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The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

The study found that specific proteins are markers of hair follicle development in human fetuses.

There is no significant link between alopecia areata and the PON1 enzyme polymorphisms studied.

The risk of skin tumors becoming malignant depends on the specific skin cell type affected.

Lanceolate complexes in mouse hair follicles are essential for touch and depend on specific cells for maintenance and regeneration.

Genes and hormones cause hair loss, with four genes contributing equally.

CT60 polymorphism might increase the risk of Alopecia Areata.

Some skin conditions are common during pregnancy and can be safely treated without affecting the pregnancy outcome.

Ectodysplasin signaling is crucial for skin appendage development, requiring specific doses and durations.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Skin problems are common in lupus, often appearing first, with various types and treatments, and careful monitoring is important for diagnosis and management.

Stem cells regenerate tissues and their behavior varies by environment, suggesting the hematopoietic system model may need revision.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

Asian hair is generally straight and thick, with unique disorders and properties, and more research is needed to understand it fully.

Hair loss risk is influenced by multiple genes.

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

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Natural gene therapy shows promise for treating skin disorders like epidermolysis bullosa.

Effective treatment for hidradenitis suppurativa varies, with antibiotics commonly used and surgery as an option, but no single method is universally successful.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

Eating less can improve stem cell function and increase lifespan.

Certain surgical methods are better than routine incision for hidradenitis suppurativa, topical clindamycin and acitretin are effective treatments, men with HS have a risk of skin cancer, HS patients are more likely to die from heart problems, and specific genetic markers are linked to treatment response.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.