cell populations with specific markers, important for understanding skin regeneration and related conditions.

Sensitive skin is often caused by nerve fibers and environmental factors, and can be managed with mild skincare and professional advice.

Melanocytes are crucial for skin pigmentation and can affect conditions like melanoma, vitiligo, and albinism, as well as hair color and hearing.

Fatty acid transport protein 4 is essential for skin and hair development.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

The circadian clock is crucial for tissue renewal and regeneration, affecting stem cell functions and having implications for health and disease.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.