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A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Targeting the p300/AR axis may help treat polycystic ovary syndrome.

Early diagnosis of PSIS can lead to normal height with growth hormone and testosterone treatment.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Activating STAT5 in the skin's dermal papilla is key for starting hair growth, regenerating hair follicles, and healing wounds.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

Ptprq has multiple forms that change during inner ear development.

In STSD patients, the body compensates for low androgen levels by increasing another enzyme's activity.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

MPA increases cancer spread by boosting Eph A2 activity.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

Akt2 protein is essential for normal cell division in early mouse embryos.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

Compounds from Pterocarpus indicus may help treat benign prostatic hyperplasia by stopping cell growth.

TSPO might help treat anxiety and depression.

PTHrP is important for bone formation and may be targeted for osteoporosis treatment and longevity therapies.

Lower SMAD2/3 activation predicts more severe skin cancer.

The PP2A-B55α protein is essential for brain and skin development in embryos.

Somatostatin may help protect hair follicles from immune attacks.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.