Search

everythinglearnresearchcommunity

for

Search:↓

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

Hedgehog signaling is crucial for hair development, cadherins affect cell adhesion, neutrophils play a role in skin lesions, and BP230 autoantibodies impact skin stability.

Ornithine decarboxylase is crucial for human hair growth and the hair cycle.

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

The study created hair-bearing skin models that lack a key protein for skin layer attachment, limiting their use for certain skin disease research.

Hair loss is caused by the breakdown of a protein called COL17A1 in hair follicle stem cells.

Most patients with autoimmune blistering diseases experienced some hair loss, which may be underreported and linked to disease severity.

Panitumumab treatment can cause unusual hair growth in some colorectal cancer patients.

pCLCA2 protein may help maintain skin structure and function.

miR-182 may help treat hallux valgus by targeting FGF9.

FOL-005 peptide can reduce human hair growth by lowering FGF7 levels.

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

KRTAP28-1 gene can help breed sheep with finer wool.

Cells from certain embryo parts can induce head formation in another embryo, involving complex signaling pathways.

Exosomal miR-199a-3p from dermal papilla cells helps control hair color by affecting melanocytes.

Certain genetic markers may increase or decrease prostate cancer risk.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

FOL-026 peptide may help hair growth and cardiovascular health by improving blood flow and cell functions.

KRT72 gene helps form hair.

A rare case of a transplant patient developing a skin condition linked to HPV-49.

E6/E7 oncogenes in hair follicles cause continuous hair growth by skipping the resting phase.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Markers CRABP1, Nestin, and Ephrin B2 are present in skin cancer environments and may influence their development.

Forensic DNA phenotyping can now predict more physical traits and ancestry from DNA, but further improvements are needed.

IGFBP-rP1 could be a new treatment for a common type of hair loss.