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Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.

A new mutation in the HR gene causes hair loss in a specific family.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

PEA boosts allopregnanolone production and reduces oxidative stress in brain cells.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Pemigatinib may be effective for treating ZMYM2::FGFR1 fusion-positive leukemia.

Spiny mice have resilient, large mitochondria that help them regenerate tissue.

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

Homozygous K5Cre transgenic mice have wavy hair and faster cancer progression.

The N gene affects the protein makeup of mouse hair.

ALRN-6924 may prevent hair loss caused by chemotherapy.

The fuzzy gene is crucial for controlling hair growth cycles.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

The Celsr1 gene is crucial for normal hair patterning in mice.

Modified pep7, named EPM peptide, effectively promotes hair growth at low concentrations and works well with minoxidil.

A new compound slows cancer cell growth and causes cell death by blocking cell cycle progression and increasing cell-damaging molecules.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

Wnt ligands, produced by dermal papilla cells, are essential for adult hair growth and regeneration.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

A mother's PPARγ is crucial for preventing harmful milk that can cause inflammation and growth problems in babies.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

Activating Kras in mouse skin causes excess skin and hair loss.