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The symposium concluded that hair growth involves complex processes, including the hair follicle life cycle, the role of the dermal papilla, hair strength, pigmentation, and the impact of diseases and treatments like minoxidil on hair and skin.

Beta-blockers and anti-anginal medications have various side effects and interactions that require careful monitoring and individualized treatment.

The CORIN gene variant causes the golden color in Siberian cats.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

Neurosteroids play a key role in controlling the brain-adrenal gland activity in pregnant sheep, both in normal and stressful situations.

A potential treatment for atopic dermatitis could be to increase PADI1 expression to improve skin barrier function.

Certain supplements, like whey protein isolate and growth hormones, can worsen hair loss.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Monoethanolamine-based hair colorants can cause more damage to hair than ammonia-based ones.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

AC5 improves hair loss and hair quality with high satisfaction rates.

Nanocarrier-based treatments show promise for better hair growth in androgenetic alopecia but need more research.

New treatment effectively reverses hair thinning in most patients with mild side effects.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Small proline-rich proteins and trichohyalin help make epithelial tissues tougher and more flexible.

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

Transamidases help form strong crosslinks in hair proteins, crucial for hair strength.

Excessive putrescine causes hair loss in transgenic mice by disrupting hair follicle development.

Significant progress was made in understanding PXE, but effective treatments are still needed.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

TGase 3 helps build hair structure by forming strong bonds between proteins.

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

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

Urinary Se to creatinine ratio, serum Se, and glutathione peroxidase are effective early biomarkers for selenium status in dogs.

Egyptian researchers are advancing in pharmaceutical nanotechnology, potentially improving health outcomes and the economy.

Enzymes called PADIs play a key role in hair growth and loss.

Genetic testing is crucial before giving azathioprine to avoid severe side effects.

Human hair loss may have evolved to help increase brain size.