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A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

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

TGF-β2 plays a key role in human hair growth and development.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

The Itpr3 gene causes a specific hair pattern in mice.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

CE-PTG is a better method for analyzing hair growth in androgenetic alopecia.

FTase and GGTase-I are essential for skin keratinocyte health.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

TSPO might help treat anxiety and depression.

Nitrate helps plants manage phosphate uptake and starvation responses through NIGT1 proteins.

Adding a small amount of TPGS to minoxidil can help hair growth, but too much TPGS reduces this effect and increases minoxidil in the blood.

Controlling transposable elements is crucial for successful tissue regeneration.

Prostaglandin D2 increases testosterone production in skin cells through a process involving reactive oxygen species, and antioxidants may help treat hair loss.

Activated ras can protect kidney cells from a certain substance that causes cell death.

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

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

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

Prostaglandin D2 increases testosterone production in skin cells through a process involving reactive oxygen species, which could be a new target for treating hair loss and other skin conditions driven by testosterone.

TRPS1 is crucial for bone, kidney, and hair follicle development.

Prostaglandin D2 increases testosterone levels in skin cells through reactive oxygen species, not enzymes, which could lead to new hair loss treatments.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.