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Small proline-rich proteins and trichohyalin help make epithelial tissues tougher and more flexible.

Actinic keratosis can lead to skin cancer, is more common in fair-skinned people, and can be reduced with sunscreen and treated effectively.

Vemurafenib causes skin side effects similar to RASopathies, requiring regular skin checks and UVA protection.

Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

Activin A helps heal skin wounds and protects the brain after injury.

Fatp4 is crucial for healthy skin development and function.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Erosive pustular dermatosis is a rare skin disease that's hard to treat and affects the scalp or legs.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

The conclusion is that understanding how hair follicle stem cells live or die is important for maintaining healthy tissue and repairing injuries, and could help treat hair loss, but there are still challenges to overcome.

In vivo reflectance confocal microscopy is useful for evaluating hair shaft diseases but needs improvement for deeper hair follicle issues.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

The guidelines help doctors manage skin problems from certain cancer treatments to improve patients' lives.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

The new patch for treating mouth sores releases medicine slowly, sticks well, and helps healing without the side effects of current creams.

Early treatment of EPDS can improve outcomes and reduce recurrence risk.

Dermoscopy improves diagnosis of hair and scalp disorders and can help avoid unnecessary biopsies.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

The document concludes that using a person's own fat cells (SVF) can significantly increase hair thickness and density, suggesting it could be a promising treatment for hair loss.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Some young Angus cattle had skin problems due to not enough vitamin A, which got better after they were given more vitamin A.

New genetic mutations linked to rare skin disorders were found in three newborns.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Regenerative cellular therapies show promise for treating non-scarring hair loss but need more research.