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Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

Some hair protein genes evolved early and were adapted for use in hair follicles.

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

New genetic mutations linked to rare skin disorders were found in three newborns.

Genes affect cytokine production, which can influence chronic diseases, and certain interventions may help prevent related molecular damage.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

DNA changes in tetraploid wheat improve root growth and nitrogen use.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

Men's and women's pattern hair loss progress differently, with men showing more hair thinning and women having more widespread hair loss.

Beta-sitosterol and stigmasterol might help prevent hair loss by blocking a specific enzyme.

Alopecia areata is an autoimmune disease where T cells attack hair follicles.

Eating a Mediterranean diet and taking certain supplements may improve symptoms of PCOS.

Some women with PCOS have rare genetic variants linked to the condition.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Scientists found a gene in mice that causes early hearing loss.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.