Search

everythinglearnresearchcommunity

for

Search:↓

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

Human placenta extract reduces inflammation and symptoms in atopic dermatitis.

Transcutaneous vaccination using nanoparticles can enhance immune responses and reduce basal cell carcinomas.

Human hair follicle stem cells can become smooth muscle cells using specific growth factors.

Researchers found that hair follicle stem cells can become squamous cell carcinoma due to Ras activation, which could lead to new treatments.

Mouse hair follicle stem cells have a flexible chromatin state that supports skin health and hair growth.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

Certain HLA class II alleles increase or decrease the risk of alopecia areata.

Different types of hidradenitis suppurativa need specific treatments based on unique skin cell issues.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

A specific gene mutation causes woolly hair and hair loss.

Mutations in the Whn gene affect hair keratin gene expression differently.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

Proper hedgehog signaling is crucial for maintaining healthy skin stem cells.

miR-124 helps mouse hair follicle stem cells become nerve cells by blocking Ptbp1 and Sox9.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

A peptide from hair follicle stem cells can boost hair growth.

CARASIL can cause different symptoms even with the same genetic mutation.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

Nonmelanoma skin cancers have higher levels of certain osteopontin variants than normal skin.

Targeting impaired Nrf2 signaling might help treat hidradenitis suppurativa early on.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

A rare neck cyst in a 47-year-old man showed diverse skin cell types and was not linked to HPV.