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New methods have greatly improved our understanding of stem cell behavior and roles in the body.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Prolactin affects when mice shed and grow hair.

The document concludes that targeting the androgen receptor may be a promising breast cancer treatment, especially for certain types.

Skin bacteria, specifically Staphylococcus aureus, help in wound healing and hair growth by using IL-1β signaling. Using antibiotics on skin wounds can slow down this natural healing process.

Human hair's ability to get wet is complex and can change with treatments, damage, and environment.

Certain microRNAs in the fluid around eggs are linked to Polycystic Ovary Syndrome and may help diagnose it.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

To diagnose Polycystic Ovarian Syndrome, two out of three signs—irregular periods, high male hormone levels, or cysts on the ovaries—are needed.

People with atopic dermatitis are more likely to develop other skin conditions due to shared genetics and immune pathways.

Blocking a specific protein signal can make hair grow on mouse nipples.

Finasteride reduces PSA levels, terazosin doesn't affect them, and tracking prostate cancer in patients taking finasteride could be difficult.

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

Hair proteins have weak spots in their α-helical segments.

Lichen planopilaris mostly affects women with fair skin and can look different on each person, needing early treatment to prevent hair loss.

New sulfur-containing steroid analogs show promise for more targeted medical treatments.

The skin's basement membrane has specialized structures and molecules for different tissue interactions, important for hair growth and attachment.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

People with lichen planus are more likely to have dyslipidemia, especially higher triglyceride levels.

Sensitive skin often causes discomfort, affects many people, especially women and older adults, and should be managed with careful product selection.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Catalytic antibodies are early indicators and active participants in the development of systemic lupus erythematosus.

Skin stem cells are maintained by signals from nearby cells and vary in their ability to renew and mature.

Platelet-rich plasma is most effective for hair loss treatment and wound healing in skin surgery, but more research is needed for consistent results.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

ARL15 is important for fat cell development and the release of the hormone adiponectin.