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Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

The document explains the genetic causes and characteristics of inherited hair disorders.

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

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

PCOS has a strong genetic basis, but more research is needed to fully understand it.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

Anorexia Nervosa and Bulimia Nervosa are complex eating disorders with increasing incidence among young females, significant morbidity, and varying mortality rates, requiring more research for better treatment.

The visfatin GT genotype may increase the risk of Alopecia Areata.

Recent selection on immune response genes was identified across seven ethnicities.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

Selective breeding can enhance immunity in dairy cattle.

Human hair keratins can self-assemble and support cell growth, useful for biomedical applications.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Gene mutations can cause problems in male genital development.

A woman was allergic to quinine in her anti-hair loss lotion.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

PCOS may have evolved as an advantage in past environments with food scarcity.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.