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The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Docetaxel and paclitaxel for breast cancer can cause permanent, severe hair loss.

A gene variation is linked to hair thickness in Asians.

Half of the patients treated with a specific drug for skin cancer experienced hair loss not related to the drug's dosage.

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

Researchers found a genetic region that influences the number of coat layers in dogs.

A gene mutation causes woolly hair in a Syrian patient.

The document concludes that DAB389-IL2 is promising for treating refractory cutaneous T-cell lymphoma, but more research is needed on its effectiveness and side effect management.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

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

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Netherton Syndrome can cause severe skin lesions in rare cases.

A new gene mutation causes insulin resistance in a girl and her mother.

A new gene variant causes glucocorticoid resistance in a mother and son.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Different types of long-lasting stem cells are responsible for the growth and upkeep of the mammary gland.

Melatonin affects many body functions beyond sleep by interacting with specific receptors in various tissues.

Understanding gene expression in hair follicles can reveal insights into hair growth and disorders.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

Human skin can make serotonin and melatonin, which help protect and maintain it.

Super-enhancers controlled by pioneer factors like SOX9 are crucial for stem cell adaptability and identity.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.