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The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

SCD1 is crucial for skin health and overall energy balance.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Lack of Crif1 in hair follicle stem cells slows down hair growth in mice.

Foxp3+ Regulatory T Cells are important for immunity and tolerance, affect hair growth and wound healing, and their dysfunction can contribute to obesity-related diseases and other health issues.

Androgens increase muscle mass by promoting myoblast growth through ornithine decarboxylase.

Scientists restored fertility in male mice lacking a key fertility gene by using a modified gene.

Increasing ABC transporters in hair follicles may prevent chemotherapy-induced hair loss.

The meeting discussed medical findings, including benefits of certain treatments for cancer and heart conditions, and highlighted issues like poor adherence to preventive measures and skill gaps among interns.

Bexxar is highly effective as a first treatment for non-Hodgkin's lymphoma, with most patients alive and many in remission after eight years.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Aging in hair follicle stem cells leads to hair graying, thinning, and loss.

Lichen planopilaris is a rare, chronic condition causing hair loss, mainly in middle-aged women, and early treatment is important to prevent permanent baldness.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

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.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

The hair follicle infundibulum plays a key role in skin health and disease, and understanding it better could lead to new skin disease treatments.

The arrector pili muscle might play a role in hair loss and needs more research to understand its impact.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Hair follicle biology advancements may lead to better hair growth disorder treatments.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Endoglin is crucial for proper hair growth cycles and stem cell activation in mice.

Wnt signaling is important for development and cell regulation but can cause diseases like cancer when not working properly.

Stress may trigger hair loss by affecting immune protection in hair follicles.

Vitamin D3 analogs can promote hair growth in mice genetically prone to hair loss.

Finasteride inhibits enzyme activity in rhesus macaques, suggesting they're useful for evaluating similar drugs.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.