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Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

The meeting discussed various skin conditions, treatments, and unusual cases, highlighting the effectiveness of tetracycline in treating rosacea.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

DSDs are birth conditions causing unusual sex development, managed with personalized care and sometimes surgery, but still lack a standard treatment approach.

Men may be more vulnerable to severe COVID-19 due to genetic and hormonal factors, but more research is needed.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

The research found that genetic factors for male pattern baldness in African men differ significantly from those in Europeans.

Conditions affecting sex development show that sexual diversity is a natural part of human variation.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Society's pressure to have children later in life favors genes that increase the risk of early baldness in male offspring.

AGA is caused by genetics and androgens, treatable with finasteride and minoxidil.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Hair follicle studies suggest that maintaining telomere length could help treat hair loss and graying, but it's uncertain if mouse results apply to humans.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Mutations in the AR gene cause hair thinning and loss.

Only a few hair-specific keratins are linked to inherited hair disorders.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

Understanding how EDC genes are regulated can help develop better drugs for skin diseases.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

A specific gene mutation causes congenital hair loss.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.