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

SHBG binding properties are unchanged in male liver cirrhosis patients.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

IL-1β inhibits human hair follicle growth.

PCAT1 helps hair growth by controlling miR-329/Wnt10b.

RNase L hinders hair growth by altering immune signals.

PRP preparation partially activates platelets, causing varied growth factor release.

Women with non-classical congenital adrenal hyperplasia have higher levels of certain steroids, which can be reduced by treatment.

Urotensin II increases growth and VEGF production in rat skin cells by turning on the Wnt-β-catenin pathway.

Biotin helps regulate proteins in the blood, which may explain its role in hair growth.

Super-enhancers control CD25 expression in specific cell types, affecting immune function.

Mutations in the hairless protein gene cause hair loss.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

GSK-36 downregulation with UTMD improves plaque stability in atherosclerosis treatment.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Allopregnanolone changes gene expression in glioblastoma cells.

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

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Certain genetic variations can make people more likely to experience hair loss and low white blood cell count from azathioprine.

BMP signaling affects hair color by interacting with the MC-1R pathway.

A specific gene change in APCDD1 increases the risk of hair loss.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

UC.145 may be a new biomarker for predicting gastric cancer.

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

A point mutation in the androgen receptor gene causes complete androgen insensitivity.