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Hair follicle stem cells are crucial for touch sensation and proper nerve structure in mice.

The Kras mutation changes normal cell signals, leading to disrupted tissue structure and potential cancer.

Topical minoxidil is the best-supported treatment for female hair loss, but personalized plans are needed.

Human hair is made up of different keratins, some strong and some weak, with specific types appearing at various stages of hair growth.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Nanoparticles can deliver vaccines through hair follicles, triggering immune responses and providing protection.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Three genes in Arabidopsis are important for plant growth and development by affecting sugar attachment to proteins.

Spermidine may help reduce hair loss and deserves further testing as a treatment.

Cyclic nucleotide-gated channels are crucial for proper root hair growth and calcium balance in plants.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Cat claws stay sharp by shedding their outer layer through microcracks formed during activities.

Insulin resistance might not be enough to worsen blood vessel function in young, nonobese women with polycystic ovary syndrome.

Blocking the Wnt/β‐catenin pathway can speed up wound healing, reduce scarring, and improve cartilage repair.

Certain RNA molecules are important for the development of wool follicles in sheep.

Zebrafish helped find new ways to prevent drug-induced hair cell death and potential treatments for hearing loss.

Reducing Tyrosinase prevents mature color pigment cells from forming in mouse hair.

Androgenetic alopecia significantly harms quality of life, affecting emotions and relationships.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Higher testosterone levels can increase the risk of certain diseases like type 2 diabetes in women and prostate cancer in men, but can also protect against autoimmune diseases and hair loss. It also affects body fat and bone density.

Hormones affect prostate health and disease, with certain hormone imbalances linked to prostate cancer and benign prostatic hyperplasia.

People with Alopecia areata often have lower Vitamin D levels, which might affect the severity of their condition.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Older men with low levels of a testosterone byproduct had a higher chance of developing an irregular heartbeat.

KCNQ potassium channels help control the sensitivity of touch receptors in the skin.

Cattle skin has leptin which might control skin and hair growth.

Child abuse is linked to higher BMI, but not because of hair cortisol or cortisone levels.