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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.

Nanoliposomes effectively deliver hair-growth peptides into hair follicles.

Different genes are linked to various types of hair loss.

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.

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.

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

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

ASH2L is essential for skin and hair development.

Hair loss caused by genetics and hormones; more research needed for treatments.

Human fetal placental stromal cell injections speed up healing and improve skin and hair recovery after radiation damage.

A man had a large, rare cyst in his mouth removed after 10 years, which fixed his swallowing and breathing problems.

The document concludes that while there are various treatments for Alopecia Areata, there is no cure, and individualized treatment plans are essential due to varying effectiveness.

The three estrogen receptor genes are highly expressed in zebrafish neuromasts during development.

Hair and skin can regenerate without bulge stem cells due to other compensating cells.

Substances from dental stem cells might help treat hair loss.

Some hair protein genes evolved early and were adapted for use in hair follicles.

NF-κB is crucial for different stages and types of hair growth in mice.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.