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The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

Alopecia areata is an autoimmune condition causing hair loss, influenced by genetics, stress, and diet, and may be prevented by a high soy oil diet.

Alopecia areata is a common autoimmune disease affecting about 2% of people, causing significant disability and often associated with mental health issues and other autoimmune conditions.

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

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Feed restriction in sheep leads to finer wool fibers but may reduce wool quality.

Early-onset baldness is linked to a higher risk of aggressive prostate cancer in African-American men, especially before age 60.

The research identified genes and pathways important for sheep wool growth and shedding.

Minoxidil, finasteride, and low-level laser light therapy are effective FDA-approved treatments for hair loss.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Stopping forehead irritation and using hydrocortisone helped a man's skin, Martinique has lower melanoma rates, a man had an allergy to a specific antifungal, another had unexplained cysts, certain drugs can cause skin reactions without always being interrelated, a link between Fanconi anemia and a skin condition was suggested, high levels of a certain protein may play a role in a type of psoriasis, and there's a need to study the connection between scalp pain and hair loss.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Seborrheic dermatitis is influenced by diet, genetics, and psychological factors.

Finasteride reduces prostate size and PSA levels in young patients.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Disulfide bonds in keratin fibers break more easily under stress, especially when wet, affecting fiber strength.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Hypothyroidism may cause certain types of hair loss.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Keratin 26 affects cashmere goat hair growth and is influenced by various treatments.