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Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Mice lacking a key DNA methylation enzyme in skin cells have a lower chance of activating stem cells necessary for hair growth, leading to progressive hair loss.

Blocking BMP signaling causes hair loss and disrupts hair growth cycles.

The guide explains how to identify and treat children's hair loss, including fungal infections, autoimmune disorders, hairstyle changes, self-correcting conditions, and behavioral therapy for hair-pulling.

Researchers created hair-inducing human cell clusters using a 3D culture method.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Tiny particles called extracellular vesicles could help with skin healing and hair growth, but more research is needed.

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

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

Nanoencapsulation creates adjustable cell clusters for hair growth.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Some families have a genetic condition where they are born with irregular scalp defects.

DNA methylation changes are linked to hair growth cycles in goats.

Loose Anagen Syndrome causes easy-to-pull, thin hair, mainly in young girls, and improves with age.

Gene network oscillations inside hair stem cells are key for hair growth regulation and could help treat hair loss.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

Aging scalp skin contributes to hair aging and loss, and more research is needed to develop better hair loss treatments.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

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

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

Women experience various skin issues at different life stages, requiring careful treatment and awareness.

Scube3 gene affects mouse embryo growth in multiple areas, but needs more research.

The document concludes that certain chemicals can help maintain stem cell pluripotency and that understanding cell states is crucial for tissue regeneration.

Leg hair can be used for eyelash transplants, resulting in fuller lashes with less maintenance.

The PP2A-B55α protein is essential for brain and skin development in embryos.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.