Search

everythinglearnresearchcommunity

for

Search:↓

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

Epidermolysis bullosa is an inherited condition causing fragile skin with no cure, managed by wound care and experimental treatments show promise.

The skin's basement membrane has specialized structures and molecules for different tissue interactions, important for hair growth and attachment.

The document concludes that the technique allows for the detection of LDH activity in various tissues, showing where cells are actively metabolizing glucose.

The skin's basement membrane is specially designed to support different types of connections between skin layers and hair follicles.

The document concludes that accurate diagnosis of different types of hair loss requires careful examination of hair and scalp tissue, considering both clinical and microscopic features.

Trichohyalin is also found in the outer layers of normal human skin.

The guide explains how to study human skin fat cells and their tissue, aiming to improve research and medical treatments.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

Correct skin biopsy techniques are crucial to avoid misdiagnosis of skin diseases.

The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

VDUP1 is found in skin and hair follicles, interacts with sciellin, and may help regulate skin cell differentiation.

Age-related hair loss is linked to the decline and dysfunction of hair follicle stem cells.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Shi-Bi-Man activates hair follicle stem cells and promotes hair growth by changing lactic acid metabolism and other cellular processes.

Negative pressure therapy increases hair growth in mice.

Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

The document suggests that severe hair loss in SLE patients may be an early sign of scalp DLE, treatable with immunosuppressive therapy.

The method allows for 3D tracking of hair follicle stem cells and shows they can regenerate hair for up to 180 days.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

Hair follicle dermal stem cells are key for regenerating parts of the hair follicle and determining hair type.

The study found that two enzymes linked to hair loss are located in different parts of the scalp, supporting a common treatment's effectiveness.

Minoxidil helps hair growth by activating the β-catenin pathway.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Human alpha defensin 5 helps heal wounds, reduce bacteria, and grow hair on burned skin.