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PCOS is a common condition in women that causes various symptoms and health issues, treatable with lifestyle changes and medication.

Progeria, a disease that causes early aging, is linked to a gene mutation and helps us understand normal aging.

Genetically repaired stem cells may treat certain genetic diseases, Th17 cells are key in fighting systemic fungal infections, hair loss in AGA is due to progenitor cell loss, and α-synuclein transfer might contribute to Parkinson's disease progression.

Planarian regeneration begins with a specific gene activation caused by injury, essential for healing and tissue regrowth.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Short-chain fatty acids from *Cutibacterium acnes* cause skin inflammation, contributing to acne.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

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

The conclusion is that small hair follicles cause baldness in macaques, and treatments like antiandrogens and minoxidil can prevent hair loss and promote regrowth.

Low and ultralow doses of flutamide can cause liver damage in young women with high androgen levels, regardless of dose or birth control use, with higher risk for those with higher BMI and liver enzyme levels before treatment.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

Volatile organic compounds can cause inflammation and increase the risk of autoimmune diseases.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

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

Androgens can both increase body hair and cause scalp hair loss.

Acne is a chronic skin condition not caused by poor hygiene or diet, and it requires long-term treatment and patient education.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Different hair and scalp disorders cause hair loss or excess hair growth, with various treatments available depending on the specific condition.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

Frontal fibrosing alopecia is a challenging hair loss condition with no known cause or definitive treatment.

Current treatments for common male hair loss have limited effectiveness and can cause side effects.

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

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.