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Different Myc family proteins are located in various parts of the hair follicle and may affect stem cell behavior.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Human Schwann cells can be quickly made from hair follicle stem cells for nerve repair.

3,4,5-tri-O-caffeoylquinic acid promotes hair growth by activating the β-catenin pathway.

A form of vitamin E promotes hair growth by activating a specific skin pathway.

Bezafibrate treatment improved skin and spleen health in aging mice but didn't extend lifespan.

Blocking the Wnt/β‐catenin pathway can speed up wound healing, reduce scarring, and improve cartilage repair.

Deleting MED1 in skin cells causes hair loss and skin changes.

Neuregulin3 affects cell development in the skin and mammary glands.

SIRT7 protein is crucial for starting hair growth in mice.

Two new compounds were found to build bone and muscle without affecting reproductive organs and skin oil glands.

Stem cells can help other stem cells by producing supportive factors.

Melanocyte stem cells are crucial for skin pigmentation and have potential in disease modeling and regenerative medicine.

Miz1 is essential for proper hair structure and growth.

The conclusion is that understanding how hair follicle stem cells live or die is important for maintaining healthy tissue and repairing injuries, and could help treat hair loss, but there are still challenges to overcome.

ACBP is crucial for healthy skin in mice.

Low selenium levels can extend lifespan but worsen health issues.

Five preservatives may disrupt hormone function and need more health and environmental risk assessment.

The Msi2 protein helps keep hair follicle stem cells inactive, controlling hair growth and regeneration.

VDR regulation varies by tissue and is crucial for its biological functions.

Natural small molecules can help treat diseases by activating or inhibiting the Wnt pathway.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Zebrafish need MYC and FGF to regenerate inner ear hair cells.

Testosterone therapy helps boys with hormone deficiencies develop normal male characteristics and grow properly.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Managing oxidative stress might help treat low testosterone and related chronic diseases in aging men.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

As skin cells mature, vitamin D receptor levels decrease while retinoid X receptor α levels increase.