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Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

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

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

Researchers found a way to create cells from stem cells that act like human cells important for hair growth and could be used for hair regeneration treatments.

Frontal fibrosing alopecia is linked to increased immune system activity and reduced stem cells, suggesting early treatment targeting this pathway might prevent hair follicle damage.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

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

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

Obese mice with a leptin gene mutation have a longer resting phase in their hair cycle, which may help understand certain hair loss conditions.

Ingenol mebutate gel changes gene expression related to skin development and immune response in actinic keratosis.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

ceRNA networks offer potential treatments for skin aging and wound healing.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

A girl with a rare skin condition improved after one month of treatment with acitretin.

The document concludes that hair loss and acne in women can be due to both androgen-related and unrelated causes, requiring a collaborative treatment approach.

Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

Effective PCOS treatments require targeting specific signaling pathways.

A child with a rare type of rickets showed some improvement with high doses of vitamin D, but such conditions often respond poorly to treatment.

The gene Endothelin 3 makes mice's fur darker by increasing pigment cells and pigment levels.

Deleting the CRIF1 gene in mice disrupts skin and hair formation, certain proteins affect hair growth, a new compound may improve skin and hair health, blood cell-derived stem cells can create skin-like structures, and hair follicle stem cells come from embryonic cells needing specific signals for development.

New factors in female hair loss include genetics, hormones, stress, and inflammation; future treatments should also focus on these areas and consider the patient's emotional well-being.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

Mice with human gene experienced hair loss when treated with DHT.