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Men with baldness have higher levels of specific proteins, suggesting local hormone production may play a role in hair loss.

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

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Lack of cystatin M/E causes thin hair and dry skin.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Four genes affect hair follicle density in goats.

Finding functions for unknown GPCRs is hard but key for making new drugs.

Restoring skin bacteria may help reduce hair loss.

Exosomes from stem cells help hair regrowth by activating a specific signaling pathway.

Alk1 in specific cells is crucial for proper nerve branching and hair function.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between these conditions.

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

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

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

The research found that certain microRNAs are important for human hair growth and health.

Methylation in specific gene region causes finasteride resistance in some BPH patients.

EZH1 and EZH2 are crucial for healthy hair growth and skin repair.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

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

Hair follicle stem cells use specific chromatin changes to control their growth and differentiation.

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

Prolactin contributes to hair loss by promoting hair follicle shrinkage and cell death.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

CRISPR/Cas9 gene editing in cashmere goats increases hair follicles and fiber length, boosting cashmere yield.