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The secretome from mesenchymal stem cells is a promising treatment that may repair tissue and avoid side effects of stem cell transplantation.

The hedgehog signaling pathway is crucial for hair growth but not for the initial creation of hair follicles.

Understanding hair growth involves complex interactions between molecules and could help treat hair disorders.

Estrogen replacement can improve skin health in menopausal women but doesn't reverse sun damage or prevent hair loss.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Growth factors are crucial for hair development and could help treat hair diseases.

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

EGF and KGF signalling prevent hair follicle formation and promote skin cell development in mice.

Follistatin helps hair growth and cycling, while activin prevents it.

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.

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.

Researchers found a way to create cells from stem cells that act like human cells important for hair growth and could be used for hair regeneration treatments.

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.

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.

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

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

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.