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A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

High TSPEAR levels in colorectal cancer predict worse outcomes.

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

lncRNAs may regulate hair follicle development in Hu sheep.

Specific mutations in a receptor cause facial abnormalities and hair loss.

Key genes linked to hair growth and cancer were identified in hairless mice.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

A newly found RNA in Cashmere goats may play a role in hair growth and development.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Exosomes from stem cells can reduce UV-induced skin damage by lowering inflammation and oxidative stress.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

IL-26 has antimicrobial and pro-inflammatory effects in the chronic skin condition Hidradenitis Suppurativa.

Some women with excess hair growth have a hormone condition that can't be diagnosed by blood or urine tests alone.

IGF2BP3 gene is up-regulated in keloid patients, suggesting potential targets for treatment.

AR-27 E-Chol siRNA can effectively promote hair regrowth for androgenetic alopecia.

MCHR2 gene duplications may be linked to alopecia areata.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Gasdermin A3 overexpression in skin causes inflammation and hair loss.

ULBP3 could be a marker for diagnosing alopecia areata incognita and may be linked to its cause and development.

ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.

Alpha-MSH affects mitochondrial function, and MC1R mutations may increase skin aging.

A mouse gene mutation increases the risk of skin cancer.

MicroRNA-148a is crucial for maintaining healthy skin and hair growth by affecting stem cell functions.

Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.