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Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

New treatments targeting specific genes show promise for treating keratin disorders.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Rice bran extract caused moderate skin irritation but no eye irritation, while a diluted essence was not irritating to skin and only slightly to guinea pigs.

Targeting cholesterol, fatty acids, fibrosis, and mast cells may help treat CCCA.

The hepatitis B vaccine did not cause hair loss in the tested mice.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Hair follicle regeneration is possible but challenging, especially in humans, due to the need for specific cells and a better understanding of how they signal growth.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Bright light during the day doesn't change most human clock genes but may slightly increase Rev-erb-ß.

Scientists have developed a new method to detect steroid abuse in athletes using cell-based tests, which could be the future of anti-doping methods.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

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

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

Understanding gene expression in hair follicles can reveal insights into hair growth and disorders.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Human hair follicle stem cells can be isolated using specific markers for potential therapeutic use.

A gene variation is linked to hair thickness in Asians.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Finasteride exposure affects gene expression and anogenital distance in male rat fetuses.

Nanotechnology is improving drug delivery and targeting, with promising applications in cancer treatment, gene therapy, and cosmetics, but challenges remain in ensuring precise delivery and safety.

Hair restoration techniques have improved but still rely on limited donor hair, with new methods like cloning and gene therapy being explored.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.