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The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

SOX9 is crucial for cell development and repair but can cause fibrosis and cancer if misregulated.

Certain genes control the color of human hair by affecting pigment production.

TGF-β and TNF influence hair follicle cell fate, with TNF being more effective in triggering cell death.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

SOX11 and SOX4 help skin cells act like embryonic cells to heal wounds in mice.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

EGM2 and SOX2 help form beige adipocytes by maintaining ASC immaturity and activating brown adipocytes.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

Most patients with Tuberous sclerosis had neurological or skin issues, and over half had psychiatric problems.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Keratin 75 is important for fast wound healing and works with SOX2 and the LINC complex to help skin cells move and repair damage.

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

Targeting the TRPV4 channel may help treat intestinal diseases.

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

miR‑339‑5p can slow down hair follicle stem cell differentiation by targeting DLX5.

As skin cells mature, vitamin D receptor levels decrease while retinoid X receptor α levels increase.

Dermal EZH2 controls skin cell growth and differentiation in mice.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

ETS2 drives cancer progression in squamous cell carcinoma and is linked to poor patient outcomes.

The Bethesda system is effective for identifying thyroid cancer but has low sensitivity.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Clinicians should be aware of alternating thyroid conditions and their treatment.

The authors clarified data overlap and corrected a figure error, apologizing for any confusion.

Sox9 is present in most canine skin tumors and may help understand stem cells' role in these cancers.

Testosterone treatment may affect heart response to stress in transgender men.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

Trichostatin A helps restore hair-growing ability in skin cells used for hair regeneration.