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The article concludes that the wool follicle is a valuable model for studying tissue interactions and has potential for genetic improvements in wool production.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

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

Alkaline Ceramidase 1 prevents early hair loss in mice by keeping hair follicle stem cells balanced.

Certain microRNAs are important for sheep hair follicle development and could help improve wool quality.

Nanocarriers with plant extracts show promise for safe and effective hair growth treatment.

Natural products show promise for new hair loss treatments.

New methods to test hair growth treatments have been developed.

RCM and OCT are effective for diagnosing and monitoring hair-related skin diseases but lack standardized protocols and need more research.

Blocking the mineralocorticoid receptor can help treat skin thinning caused by steroids.

Mouse models help understand alopecia areata and find treatments.

Researchers found 24 genes that change significantly and affect cashmere growth in goats; this could help increase cashmere production.

Some herbal ingredients like linalool and tea tree oil have anti-dandruff properties and are safe for use in shampoos.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

Excessive selenium from a supplement caused toxicity but patients recovered with care.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Signals from skin cells controlled by Rac proteins help turn certain precursor cells into white fat cells.

The document is a detailed guide on skin conditions and treatments for dermatologists.

The study concluded that people with Lichen Planopilaris have a more diverse scalp bacteria and different metabolic pathways compared to healthy individuals.

The study concluded that the arachidonic acid pathway and the protein KRT79 play a role in determining the fineness of cashmere.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

Many alopecia patients have undetected thyroid abnormalities that can be found through physical exams.

The document concludes that immune system abnormalities cause alopecia areata, but the exact process is still not completely understood.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Gamma-ray exposure can cause long-lasting damage to hair follicles, affecting hair structure and color.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.