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The study found that diseases can be grouped by symptoms and that the accuracy of predicting disease-related genes varies with the data source.

Gene differences found in hair follicles linked to male baldness.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

Mutations in the WNT10A gene cause Short Anagen Hair syndrome and increase the risk of male pattern hair loss.

Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

Common baldness, also known as Androgenetic Alopecia, is caused by a combination of genetic factors and hormones called androgens.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

The article concludes that the wool follicle is a valuable model for studying tissue interactions and has potential for genetic improvements in wool production.

Alopecia areata is a genetic and immune-related hair loss condition that is often associated with other autoimmune diseases and does not typically cause permanent damage to hair follicles.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.

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

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Mutant mice help researchers understand hair growth and related genetic factors.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

FFA's causes may include environmental triggers and genetic factors.

New genetic discoveries may lead to better treatments for alopecia areata.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

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

Alopecia Areata has no guaranteed treatment for hair regrowth, but options like corticosteroids and minoxidil are used, with future research focusing on genetic and immune therapies.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Genetic defects in androgen production are linked to male developmental disorders and are improving treatment understanding.

Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.