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The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Thioglycolic acid mainly affects the unordered areas in hair structure.

LC-MS/MS is more reliable than immunoassays for diagnosing 21-hydroxylase deficiency.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Blocking a specific enzyme can reduce the negative impact of stress hormones on hair growth cells.

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

Ornithine decarboxylase is crucial for human hair growth and the hair cycle.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

21-hydroxylase deficiency causes hormone imbalances leading to various symptoms, and diagnosis involves clinical and genetic tests.

p2y5, now called LPA6, is a receptor important for human hair growth.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Proper tissue repair in adult skin requires specific histone hypomethylation.

Cysteine strengthens hair, and glutamine fuels hair growth.

Lysophosphatidic acid boosts stem cell growth and movement by creating reactive oxygen species.

Enzyme purified and characterized for minoxidil sulphation in rat liver.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

Proteolytic activity in mouse skin changes with hair cycle stages, peaking in early anagen.

Women with hyperandrogenism have higher androgen levels and lower SHBG, which may contribute to conditions like excessive hair growth and early puberty.

Phospholipase A2 enzymes play key roles in skin health and disease.

Dermal EZH2 controls skin cell growth and differentiation in mice.

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

UTX is important for skin health and its loss can lead to skin issues, especially in females.