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A gene mutation in mice causes permanent hair loss and skin issues.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

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.

The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

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.

Some blood-thinning medications can increase the risk of bleeding, and certain factors like genetics and other health conditions affect their safety and effectiveness.

Cutaneous Lymphadenoma is a unique skin tumor with specific protein markers and common gene mutations that may cause continuous cell growth.

Activating TLR9 helps heal wounds and regrow hair by using specific immune cells.

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.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

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

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

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

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.

The HIF-2α/ARNT complex is important for hair follicle development by controlling cell growth.

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.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.