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Prolactin contributes to hair loss by promoting hair follicle shrinkage and cell death.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

HDAC inhibitors help brain cells grow and improve brain function.

Sgk3 kinase is essential for normal hair growth in mice.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

The SLICK1 allele in Holstein heifers affects hair and immune traits without altering prolactin signaling.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

QLT0267 stops hair follicle cell growth and movement.

GDNF signaling helps in hair growth and skin healing after a wound.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Targeting the HEDGEHOG-GLI1 pathway could help treat keloids.

Ginsenoside Rb1 slows down aging in mice by affecting cell growth, cell death, and metabolism.

HLD10 can include increased body hair and Mongolian spots.

A woman with chronic hepatitis C had a rare skin condition linked to her illness.

CHI3L1 and CXCL5 proteins help promote hair growth.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Drugs that block GSK-3 show promise for treating various diseases.

A gene mutation in Lama3 is linked to a common type of hair loss.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

PTHrP and its receptor can control blood vessel growth and hair development in mouse skin.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Nelfb is essential for dermal fat development and survival.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.