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A compound from brown algae boosts the production of a certain inflammatory substance in skin cells.

Nicotinic acid reduces excessive oil production in skin cells by activating a specific receptor, which could help treat acne.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Scientists discovered a new way UVB light increases skin pigmentation through the ATP-P2X7 pathway.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Hair graying is caused by the loss of pigment cells due to poor maintenance of stem cells in the hair follicle.

Melatonin affects many body functions beyond sleep by interacting with specific receptors in various tissues.

Lactate production is important for activating hair growth stem cells.

Wnt ligands are crucial for hair growth and repair.

Male hormones and their receptors play a key role in hair loss and skin health, with potential new treatments being explored.

Androgenetic alopecia involves genetics, hormones, and can be treated with medications or surgery.

Blocking IL-12/IL-23p40 helped reverse severe hair loss in patients.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

ATP increases melanin production in skin after UV exposure, with the P2X7 receptor being crucial for this process.

The gel made of minoxidil and hydroxypropyl-β-cyclodextrin improves hair growth and is good for long-term use.

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

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

Melanocytes are crucial for skin pigmentation and can affect conditions like melanoma, vitiligo, and albinism, as well as hair color and hearing.

Scientists have created a new hair loss treatment using ultrasound to deliver gene-editing particles, which resulted in up to 90% hair regrowth in mice.

Mice with CBS deficiency are healthier on a low-methionine diet.

Autophagy is crucial for normal sebaceous gland function and sebum composition.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Tiny particles from skin cells can help activate hair growth.