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A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

New mouse models help study melanocytic cells for melanoma research.

ERG increases SOX9, promoting prostate cancer growth and invasion.

MPZL3 protein helps keep sebaceous gland size and cell growth in check.

BST2 is highly expressed in certain immune cells in alopecia areata, suggesting a role in the disease.

Chromosomal differences affect how muscle cells respond to testosterone.

FGF13 gene changes cause excessive hair growth in a rare condition.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

TBX3 gene affects pigmentation and marking formation in Dun Mongolian horses.

Blocking CXCR4 may help treat hidradenitis suppurativa.

Hoxc13 gene is essential for hair, nail, and papilla development.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

Mosaic Klinefelter syndrome can affect male fertility and may be missed in routine tests.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

BMI1 is essential for preventing hair greying and maintaining hair color.

Understanding genetics is crucial for treating heart and skin diseases.

A genetic hair protein variant is more common in Japanese people and is inherited.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

Females are more prone to lupus and arthritis due to X chromosome factors.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

Increasing Smurf2 hinders hair follicle stem cell differentiation and wound healing.

COX2 and ATP synthase control the size of hedgehog spines.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

Krox20 is important for maintaining stem cells in the skin and affects hair growth and color.

Removing SIX1 in fat cells reduces skin fibrosis.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.