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Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

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.

Natural 5α-reduced glucocorticoids might be anti-inflammatory with fewer side effects than current options.

New research on prostamide F2α has led to treatments for glaucoma and eyelash growth and may have more medical uses.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

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

Steroids, particularly estrogens and 5α-reductase inhibitors, affect blood vessel-related hair growth processes in hair follicle cells.

The study found that mouse sweat glands develop before birth, mature after birth, and have specific keratin patterns.

Future osteoporosis treatments should focus on increasing bone growth, with many promising options available.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Finasteride effectively prevents biofilm formation and treats preformed biofilms, but requires high doses.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

The BMP2 gene is more active in the early growth phase of Cashmere goat hair and may affect hair regeneration and textile production.

An apple-based supplement was found to stimulate hair protein production, which may help with hair growth.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Hair growth is influenced by hormones and goes through different phases; androgens can both promote and inhibit hair growth depending on the body area.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Akt2 protein is essential for normal cell division in early mouse embryos.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Using special RNA to target a mutant gene fixed hair problems in mice.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.