Search

everythinglearnresearchcommunity

for

Search:↓

Researchers found that hair follicle stem cells can become squamous cell carcinoma due to Ras activation, which could lead to new treatments.

Dark skin has stronger barriers and structure due to specific gene activity.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

Mitochondrial genes help predict breast cancer outcomes and spread.

YAP and TAZ are crucial for skin cell growth and repair.

The condition might be caused by genetic changes after birth.

The ACE1 gene variant doesn't affect long-COVID symptoms.

A new molecule was found to be a safe and effective skin lightener and anti-aging product.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

A specific gene change in APCDD1 increases the risk of hair loss.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

Certain miRNAs may play a role in sheep hair follicle development, which could help improve wool production.

Low oxygen levels affect the behavior of certain proteins in human skin cells.

Activated LEF/TCF complexes are crucial for hair development and cycling.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Higher SRD5A2 expression predicts better response to finasteride in treating urinary symptoms.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

KLHL24-mutant stem cells help understand skin and heart disease.

Fatty acid transport protein 4 is essential for skin and hair development.

PLAU and SerpinB2 affect cell death differently in various forms of leprosy and could be targets for new treatments.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

Vav2 and Vav3 proteins help control skin stem cell numbers and activity in both healthy and cancerous cells.

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

Beta-catenin is crucial for skin cell growth, development, and cancer formation.

Increasing calcium sensing receptor speeds up skin and hair development in mice.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.