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Laser therapy on human skin affects the HERC6 gene and related genes, influencing many cell processes and requiring careful safety measures.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

The hairless protein is important for skin, hair, and may influence cancer development.

A new mutation in the HR gene causes hair loss in a specific family.

A unique gene mutation was found in a family with monilethrix.

A girl had rickets due to a gene mutation affecting vitamin D response.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Hairless protein can block vitamin D activation in skin cells.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Mutations in the SNRPE gene cause hereditary hair loss.

Scientists discovered two versions of a new human hair keratin gene.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

Hes1 protein is important for hair growth and regeneration, and could be a potential treatment for hair loss.

TRH stimulates human hair growth and extends the hair growth phase.

Lack of KSR1 stops certain skin tumors in mice.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

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

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

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

New mutations in the hairless gene may cause hair loss and affect bone development.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The hHa7 gene is regulated by androgens in certain body hair, not scalp hair.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.