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DHT affects bone growth by altering gene activity in osteoblasts, potentially complicating steroid use.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

Understanding gene expression in hair follicles can reveal insights into hair growth and disorders.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

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

Gene expression in hair follicles can help diagnose methamphetamine use disorder.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

EAAT4 decreases with age, harming skin function and calcium balance.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

ANp63 is crucial for skin integrity, new filaggrin gene mutations link to eczema, hair can regrow from non-stem cells, sunburns are increasing, and glucocorticoids help treat skin allergies by affecting immune cells.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

EDA2R gene linked to hair loss.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

RXRα is crucial for proper immune response and links diet to immune function.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

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

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

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

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

The gene URB is more active in human hair growth cells and responds to a hair-related hormone.

Turning off a specific gene in stem cells speeds up skin healing by helping cells move better.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.