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Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

A child with a rare type of rickets showed some improvement with high doses of vitamin D, but such conditions often respond poorly to treatment.

HLD10 can include increased body hair and Mongolian spots.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

Longer CAG repeats in gene linked to more severe hair loss in females.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

A certain gene variation can affect protein production and is linked to male pattern baldness.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

A rare genetic mutation in the EGFR gene caused severe skin issues and other health problems in a Slovakian girl, who is now 4 years old and receiving care.

Certain IL-18 gene variations may increase the risk of alopecia areata.

The Cyp11a1 gene variation has a weak link to PCOS, but higher di-hydro-testosterone levels are found in PCOS patients.

A mutation in the KRT25 gene causes woolly hair and hair loss.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

The CTLA-4 gene polymorphism does not affect polycystic ovarian syndrome.

Keratin heterodimers are preferred for their specific and structural advantages.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

Certain gene variations are significantly linked to hair loss, especially in white people.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

A new mutation in mice causes crooked whiskers and messy hair.

Different forms of finasteride dissolve and remain stable differently, affecting capsule quality.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Genetically modified rats help reveal how vitamin D affects bone and skin health.