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Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

Hirsutism can be caused by various conditions besides PCOS, and it's important to treat the underlying issue and manage symptoms with medication and cosmetic approaches.

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

PDGF signaling is crucial for maintaining and renewing hair follicle stem cells, which could help treat hair loss.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

Macrophages help hair growth after injury through CX3CR1 and TGF-β1.

The study found that a specific area of the hair follicle helps start hair growth by reducing the blocking effects on certain cells and controlling growth signals.

CD98hc's role in skin health decreases with age.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Minoxidil improves blood flow and vessel flexibility, potentially helping with vascular stiffness.

Too much thymosin beta4 causes weird teeth and more hair growth in mice.

Mice can correct hair follicle orientation without certain genes, but proper overall alignment needs those genes.

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

Doctors should know how to diagnose and treat PCOS, which often involves checking for high male hormone levels and using medications to manage symptoms.

Alopecia areata is linked to thyroid autoimmunity but not type 1 diabetes.

Loss of keratin K2 causes skin problems and inflammation.

Dutasteride makes alcohol less sedating and may lead to less drinking in men.

Peginterferon alfa-2b and ribavirin therapy for hepatitis C can cause serious side effects, some different from those reported in clinical trials.

Early onset hair loss linked to genetics and androgen levels.

Smad1 and Smad5 are essential for hair follicle development and stem cell sleepiness.

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

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

Loss of Fz6 disrupts hair follicle and associated structures' orientation.

Genetic marker rs12558842 strongly linked to male hair loss.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

Autophagy is crucial for normal sebaceous gland function and sebum composition.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

Hair loss risk is influenced by multiple genes.

Dutasteride is more efficient than finasteride, but individual results vary.