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A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Wnt10b promotes hair growth, while SFRP2 inhibits it in Wanxi Angora rabbits.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Blocking GPR91 can help prevent and reverse hair loss in androgenetic alopecia.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

Different forms of FGF5 either promote or inhibit hair growth.

Researchers identified genes that may affect hair growth in Cashmere goats.

The hexosamine pathway helps protect skin cells from stress and may improve skin and hair health.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

miR-200c-3p could help diagnose and treat alopecia areata.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

FOXC1 boosts SFRP1 in hair loss, suggesting new treatments.

Recent selection on immune response genes was identified across seven ethnicities.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

Aminoguanidine increases VEGF in stored hair micrografts, potentially improving their viability after transplant.

A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

The GG genotype of the KRT71 gene leads to longer wool in Gansu alpine fine-wool sheep.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.