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

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

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

CD201+ fascia progenitors are essential for wound healing and could be targeted for treating skin conditions.

Oral zinc therapy is effective for treating acrodermatitis enteropathica.

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

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

Hair follicle stem cells use specific chromatin changes to control their growth and differentiation.

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

EDA2R gene linked to hair loss.

Melanocyte development from neural crest cells is complex and influenced by many factors, and better understanding could help treat skin disorders.

There are still challenges in diagnosing and treating chronic skin diseases, but there is hope for future improvements.

New genes found linked to balding, may help develop future treatments.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

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

Blocking the prolactin receptor might help treat various diseases, but more research is needed.

The protein SLC1A3 is important for activating skin stem cells and is necessary for normal hair and skin growth in mice.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

No link found between new male baldness genes and female hair loss.

Whale genes show changes that help them live in water, like less hair and better flippers.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

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

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

The transition from growth to regression in Cashmere goat hair follicles involves changes in expression of genes related to keratin and cell differentiation.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.