Search

everythinglearnresearchcommunity

for

Search:↓

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

Secukinumab treatment may cause HBV reactivation and hair discoloration.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Targeting protein S-palmitoylation could lead to new skin disease treatments.

A new portable microscope can effectively monitor skin wound healing in real-time.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

DHCer levels in hair could be a biomarker for alopecia progression.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Scientists found out how a specific protein in human hair cuticles behaves and is structured.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new enzyme, BSSP, is found in high amounts in the hair follicles of nude mice.

PBX1 reduces aging and cell death in stem cells by boosting SIRT1 and lowering PARP1.

PPARγ signaling modulation can protect hair follicle stem cells from chemotherapy-induced damage.

Lichen planus pigmentosus may indicate undetected hepatitis C infection.

The method accurately measures finasteride in capsules.

Povidone iodine reduced skin bacteria more than chlorhexidine gluconate, but neither met FDA reduction standards.

Polygenic Score can help predict severe psoriasis and psoriatic arthritis.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Bleach baths with 0.005% hypochlorite help manage atopic dermatitis by affecting skin cells and reducing itchiness.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

A fragment of human type XVII collagen shows great potential for skin health and wound healing.

A woman with a skin disorder was found to have hepatitis C, which may be linked, and was safely treated with methotrexate.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

A woman's psoriasis improved after hepatitis C treatment with interferon, despite interferon's risk of worsening skin conditions.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

The document's content couldn't be processed.

HPV-150 and HPV-151 are rare skin viruses linked to warts and some skin cancers.