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

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Dihydrotestosterone changes some hormone-related gene expressions in rat pituitary glands but doesn't affect the estrous cycle.

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

Planarian regeneration begins with a specific gene activation caused by injury, essential for healing and tissue regrowth.

Cathepsin L is essential for normal hair growth and development.

A new protein was made to detect specific skin cell growth receptors and worked in normal skin but not in skin cancer cells.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

The study concludes that the EDA2R gene is activated by p53 during chemotherapy but is not necessary for chemotherapy-induced hair loss.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

No CD44 in alopecia areata, present in normal and androgenetic alopecia.

Chronic stress in mice changes skin metabolism and gene expression, leading to hair loss.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

SOX9 helps determine stem cell roles by interacting with DNA and proteins that control gene activity.

Hair growth genes work better with more glucose due to changes in gene-regulating markers.

Hairless protein is key for hair growth, cell differences cause gene expression variation, and the N-end rule pathway senses nitric oxide for protein breakdown.

Gata6 is important for protecting hair growth cells from DNA damage and keeping normal hair growth.

Some growth factors, while important for normal body functions, can cause diseases when not regulated properly.

Scientists created keratinocyte cell lines from human hair that can differentiate similarly to normal skin cells, offering a new way to study skin biology and diseases.

Two compounds from Asiasarum heterotropoides roots show potential as lung cancer treatments without harming normal cells.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.