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Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Cutaneous Lymphadenoma is a unique skin tumor with specific protein markers and common gene mutations that may cause continuous cell growth.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

Double-stranded RNA causes inflammation in hair follicle cells, which may help understand and treat alopecia areata.

The research identified genes that explain why some sheep have curly wool and others have straight wool.

The research identified key molecules that help hair matrix and dermal papilla cells communicate and influence hair growth in cashmere goats.

Certain herbal compounds might help prevent hair loss in menopausal women by activating Vitamin D receptors.

Both classical and L-type atypical BSE from cattle can infect goats with different incubation times, and tests can distinguish between the two strains.

Basal cell carcinomas may differentiate similarly to hair follicles and could be influenced by hair cycle-related treatments.

Trichloroethylene causes skin inflammation in mice by increasing certain immune proteins.

Prolactin slows down hair growth in mice.

LGR5 helps maintain corneal cell characteristics and prevents unwanted changes by controlling specific cell signaling pathways.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

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

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

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

Notch1 signaling is crucial for improving wound healing and skin regeneration by affecting stem cell behavior.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

TLR2 is important for hair growth and can be targeted to treat hair loss.

TLR3 signaling enhances the immunosuppressive properties of human periodontal ligament stem cells.

Mice without Vitamin D receptors have hair growth problems because of issues in the hedgehog signaling pathway.

The Wnt/β-catenin pathway can activate melanocyte stem cells and may help regenerate hair follicles.

GLI2 increases follistatin production in human skin cells.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

The shape of fibrous scaffolds can improve how stem cells help heal skin.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

Chitosan/LiCl composite scaffolds help heal deep skin wounds better.