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Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Rice bran oil extracted by supercritical CO2 is considered non-genotoxic.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

Notch signaling disruptions can cause various skin diseases.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Different forms of FGF5 either promote or inhibit hair growth.

Human skin can make serotonin and melatonin, which help protect and maintain it.

Spironolactone might lower the chance of getting rosacea.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

The document concludes that the girl's hairlessness is likely inherited from her parents.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

CRH in the skin acts like the body's stress response system, affecting cell behavior and immune activity.

Finasteride for hair loss may cause persistent sexual symptoms, depression, anxiety, and lower quality of life.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Melatonin is important for skin health and protection, and can be made by the skin or applied to it.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Mouse skin can produce and process serotonin, with variations depending on hair cycle, body location, and mouse strain.

PRP treatment can safely improve short-term vision in acute NAION patients.