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IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

Specific keratin gene mutations can cause monilethrix.

Reflectance confocal microscopy can noninvasively diagnose onychomatricoma by showing unique features different from healthy nails or nail fungus.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Epidermal growth factor disrupts hair and gland formation in bandicoots.

Single Blimp1+ cells can create functional sebaceous gland organoids in the lab.

A 29-year-old man had a jaw plaque diagnosed as follicular mucinosis, linked to nestin-positive hair follicle stem cells.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

Id proteins, especially Id2 and Id3, are crucial for hair follicle development and stem cell regulation.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

Special astroglia cells improved stroke recovery in rats, a hair growth drug reduced cancer spread, and tiny magnesium structures were more easily shaped.

The mineralocorticoid receptor temporarily affects mouse skin development, but the glucocorticoid receptor has a more lasting impact.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

GIANT improves brain imaging by using genetics to better map brain regions.

Deleting MPZL3 increases skin oil production and reduces body fat.

High levels of 3 alpha-diol glucuronide in the blood are a marker of increased androgen action in women with excessive hair growth of unknown cause.

During late pregnancy in rats, hormonal changes increased certain GABAA receptors in specific brain cells.

miR-325-3p can slow down brain tumor growth by targeting FOXM1.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Ca²⁺-mediated protein citrullination controls cell growth in the CNS and may help treat brain tumors.

A gene mutation in mice causes skin defects and early death.

TGF-beta 1 and IGF-II mRNA have specific patterns in pig subcutaneous tissue, affecting fat and muscle development.

A new diagnostic model can help better diagnose and understand Alopecia Areata.

Enhanced stem cells from the placenta can reduce fat buildup in eye tissue for Graves' disease.

A new test more accurately detects citrulline in hair follicles and pilomatrixomas.