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Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Different scalp and hair disorders are more common in certain ethnic groups, with the most common being androgenetic alopecia, which is treated with medications like minoxidil and finasteride.

Hair loss in men treated best with early medication or transplant, new treatments researched.

Androgen receptors are active in many tissues of both male and female mice, not just reproductive organs.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

New genetic locations explain much of hair color variation in Europeans.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Understanding wool keratin-associated proteins in sheep can help improve wool quality through selective breeding.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

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

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Sheep and goat hair fibers are complex due to keratin-associated proteins, which are important for fiber properties and growth.

Inflammation may be linked to hair loss, and targeting specific enzymes could help treat it.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Two mouse mutations cause similar hair loss despite different skin changes.

Androgens contribute to common male hair loss; more research needed for hair growth medication.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Understanding hair growth involves complex factors, and more research is needed to improve treatments for hair loss conditions.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

Genetic marker rs12558842 strongly linked to male hair loss.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Terbinafine can cause hair loss.

Cyclosporin doesn't stop hair loss.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

Hair loss gene found on chromosome 3q26.

Hormones and genes affect hair growth and male baldness.