Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

A new compound, HTPI, promotes hair growth by protecting cells from damage and regulating energy use.

Hyaluronan from Has2 is important for proper wound healing and hair follicle development.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

T cells show stress responses in alopecia areata, suggesting potential treatment targets.

Prostaglandin E2 helps prevent hair loss from radiotherapy by protecting hair growth cells and aiding self-repair.

Hairless gene not strongly linked to baldness.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

The study found that women with hyperandrogenic PCOS have higher levels of AKT1 and AKT2 proteins in their cells, which may lead to cell dysfunction.

Immune activities and specific genes are important in male pattern baldness.

Using hemocoagulase with platelet-rich plasma in hip replacement can lessen blood loss and improve healing and blood clotting.

BST2 is highly expressed in certain immune cells in alopecia areata, suggesting a role in the disease.

Sox2-positive dermal papilla cells have unique characteristics and contribute more to skin and hair follicle formation than Sox2-negative cells.

Skin cells and certain hair follicle areas produce hemoglobin, which may help protect against oxidative stress like UV damage.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

Tanning ability is linked to specific DNA changes in skin genes.

Two main types of fibroblasts with unique functions and additional subtypes were identified in human skin.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

Changes in genes FGA, VWF, and ACTG1 may contribute to pemphigus vulgaris.

Ghrelin and its receptors likely aren't risk factors for PCOS.

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

Human pluripotent stem cells could be used to make platelets for medical use, but safety, effectiveness, and cost issues need to be resolved.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

TCHHL1 is a protein important for hair growth, found in hair follicles.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

miR-200c-3p could help diagnose and treat alopecia areata.