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TPA strongly increases ODC activity in certain skin cells, potentially aiding tumor growth.

A fungal enzyme was used to make compounds more soluble, aiding drug discovery and crop protection.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

New genetic insights have improved understanding of hair loss, leading to a new test and treatments, but more research is needed on the test and laser comb effectiveness.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Linear lichen planopilaris can affect the trunk, not just the face.

Using bioreactors, scientists can grow more skin stem cells that keep their ability to regenerate skin and hair.

Keratins are crucial for hair strength, and mutations in certain keratin genes cause hair disorders.

A two-step method was created in 2015 to make more cells that help with hair growth, but they need to be combined with other cells for 4 days to actually form new hair.

A new method was developed to grow and maintain human hair follicle stem cells for hair reconstruction.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Scientists can grow human hair follicle stem cells in a lab without changing their nature, which could help treat hair loss.

Human epidermal neural crest stem cells could be used for therapies, drug discovery, and disease modeling.

A dog's skin calcification condition resolved without treatment after a bacterial infection.

A new patch can deliver stable antibodies over time for potential HIV treatment.

Scientists made stem cells that can grow hair by adding three specific factors to them.

Platelet-rich fibrin (PRF) is better for natural healing, especially in dental and medical treatments.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Two cows had a rare hair disorder causing hair loss but were otherwise healthy.

Mesenchymal stromal cell therapies show promise for treating various diseases but need more research and standardization.

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

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

Different problems with hair stem cell renewal can lead to hair loss.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.