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Dihydrotestosterone treatment on 2D and 3D-cultured skin cells slows down hair growth by affecting certain genes and could be a potential target for hair loss treatment.

Malt1 protease is essential for regulatory T cell function and could be targeted to boost antitumor immunity.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

Exosomes from umbilical cord cells fix hearing loss and damaged ear hair cells in mice.

Stress hormone corticosterone blocks a growth factor to slow down hair stem cell activity and hair growth.

Alopecia areata is a hair loss condition caused by immune factors and can be treated with JAK inhibitors.

Aging skin shows thinner layers, fewer hair follicles, and new biomarkers like increased space between cells and smaller sebaceous glands.

Lymphatic vessels are essential for health and can be targeted to treat various diseases.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.

Cancer can hijack the body's cell repair system to promote tumor growth, and targeting this process may improve cancer treatments.

The research found that a complex gene network, controlled by microRNAs, is important for hair growth in cashmere goats.

Fat under the skin releases HGF which helps hair grow and gain color.

Male pattern hair loss may be linked to the developmental origins of hair follicles.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Thiazole, a sulfur and nitrogen chemical, is useful in creating potential drugs for conditions like seizures, cancer, bacterial infections, tuberculosis, inflammation, malaria, viruses, Alzheimer's, diabetes, and A1-receptor issues.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Melatonin may reduce skin damage caused by X-rays in rats.

Single Blimp1+ cells can create functional sebaceous gland organoids in the lab.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

Claudin expression changes help the skin respond to injury.

Poplar seed hairs grow from the placenta at the ovary base, with endoreduplication playing a key role in their development, and share similar cellulose synthesis processes with cotton fibers.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Light can activate hair growth through a pathway from the eyes to hair follicles.

Autophagy prevents early aging and maintains lipid and pheromone balance in mouse glands.