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Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

A gene mutation causes woolly hair in a Syrian patient.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

Alopecia areata involves complex immune and genetic factors, with potential treatment targets identified, but more research is needed.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

The new method found new shared genetic areas linked to both Type 2 Diabetes and Prostate Cancer.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

Genes controlling hair growth and immune response are disrupted in male pattern baldness.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

New treatments for male hair loss show promise but need more research for safety and effectiveness.

Maritime pine bark has various chemical components useful for different industrial uses.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Men's sensitivity to male hormones might affect how severe COVID-19 gets for them.

Avoiding certain nutrients and drugs may help manage pemphigus.

Disrupting Smad4 in mouse skin causes early hair follicle stem cell activity that leads to their eventual depletion.