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Early onset hair loss linked to genetics and androgen levels.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

The method quickly analyzes hair growth genes and shows that blocking Smo in skin cells stops hair growth.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

The symposium highlighted the skin's role in sensing itch, pain, touch, and pleasure, and discussed new research and techniques for understanding and treating these sensations.

Skin's epithelial stem cells are crucial for repair and maintenance, and understanding them could improve treatments for skin problems.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Merkel cells stabilize nerve endings in the skin, and they change independently of each other.

Fat-related cells are important for initiating hair growth.

Macrophages are vital for skin healing, hair growth, salt balance, and cancer defense.

Certain variations in the vitamin D receptor gene are linked to an increased risk of polycystic ovary syndrome.

Neutrophil extracellular traps slow down hair follicle healing after injury.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Finasteride blocks progesterone's effect on absence seizures in rats.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

Different immune cells like platelets, mast cells, neutrophils, macrophages, T cells, B cells, and innate lymphoid cells all play roles in skin wound healing, but more research is needed due to inconsistent results and the complex nature of the immune response.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Wnt1/βcatenin signaling is crucial for heart repair after injury.

Hair loss needs more research for better treatments.

The Wnt/β-catenin pathway helps tissue regeneration but can also cause fibrosis, and drugs that inhibit this pathway may aid in healing skin and heart tissues.

Researchers created rat liver stem cells that could help repair liver failure in rats and may be useful for studying human liver diseases.

Ethylene and auxin hormones interact in complex ways that are essential for plant growth and development.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

Removing Dicer from pigment cells in newborn mice causes early hair graying and changes in cell migration molecules.