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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

ILK is essential for skin development, pigmentation, and healing.

Natural gene therapy shows promise for treating skin disorders like epidermolysis bullosa.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

pH changes are crucial for root hair growth because they affect enzymes and proteins that control the cell wall and growth.

Sodium selenate was found to be safe and possibly slows Alzheimer's progression, but more research is needed.

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

Caffeine improves hair growth, thickness, and reduces shedding.

AGA treatments like minoxidil and LLLLT are safe and effective for gender minority patients.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

Mice with more Flightless I protein grew back their claws better after amputation.

Androgens can both increase body hair and cause scalp hair loss.

The paper suggests that hair loss might be caused by skull growth, not just DHT's effect on hair follicles, and calls for more research.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

A specific group of slow-growing stem cells marked by Thy1 is crucial for skin maintenance and healing in mice.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

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

Gene differences found in hair follicles linked to male baldness.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

CD61 is important for mouse tooth cell growth and works through Lgr5.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Two mouse mutations cause similar hair loss despite different skin changes.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

Epimedium extract helps increase skin pigmentation and could be a new treatment for conditions with reduced pigmentation.

Injecting CHIR-99021 into goose embryos improves feather growth by changing gene activity and energy processes.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.