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Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Cancer can hijack the body's cell repair system to promote tumor growth, and targeting this process may improve cancer treatments.

Prostaglandin D2 blocks new hair growth after skin injury through the Gpr44 receptor.

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

The p53 protein has complex, sometimes contradictory functions, including tumor suppression and promoting cell survival.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

Hair can regrow after certain stem cells are lost because other stem cells can take over their role.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

Bimatoprost, a glaucoma medication, may also help treat hair loss.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

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

Prolactin may play a significant role in skin and hair health and could be a target for treating skin and hair disorders.

Estrogens generally inhibit hair growth and improve skin quality, but their exact effects on hair follicles are complex and not fully understood.

Men are more likely to get infectious skin diseases, while women are more prone to autoimmune and pigment-related skin conditions, influenced by biological and environmental factors.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Hair follicles in people with alopecia have lower levels of a key blood vessel growth protein.

Androgen receptor activity blocks Wnt/β-catenin signaling, affecting hair growth and skin cell balance.

Some natural compounds may help overcome drug resistance in certain cancers, but more research is needed.

Type 3 5α-reductase is more common and finasteride and dutasteride strongly inhibit it.

Eph/ephrin signaling is important for skin cell behavior and could be targeted to treat skin diseases.

Different species and human skin models vary in their skin enzyme activities, with pig skin and some models closely matching human skin, useful for safety assessments and understanding the skin's protective roles.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Fibroblasts, cells usually linked to tissue repair, also help regenerate various organs and their ability decreases with age. Turning adult fibroblasts back to a younger state could be a new treatment approach.