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Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

The circadian clock is crucial for tissue renewal and regeneration, affecting stem cell functions and having implications for health and disease.

Pregnancy can increase lupus activity, but careful planning and treatment can improve outcomes.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

The article concludes that better understanding gene regulation related to seasonal changes can offer insights into the mechanisms of seasonal timing in mammals.

A certain smell receptor in hair follicles can affect hair growth when activated by a synthetic sandalwood scent.

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

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

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Tiny needles with valproic acid can effectively regrow hair.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Stress increases certain chemicals in the skin and nerves, which might worsen skin conditions.

Mood stabilizers like lithium and anticonvulsants have side effects that can lead to patients stopping their medication, and managing these effects is important for treatment adherence.

Hair follicle stem cells are a promising source for tissue repair and treating skin or hair diseases.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Vitamin D receptor is crucial for starting hair growth after birth.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

FOXN1 gene variants cause low T cells and immune issues from birth.

K16 can partially replace K14 but causes hair loss and skin issues.

People often struggle to consistently use contraceptives and other medications, and long-acting options might be better for those who want to avoid daily doses.

Mothers and newborns with dental fillings had higher mercury in their hair, but getting fillings during pregnancy didn't raise mercury levels further.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

A mother's western diet can make her milk toxic, causing inflammation and hair loss in babies.

EGF and FGF help hair growth by affecting cell differentiation and fiber growth.

Scientists created early-stage hairs from mouse cells that grew into normal, pigmented hair when implanted into other mice.

Melanocyte precursors in human fetal skin follow a specific migration pattern and some remain in the skin's deeper layers.