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The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Dogs could be good models for studying human hair growth and hair loss.

Certain human skin cells marked by CD44 and ALDH are rich in stem cells capable of long-term skin renewal.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

The review found that different stem cell types in the skin are crucial for repair and could help treat skin diseases and cancer.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

Finasteride reverses early hair loss and promotes growth.

Stem cell differentiation is crucial for skin barrier maintenance and its disruption can lead to skin diseases.

EPR spectroscopy showed that spontaneous hair growth results in thicker skin and less pigmented hair than depilation-induced growth.

Alfredo Rebora suggested a new, easier way to classify hair loss in Telogen Effluvium, adding a type possibly related to autoimmune diseases.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Cell therapy shows promise for treating severe psoriasis but needs more research to confirm safety and effectiveness.

The method increases stem-like cells for better skin regeneration.

Hair casts on the scalp may be a sign of ongoing pemphigus vulgaris and could suggest a need to adjust treatment.

Trichoscopy helps quickly identify autoimmune diseases on the scalp but should be used with other standard tests.

Hair loss in autoimmune blistering skin diseases varies and may regrow with disease control.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

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

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

An 18-year-old girl with pemphigus vulgaris needed strong medication and careful treatment due to ineffective initial therapies and side effects.

The girl's regrown brown hair had less of certain pigments than her original black hair.

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

Melanocytes are diverse cells important for pigmentation and skin health, influenced by genetics and environment.

Hair loss can indicate or worsen with systemic diseases, and treating the underlying condition is important.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

No link found between Coxsackie viruses and pemphigus.