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FERONIA regulates plant growth, pollen interactions, and sugar signaling.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

TPA promotes hair growth by increasing stem cell activity and activating specific cell signals.

A 23-year-old man has a benign, non-progressive hair loss patch that doesn't respond to treatment but can be cosmetically treated.

Nested PCR can reliably identify fungal infections when traditional methods fail.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Using testosterone-stimulated weanling rats can effectively replace castrated rats for anti-androgen testing, reducing animal stress.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

CCC1 is essential for pH balance and normal cell function in plants.

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

MYB30 and EIN3 work against each other to control root hair growth and phosphorus uptake in plants when phosphate is low.

Trichotillomania may have a genetic link to psychiatric disorders.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

Thermobalancing therapy is safe and effective for treating enlarged prostates.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

The IRE gene is important for normal root hair growth in Arabidopsis plants.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

Monoclonal antibodies LT-1, LT-2, and LT-7 help diagnose certain blood cancers.

Most cases of Temporal Triangular Alopecia are found in early childhood and may be related to genetic conditions.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

A specific gene mutation causes congenital hair loss.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

A unique gene mutation was found in a family with monilethrix.

IL-18 signaling helps mature Tregs move into the thymus.

A woman experienced fluctuating thyroid conditions and eye disease, but her symptoms improved with treatment.