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Combining PRP with lipofilling shows promise for tissue regeneration but needs more clinical trials to confirm benefits.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

GFP transgenic mice help study cell origins in skin grafts.

Controlling Tslp can improve health in AEC syndrome patients.

mTORC1 activity is important for hair growth and color, and targeting it could help treat hair loss and greying.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

Nanoliposomes effectively deliver hair-growth peptides into hair follicles.

A peptide called DPS-1 helps human scalp cells grow and stimulates hair growth in mice.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Different genes are linked to various types of hair loss.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Intense Pulse Light effectively reduces hair growth in faun tail nevus.

Removing p16INK4a from skin cells can lead to faster and more clumped growth, which might help with hair growth.

Ectodysplasin signaling is crucial for skin appendage development, requiring specific doses and durations.

Growth factors greatly affect hair loss, with different levels seen in men, women, younger patients, and at the start of the condition.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Most skin tumors in the study were benign, with squamous cell carcinoma being the most common malignant type.

Teratoma hair is similar to scalp hair but has a rougher surface and lower adhesive force.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

Estrogen replacement can improve skin health in menopausal women but doesn't reverse sun damage or prevent hair loss.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.