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Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Human beard hair medulla contains a unique and complex mix of keratins not found in other human tissues.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

SHBG may be a useful early indicator and treatment target for PCOS.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

The hepatitis B vaccine did not cause hair loss in the tested mice.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

Women with AGA have higher lipid levels, increasing heart disease risk.

Different combinations of human hair keratins affect how hair fibers form.

Explosions don't stop hair proteins from being used to identify people.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Patients with advanced breast cancer and high hormone receptor levels who had surgery for ovarian/pelvic metastases lived longer, especially if they had high estrogen receptor levels.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

Dehydroepiandrosterone (DHEA) is a prohormone important for producing sex steroids and has potential health benefits.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

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

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

Mutant mice help researchers understand hair growth and related genetic factors.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

The p53 protein has complex, sometimes contradictory functions, including tumor suppression and promoting cell survival.

Keratins are important for skin cell health and their problems can cause diseases.

Finasteride can reduce fertility in some men, but stopping it increases sperm count.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Minoxidil affects collagen-related genes, potentially helping treat fibrosis.

Mobile phone radiation can cause DNA damage in human hair root cells.