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A new DSG4 gene mutation causes hair defects in a young girl.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Genomic prediction can improve breeding strategies for Korean Sapsaree dogs.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

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A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Sostdc1 controls the size and number of hair and mammary gland structures.

The UHS promoter is specific to mouse hair follicles.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

The correction does not change the conclusion that 2-deoxy-D-ribose helps hair regrowth.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Genetic differences affect breast cancer treatment success with tamoxifen in South African patients.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

New topical treatment using spherical nucleic acids shows promise in reducing psoriasis inflammation.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

OsPHR2 gene in rice enhances root growth and phosphorus accumulation.

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

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

UVB exposure affects retinoid metabolism, which is important for skin cancer progression and treatment.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

Promising cancer treatments were found, but the manufacturer closed.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Mutants of CYP154C2 enzyme significantly improved steroid conversion efficiency.

A 2-year-old girl had a hair disorder not shared by her identical twin.