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The genetic variant studied does not affect PCOS symptoms in Kashmiri women.

EGFR is essential for normal hair development and follicle differentiation.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Gut bacteria may affect hair loss risk.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Macrophages help heal nerves by aiding the maturation of Schwann cells and are important for nerve repair.

Black women with CCCA are more likely to have uterine fibroids.

Tiny particles from 3D-grown skin cells speed up wound healing by promoting blood vessel growth.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

Hypothyroidism may cause certain types of hair loss.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Scientists turned mouse stem cells into skin cells that can grow into skin layers and structures.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

PTHrP and its receptor can control blood vessel growth and hair development in mouse skin.

Macrophage iron release is crucial for hair growth and wound healing.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

Hair follicles supply a crucial brain development protein to the brain via platelets.

Genetic discoveries are leading to new treatments for alopecia areata.

Blocking certain immune signals can reduce skin damage from radiation therapy.

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

FGF5 gene mutations cause long hair in domestic cats.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

Fat tissue and a specific protein are crucial for healthy hair growth and maintenance.

Anorexia Nervosa and Bulimia Nervosa are complex eating disorders with increasing incidence among young females, significant morbidity, and varying mortality rates, requiring more research for better treatment.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.