Search

everythinglearnresearchcommunity

for

Search:↓

Sodium hypochlorite can effectively prevent and remove Staphylococcus aureus biofilms in atopic dermatitis at high enough concentrations.

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Specialized ribosomes affect aging in human skin cells.

Keratosis pilaris is a common skin condition causing a bumpy texture, sometimes linked to other diseases, with various treatments available.

Improving skin barrier and using antifungal treatments can help manage dandruff.

The 2006 editorial concluded that immunotherapy was advancing with new drugs, focusing on specific biological therapies and convenient oral treatments, and highlighted the importance of partnerships and new regulations in the field.

Tyrosine kinases are important in skin autoimmune diseases and could be targets for new treatments.

New targeted immunotherapies are improving treatment for inflammatory skin diseases.

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

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

The Hairless gene is crucial for healthy skin and hair growth.

The enzyme 25 Hydroxyvitamin D 1 α-Hydroxylase is essential for healthy skin and recovery after skin damage.

The meeting highlighted major advances in skin research, including new findings on skin microbes, genetic links to skin diseases, and improved treatments for various conditions.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Understanding skin structure and development helps diagnose and treat skin disorders.

Increased FGFR2b signaling, influenced by androgens, plays a role in causing acne.

Enzymes that change arginine to citrulline are important for skin barrier and hair formation, and their malfunction can lead to skin conditions and hair disorders.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

Gene network oscillations inside hair stem cells are key for hair growth regulation and could help treat hair loss.

ELL is crucial for gene transcription related to skin cell growth.

UV radiation may cause DNA changes in skin, certain UVB therapy helps psoriasis, a new gene mutation is linked to mild piebaldism, different immune cells affect psoriasis, a drug promotes hair growth, and some cancer drugs could treat skin barrier issues.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

The study found that tight junctions reach the top layer of the skin's stratum granulosum, not just the second top layer as previously thought.

Wnt ligands are crucial for hair growth and repair.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

The HR protein helps hair grow by blocking a hair growth inhibitor, aiding in hair follicle regeneration.

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