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Understanding proteins in skin structures like claws and hair is crucial for future research.

Mesenchymal stem cell proteins in a special gel improved healing of severe burns.

Caspases are enzymes important for both cell death and various non-lethal cell functions, affecting head development and hair growth, with different caspases playing specific roles.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Different types of cell death affect skin health and inflammation, and understanding them could improve treatments for skin diseases.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

After skin is damaged, noncoding dsRNA helps prostaglandins and Wnts work together to repair tissue and promote hair growth.

New treatments for skin damage from UV light using stem cells and their secretions show promise for skin repair without major risks.

Acetylcholine receptors might be involved in the development of acne inversa and smoking could worsen the condition.

Skin aging is a complex process influenced by various factors, leading to wrinkles and sagging, and should be considered a disease due to its health impacts.

Trichohyalin-like proteins are essential for the development of skin structures like hair, nails, and feathers.

The right amount of retinoic acid is essential for normal hair growth and development.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

Transglutaminase activity is important for skin and is found in both mammals and birds.

Mast cells and CD8 T cells interact closely in skin diseases, affecting each other's behavior and contributing to conditions like psoriasis and eczema.

Sunlight exposure damages hair follicles, but certain stem cell-derived particles can reduce this damage and help with hair regeneration.

Melatonin, a hormone, can help protect skin from aging by reducing stress, inflammation, and damage, and may also help treat hair loss in women.

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

Exosomes show promise for improving wound healing, reducing aging signs, preventing hair loss, and lightening skin but require more research and better production methods.

Silencing certain circadian clock genes increases skin pigmentation.

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

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.

EGFR and mTOR inhibitors may help manage Olmsted syndrome symptoms.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

FA2H is essential for normal fur and sebum production in mice.

Knowing how skin works and its diseases helps doctors diagnose and treat skin conditions better.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

Murine hair has specific types of ceramides and glucosylceramides but lacks acylceramides.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.