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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

PDRN helps repair tissue and improve wound healing with a high safety profile.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

A new gene mutation linked to a skin condition was found in a Spanish family.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

miRNAs in the Dlk1-Gtl2 region may improve lamb fur quality.

Acute stress increases Y1 receptor gene expression in certain brain areas, but repeated stress does not.

Finasteride effectively inhibits the enzyme steroid 5 alpha-reductase II.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

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

MK-0773 is a moderate inhibitor of the SRD5A2 enzyme.

Mice genetically modified to produce more Del1 protein had faster hair regrowth.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Trps1 is essential for proper hair follicle development.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

The research gives new understanding on how human steroid 5α-reductases work and how drugs like finasteride inhibit them, which could help in creating new drugs.

Finasteride reduces certain behaviors caused by D1-like receptor agonists but not by D2-like receptor agonists in mice.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

FOXN1 gene variants cause low T cells and immune issues from birth.

Dynlt3 is important for melanosome transport and skin coloration.

Orai1 protein is crucial for tooth development and affects enamel thickness and mineralization.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Nocturnal calcium infusions improved a boy's severe rickets without causing hair loss.