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Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

Changes to the Foxp3 protein affect how well regulatory T cells can control the immune system, which could help treat immune diseases and cancer.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

Finasteride and minoxidil are effective FDA-approved treatments for androgenetic alopecia.

Many treatments for hair loss lack proper testing and FDA approval, so their effectiveness is uncertain.

Treat pattern hair loss with finasteride and topical minoxidil.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Lower zinc levels may predict less effective hair loss treatment.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

S100A4 and S100A6 proteins may activate stem cells for hair follicle regeneration and could be potential targets for hair loss treatments.

FLRG and follistatin have different roles in wound healing.

LEF1 interacts with Vitamin D Receptor, affecting hair follicle regeneration and this could be linked to hair loss conditions.

Pantothenic acid helps mink hair follicles grow by affecting certain cell signals.

Male rats have androgen receptors in their liver, which are different from proteins that bind estrogen.

Retinoic acid-binding proteins in skin are regulated by β-catenin and Notch signalling.

Estrogen affects how vitamin A is processed in mouse skin, which may impact acne treatment, hair growth, and skin defense.

C60 fullerenes can alter protein function and may help develop new disease inhibitors.

A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.

Charnoly bodies could be a marker for cell damage, and certain nutrients and proteins might prevent them, potentially helping with brain diseases and cancer.

New androgen receptor modulators show promise for treating diseases like prostate cancer and muscle wasting.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

The research provides insights into hair follicle growth in forest musk deer by identifying key genes and pathways involved.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Modified stem cells from umbilical cord blood can make hair grow faster.

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

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

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.