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Longer anogenital distance may indicate a higher chance of having polycystic ovary syndrome, and measuring this distance along with hormone levels could improve diagnosis.

Regular follow-up visits, especially with dermatologists, can lower death rates for melanoma patients, with socioeconomic factors also affecting outcomes.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

DHT reduces a cell's ability to promote hair growth, while 3D culture without DHT improves it.

The endocannabinoid system affects oil production and inflammation in skin cells.

Zinc deficiency disrupts hair growth and cycle, but zinc supplements can fix this.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

The 2004 hair research meeting presented new findings on hair cell differentiation, genetic factors in hair loss, hair pigmentation, and potential targeted therapies.

Understanding phenotypic plasticity is crucial for developing effective cancer therapies.

Super-enhancers controlled by pioneer factors like SOX9 are crucial for stem cell adaptability and identity.

A protein from certain immune cells is key for new hair growth after skin injury in mice.

Different types of skin cells play specific roles in development, healing, and cancer.

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

High levels of male hormones, insulin resistance, and obesity are closely linked and worsen polycystic ovary syndrome, but more research is needed to improve treatments.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

The document concludes that a better understanding of cell changes during wound healing could improve treatments for chronic wounds and other conditions.

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

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

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

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Alopecia areata can cause unpredictable hair loss, and treatments like corticosteroids and minoxidil may help but have varying side effects.

Fat-derived stem cells, platelet-rich plasma, and biomaterials show promise for healing chronic skin wounds and improving soft tissue with few side effects.

The document concludes that there are no effective clinical treatments for hearing loss due to hair cell damage, but research is ongoing.

Inactive hair follicle stem cells help prevent skin cancer.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

The study found that immune responses disrupt hair growth cycles, causing hair loss in alopecia areata.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

FOXN1 gene variants cause low T cells and immune issues from birth.