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Triparanol therapy can cause hair loss and skin dryness without inflammation or damage to hair follicles or skin structures.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Fish oil improves skin health in people with diabetes and high cholesterol.

Potassium levels affect blood sugar and insulin during dialysis, and malnutrition changes children's hair roots.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.

Nutrition can improve hair strength and reduce breakage.

Multiphoton microscopy is a promising tool for detailed skin imaging and could improve patient care if its challenges are addressed.

Signaling pathways are crucial for hair growth in goats.

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Focal alopecia in dogs has many causes and requires various tests for accurate diagnosis and treatment.

Chronic kidney disease can cause skin issues that need early recognition and combined treatment for better outcomes.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

A gene mutation in mice causes permanent hair loss and skin issues.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

A rat had a cyst similar to a hair follicle structure.

Rosacea is a skin condition with unclear causes, classified into four subtypes.

Alopecia areata involves immune response and gene changes affecting hair loss.

CD34+ cells from fat tissue help form hair follicles and blood vessels in skin.

Some recovered COVID-19 patients experience skin, hair, and nail issues, suggesting they need follow-up care.

Addressing biological changes in lipids, metabolism, and microbiota may help treat hair loss in young Chinese females with oily scalps.

VEGF helps squamous cell carcinoma grow in ways beyond just blood vessel formation.

Hormones significantly affect skin health, with vitamin D playing a key role.

New genetic factors linked to acne risk were discovered, highlighting the role of certain pathways and genes.

The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

Lupus can affect the scalp and nails, often causing hair loss and nail damage, and needs early aggressive treatment to prevent permanent damage.