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AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Human liver cells stick to hair protein materials mainly through the liver's asialoglycoprotein receptor.

Female hair loss patients more likely to have dry eye and gland issues.

Certain skin cells near the base of hair muscles may help renew and stabilize skin, possibly affecting skin disorder understanding.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

The document says that there are treatments for hair and nail diseases.

Doctors should use a detailed patient history and physical exam to diagnose joint pain, and consult a rheumatologist early for suspected autoimmune diseases.

The review emphasizes the need to recognize skin conditions that affect hair follicles and sweat glands to avoid misdiagnosis.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

A medication may help with hair growth in psoriasis, and a skin condition might be linked to a specific bacteria.

Engineered skin substitutes can grow hair but have limitations like missing sebaceous glands and hair not breaking through the skin naturally.

Some alternative therapies for vitiligo show promise but need more research.

Videodermoscopy can help diagnose and monitor nail bed psoriasis.

Tiny pollution particles called PM2.5 can harm skin cells by causing stress, damage to cell parts, and cell death.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

Targeted cancer therapies often cause skin problems that need careful management to improve patient quality of life and treatment success.

Using 2% minoxidil for baldness treatment might cause vision distortion due to fluid build-up under the retina.

Most people with alopecia areata have nail changes, which are common but don't greatly affect their quality of life.

Different nail disorders are treated by targeting their specific causes and using appropriate medications or protective measures.

Despite progress in treatment, the exact cause of Alopecia areata is still unknown.

Higher antigliadin antibody levels are linked to alopecia areata severity.

Coating surfaces with human hair keratin improves the growth and consistency of important stem cells for medical use.

The study suggests that a new protease inhibitor can make hair harder to pull out, potentially reducing hair loss.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

Two-photon microscopy helps observe hair follicle stem cell behaviors in mice.

A new eyelid shampoo improved eyelid hygiene and eyelash length in people with Meibomian Gland Dysfunction.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Finasteride causes reduced tear flow and severe eye inflammation.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.