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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A pathway helps maintain long telomeres in both stem and cancer cells.

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

Wnt signaling helps heal injuries and could lead to new treatments.

The Wave complex controls skin growth by suppressing certain signals.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Aire mutation reduces alopecia areata, while Notch4 mutation prevents it in mice.

Androgen signaling reduces Wnt activity, affecting prostate stem cell growth.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Matrical tumors share a common growth mechanism involving the Wnt pathway and consistent PHLDA1 expression.

Wnt/beta-catenin signaling in the skin helps fat cell development during hair growth and repair.

New genes linked to male pattern baldness were found on chromosome 20p11.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

H19 boosts hair growth potential by activating Wnt signaling, possibly helping treat hair loss.

Wnt ligand secretion by hair follicle cells is essential for hair growth and repair.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

A gene mutation causes monilethrix in a Chinese family.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Aging hair follicle stem cells can be rejuvenated by inhibiting Cdc42.

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