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A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Targeting FGF5 could help treat prostate cancer.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

BcFLA1 protein is crucial for root hair growth in response to low phosphate in Brassica carinata.

A young cat had a rare fungal infection caused by Microsporum gypseum.

A small group of slow-growing cells causes basal cell carcinoma to return after treatment.

Different γδ T cell types have unique roles in causing alopecia areata.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

PAR-1 may play a role in hair growth regulation in human hair follicles.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

Tyrosinase and gp100 proteins can help diagnose and treat melanoma.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

CE-PTG is a better method for analyzing hair growth in androgenetic alopecia.

Pyoderma gangrenosum can occur in rheumatoid arthritis patients and may be mistaken for vasculitis.

High ODC and low K1 and K10 may indicate early skin tumors in mice.

Protein Kinase C shows promise for cancer treatment, but more research is needed to develop effective inhibitors.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

The CUBIC protocol allows detailed 3D visualization of proteins in mouse skin biopsies.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Foreskin keratinocytes and SVK14 cells express certain cytochrome P450 enzymes, unlike hair follicle keratinocytes.

Patients need better information about the risks of long-term steroid use.

A mouse model for studying scleroderma in chronic graft-versus-host disease was successfully created.