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Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

Melatonin improved mental health and metabolism in women with PCOS.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

Spironolactone may make some cancer treatments more effective by blocking a protein that helps cancer cells survive.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Some men's prostate tissues have low enzyme levels due to genetic changes, possibly affecting treatment for prostate enlargement.

The 2004 hair research meeting presented new findings on hair cell differentiation, genetic factors in hair loss, hair pigmentation, and potential targeted therapies.

Genetic variations affecting skin structure play a key role in severe acne.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

The study found that giant pandas have more melanin in black hair follicles than white, with gene expression differences that could affect hair color and skin health.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Balding scalps show different gene expressions affecting hair growth compared to non-balding scalps.

Researchers found 15 new genetic links to skin traits in Japanese women.

Researchers found two new genetic variants linked to Alzheimer's disease.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

Ingenol mebutate gel changes gene expression related to skin development and immune response in actinic keratosis.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

A specific genetic deletion in goats affects cashmere yield and thickness.