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A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

Older parental age, rural living, and specific genetic mutations increase hypospadias risk in children.

PBM helps improve cell survival in 3D tissue engineering.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

CD73 may regulate hair growth and could be targeted for hair growth treatments.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

The hr gene is linked to hair loss in Valle del Belice sheep.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

PNU 157706 is a more effective treatment than finasteride for conditions caused by DHT, like enlarged prostate and hair loss.

Dlx3 is essential for hair growth and regeneration.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

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

Exosomal miR-199a-3p from dermal papilla cells helps control hair color by affecting melanocytes.

TPA strongly increases ODC activity in certain skin cells, potentially aiding tumor growth.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

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

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

High TSPEAR levels in colorectal cancer predict worse outcomes.

FGF signaling is crucial for starting feather development in chicken embryos.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

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

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

S100A3 protein is crucial for hair shaft formation in mice.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

miR-200c-3p could help diagnose and treat alopecia areata.

ALKBH5 helps wounds heal faster by stabilizing PELI2 mRNA.