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An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Defects in certain proteins cause major heart abnormalities during early development.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A new gene mutation causes a rare type of hair loss.

Mcl-1 can activate Wnt signaling in skin cells, promoting growth and possibly cancer.

A boy with progeria had eye problems and signs of aging like hair loss and skin wrinkling.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

Myoblast transplantation shows promise for treating various muscle and heart conditions.

New hydrogel sensors can be quickly made and customized for wearable devices.

CD200- cells in hair follicles have a higher ability to regenerate hair.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

The hepatitis B vaccine did not cause hair loss in the tested mice.

Human hair follicles can be used to create heart muscle cells.

MARCKSL1 is important for wound healing and could be a target to reduce scarring.

Hex gene plays a crucial role in starting feather development in chick embryos.

Thymic LCH may be underdiagnosed, so thymic ultrasound should be considered in infants with cutaneous LCH.

RANKL improves the immune response against herpes simplex virus by enhancing T cell activation and could help develop better treatments or vaccines.

Dicer is crucial for hair growth in mice.

The patient with a misplaced pituitary gland and interrupted pituitary stalk is being treated with hormone replacement.

Deleting part of a gene in mice causes wavy hair and high pup loss.

The NF-κB effector p65/RelA activates hair keratin genes, aiding hair formation.

A boronic acid copolymer quickly forms cell clusters, useful for tissue and tumor modeling.

Diphencyprone initially increases mouse hair growth, then slows it, possibly due to changes in specific protein levels.

A new method allows detailed, continuous imaging of crustacean leg regeneration without harming the cells.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

Hair follicles supply a crucial brain development protein to the brain via platelets.

5-Bromo-3,4-dihydroxybenzaldehyde could potentially help hair growth by activating certain cell pathways and inhibiting others.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

Pediatric patients with dystrophic epidermolysis bullosa face more hospital admissions, procedures, and complications than others.