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Activating cannabinoid receptor 1 reduces certain keratin levels, potentially aiding psoriasis treatment.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Prostate cancer cells can make their own androgens to activate the androgen receptor, and treatments like abiraterone may increase this ability, suggesting new therapies should target the entire steroid-making pathway.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

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

A genetic variant in goats is linked to cashmere growth.

Some women with PCOS have rare genetic variants linked to the condition.

Specific genes influence hair and cashmere growth in Laiwu black goats.

Four circRNAs were found to be significantly different in cashmere goat skin, affecting cashmere fineness.

VDAC2 promotes cell death in cashmere goat hair follicles through the P53 pathway.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

Researchers found genes that affect hair growth in Yangtze River Delta white goats.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Certain genes may help Bulgarians live longer.

Keratin 26 affects cashmere goat hair growth and is influenced by various treatments.

Differences in cashmere quality between goat breeds are linked to specific genes and pathways.

Cirsium japonicum flower extract increases melanin production and could help treat depigmentation conditions.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

miR-195-5p reduces hair growth ability in cells by blocking a specific growth signal.

c-Myc, Max, and Bin1 help hair follicle cells mature and die.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

Non-classical 21-hydroxylase deficiency can be missed in newborn screenings and should be considered in cases of early puberty or virilization.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.