Search

everythinglearnresearchcommunity

for

Search:↓

Chemokine signaling is important for hair development.

Ice-skating athletes often have skin problems due to cold, infections, and inflammation, needing careful treatment and prevention.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Researchers identified new compounds in Platycladi Cacumen and found variations in its flavonoid content, which could aid in its quality control.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

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

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Androgen receptor activity blocks Wnt/β-catenin signaling, affecting hair growth and skin cell balance.

Human skin produces sex hormones like estrogen and testosterone, influenced by ARO and StAR, which may affect skin elasticity and hair growth.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

The enzyme 17β-HSD type 2 mainly performs oxidation in human sebaceous glands, which may help protect against acne.

New understanding of the causes of primary cicatricial alopecia has led to better diagnosis and potential new treatments.

Accurate diagnosis is key for treating different kinds of hair loss, and immune response variations may affect the condition and treatment results.

Prompt treatment of inflammatory tinea capitis (kerion) is crucial to prevent scarring and hair loss.

Lifestyle changes are the main treatment for PCOS, which is a complex condition requiring early management to reduce its health impacts.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Melanocyte precursors in human fetal skin follow a specific migration pattern and some remain in the skin's deeper layers.

Hair follicle regeneration possible, more research needed.

Women with polycystic ovary syndrome tend to have a longer distance between the clitoris and anus.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

Eph/ephrin signaling is important for skin cell behavior and could be targeted to treat skin diseases.

Hormones and neuroendocrine factors control hair growth and color, and more research could lead to new hair treatment options.

Understanding how melanocyte stem cells work could lead to new treatments for hair graying and skin pigmentation disorders.

Prolactin may be important for skin growth and immune function.

Different hair protein amounts change the strength of keratin/chitosan gels, useful for making predictable tissue engineering materials.

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

Neurosteroids change how GABA_A receptors work in the brain, which could be important for treating temporal lobe epilepsy.