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Computational tools identified 29 drugs that could potentially target 19 genes involved in chemotherapy-induced hair loss, which could lead to more effective treatments.

Placenta extract in novasomes improved rat hair growth better than minoxidil and placenta extract in liposomes.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Jagged-1 in skin Tregs is crucial for timely wound healing by recruiting specific immune cells.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Androgen treatment with dihydrotestosterone may help maintain height in patients with 5-α-reductase type 2 deficiency, especially before puberty.

New treatments for hair loss could involve using stem cells and a process called the Wnt/beta-catenin pathway to stimulate hair growth.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

The tropical legume Sesbania rostrata can form nodules in waterlogged conditions using a different method that involves plant hormones and specific genes.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Skin cells show flexibility in healing wounds and forming tumors, with potential for treating hair disorders and chronic ulcers.

Special proteins are important for skin balance, healing, and aging, and affect skin stem cells.

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.

Zinc chloride can cause human scalp cells to multiply and die.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

Tea seed oil in nanostructured carriers stimulates hair growth and feels less greasy when applied.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

Hair loss in Androgenetic alopecia (AGA) is due to altered cell sensitivity to hormones, not increased hormone levels. Hair growth periods shorten over time, causing hair to become thinner and shorter. This is linked to miscommunication between cell pathways in hair follicles. There's also a change in gene expression related to blood vessels and cell growth in balding hair follicles. The exact molecular causes of AGA are still unclear.

Diagnosing and managing Glucocorticoid Resistance Syndrome is complex due to genetic differences and varied symptoms.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Alcohol-free minoxidil 5% is effective and safe for treating male pattern hair loss.

Studying rare genetic disorders can help us understand and treat common diseases better.

Addressing underrepresentation in Parkinson's research is crucial for better treatments and understanding.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

Skin aging is largely due to differences in stiffness and elasticity between skin layers, leading to wrinkles.

Existing drug dexamethasone may lower death risk in severe COVID-19 cases; more research needed for other drugs.

P144® improves hypertrophic scars by reducing size and thickness and increasing elasticity.