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Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

Lack of functional CYLD in mice leads to early aging and cancer.

The side gland of Suncus murinus is a good model for studying human sebaceous glands.

The MtAnn3 gene affects root hair growth and is influenced by cytokinin.

CIPK13 and CIPK18 genes are crucial for root hair growth in plants.

Deleting Gpr54 speeds up hair growth and regeneration.

Researchers found specific genes in the part of hair follicles that could help treat hair disorders.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

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

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

The study developed a mouse model for Alopecia Areata that responds to treatment, useful for future research.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

Finding functions for unknown GPCRs is hard but key for making new drugs.

Male mice with FGF5 mutations grow longer hair than females.

CRISPR/Cas9 gene editing in cashmere goats increases hair follicles and fiber length, boosting cashmere yield.

Long non-coding RNAs play a key role in yak hair growth cycles.

Researchers created an efficient method to extract DNA from marmoset hair, avoiding blood chimerism.

Matriptase imbalance contributes to cancer development and spread.

The study concluded that the arachidonic acid pathway and the protein KRT79 play a role in determining the fineness of cashmere.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

GRK2 is essential for healthy hair follicle function, and its absence can lead to hair loss and cysts.

Mutant stem cells adapt their metabolism differently to outcompete normal cells in the skin.

The Itpr3 gene causes a specific hair pattern in mice.

Scientists found new and known long non-coding RNAs in mouse hair follicle stem cells that may be important for stem cell function and could be targets for cancer treatment.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

The KRTAP27-1 gene variations in sheep may affect wool length and weight.

High TSPEAR levels in colorectal cancer predict worse outcomes.