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

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

KRTAP2 genes are crucial for hair structure and may impact hair disorders and treatments.

H3K4me3 helps control RSPO3 to influence hair growth and development.

Lack of FPR2 slows hair growth by affecting hair cell activity.

The research suggests that SFRP2 and PTGDS proteins might be indicators of female pattern hair loss and could contribute to hair loss.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

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

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Spermidine may improve skin health and hair growth by enhancing cell function.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

Inhibiting SFRP1 may help treat hair loss.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Higher SRD5A2 expression predicts better response to finasteride in treating urinary symptoms.

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

PrPC is important for neural differentiation in cattle and mouse embryonic stem cells.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

A new gene variant causes curly coats in some dog breeds.

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

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

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

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Two specific genes are more active during hair growth in mice.

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

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.