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A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

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

People often underestimate hair loss severity, with fewer seeking treatment, and it's more distressing for women.

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

The meeting presented new findings on hair stem cells, pigmentation, genetics, and modern hair treatment techniques.

Plant roots respond to fungus smells by possibly using certain proteins and a plant hormone to change root growth, but more research is needed.

Different fish use the same genes to regrow teeth.

New technologies show promise in healing wounds, treating cancer, autoimmune diseases, and genetic disorders.

Hair loss caused by genetics and hormones; more research needed for treatments.

Auxin and ethylene hormones both work together and against each other to control plant growth.

Wnt signaling is crucial for pigmented hair regeneration by controlling stem cell activation and differentiation.

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

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

Scientists turned mouse stem cells into skin cells that can grow into skin layers and structures.

5α-reductase is essential for male sexual development and its inhibitors have potential in treating various conditions related to hormone action.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

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

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Hormones during pregnancy and lactation keep skin stem cells inactive, preventing hair growth.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

Researchers found a new mutation causing total hair loss from birth.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Researchers found a gene mutation responsible for a rare hair loss condition.

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