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The vitamin D receptor helps control hair growth and may protect against certain skin tumors.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

A genetic variant in the KRT25 gene causes tightly curled hair.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Low IRES/Cap translation is linked to higher stem cell potential.

Reducing FOXA2 in skin cells lowers their ability to grow hair.

Sfrp2 increases during hair follicle catagen phase and slows keratinocyte growth.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

Human hair protein patterns are inherited genetically.

Edar signaling is crucial for proper hair follicle development and function.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

High wool density in Rex rabbits is linked to specific gene activity affecting hair follicle development.

K6/ODC transgenic mice are effective for quickly identifying cancer-causing chemicals.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Women with excessive hair growth or polycystic ovary disease may more often carry a gene variant for 21 hydroxylase deficiency.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

The PP2A-B55α protein is essential for brain and skin development in embryos.

ASH2L is essential for skin and hair development.

A mutation in the KRTHB5 gene causes hair and nail issues.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Two siblings have a rare hair condition caused by a new genetic variant.

Researchers identified key genes and proteins linked to wool growth in sheep.

Understanding the APCDD1 gene can lead to new hair loss treatments.

Urtica dioica extract may help treat androgenic skin diseases by reducing a specific gene's activity.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.