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Tetrathiomolybdate reduces hair growth marker in skin cells by boosting harmful oxygen molecules, but effects can be reversed.

Specific mutations in a receptor cause facial abnormalities and hair loss.

A gene mutation in mice causes skin defects and early death.

Cathepsin E is crucial for normal skin cell differentiation and development.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

Cell-based therapy using specific immune cells may help treat alopecia areata by promoting hair regrowth.

Avian yolk antibodies offer a promising, ethical alternative for disease prevention and therapy.

A 25-year-old man with multiple skin tumors was successfully treated with acitretin and methotrexate.

Uterine transplants for transgender women are feasible but need more research.

Taurine is important for many body functions and its deficiency can cause health problems.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

New mutations in the hairless gene may cause hair loss and affect bone development.

The E2 protein affects gene activity in hair follicles of mice.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Rapamycin and anti-EGFR antibody reduce LAM/TSC cell migration and blood vessel growth in the uterus.

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

α-Ketoglutaric acid improves hair growth, rabbit performance, and antioxidant levels.

A specific metabolite, not a receptor protein, triggers the production of certain kidney enzymes, but this process is disrupted in mice with a mutation causing testicular feminization.

Urtica dioica extract may help treat androgenic skin diseases by reducing a specific gene's activity.

Dutasteride potentially improves cell survival and reduces retinal damage in retinitis pigmentosa.

Different androgen concentrations affect wool-related gene expression differently in Hetian and Karakul sheep breeds.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requires high doses of calcium and vitamin D for management.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

α-MSH increases melanin production in moulting hair follicles, while AVT inhibits it.

Modified β-catenin can cause different effects in mouse skin cells, leading to cysts or tumors depending on the cell type.

A mutant FERONIA gene affects root hair growth at high temperatures.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.