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Activating mitophagy may help manage a key immune response involved in the hair loss condition alopecia areata.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Nitrate helps plants manage phosphate uptake and starvation responses through NIGT1 proteins.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

CRH causes hair loss by reducing autophagy and increasing cell death in hair cells.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

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

Removing Mediator 1 from certain mouse cells causes teeth to grow hair instead of enamel.

MPZL3 protein affects hair growth cycles and could help manage hair loss.

Reducing PIEZO1 speeds up wound healing.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Newly designed proteins can effectively degrade specific proteins in cells, offering a promising alternative for targeted protein degradation.

Reducing Tyrosinase prevents mature color pigment cells from forming in mouse hair.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

MPZL3 protein is important for controlling hair growth cycles.

Scientists can control how skin stem cells divide by using different treatments.

NEDD4 and NEDD4L help control intestinal stem cells and prevent tumors by breaking down the LGR5 receptor.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Sgk3 is essential for normal hair follicle growth and maintenance.

Wnt signaling is vital for cell growth, development, and cancer research.

Mitochondrial problems in tooth cells lead to bad enamel and dentin development in mice.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.