Search

everythinglearnresearchcommunity

for

Search:↓

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

A specific gene mutation causes long hair in Angora rabbits.

The scraggly mutation causes hair loss and skin defects in mice.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

Women with PCOS often have hirsutism and skin changes, which indicate a need for metabolic health checks.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Mutations in the KRT85 gene cause hair and nail problems.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The fuzzy gene is crucial for controlling hair growth cycles.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.

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

The Naked gene in mice causes abnormal sebaceous glands and disrupts hair follicle organization.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

Genetic testing is crucial before giving azathioprine to avoid severe side effects.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.