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Propranolol can cause reversible hair loss.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Not eating enough protein can cause hair roots to shrink and lose color, and hair to become thinner.

EGF and FGF help hair growth by affecting cell differentiation and fiber growth.

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

Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Edar signaling is crucial for proper hair follicle development and function.

Decomposed tritiated thymidine is less accurate for DNA tracing, and hair changes can indicate malnutrition.

Potassium levels affect blood sugar and insulin during dialysis, and malnutrition changes children's hair roots.

Some horses lose hair without inflammation or itching due to various conditions, and while mainly a cosmetic issue, diagnosis requires examination and biopsies, and breeding is not advised if it's hereditary.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Mice with human skin protein K8 had more skin problems and cancer.

Patient-derived melanocytes can potentially treat vitiligo by restoring skin pigmentation.

Six genetic conditions are often linked to complete scalp hair loss in children.

Hair loss has many causes and treatments, and losing some hair daily is normal; proper diagnosis is key, and minoxidil can help treat it.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

The document concludes that individualized treatments for hair issues are effective, certain hair changes can indicate neurocutaneous diseases, specific lotions improve skin health, laser hair removal works but needs more study on long-term effects, men's cosmetics are diverse, peeling is effective but can have side effects, and facial pigmentation is often due to overactive skin cells.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

MicroRNA-214 is important for skin and hair growth because it affects the Wnt pathway.

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

Cyclosporine A may help treat hair loss by blocking a protein that inhibits hair growth.

Assessing newborn scalp hair can reveal important health information.

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

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

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

The symposium concluded that hair growth involves complex processes, including the hair follicle life cycle, the role of the dermal papilla, hair strength, pigmentation, and the impact of diseases and treatments like minoxidil on hair and skin.