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Blocking androgen receptors early in life increases estrogen levels and reduces sexual motivation in male rats.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

BLMP-1 is important for regular molting and gene expression cycles in worms.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

IGN genes may regulate hair growth and could be targeted for hair-loss treatments.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

EBF1 controls hair type and length.

A low-protein diet with methionine is cost-effective and supports normal growth and high-quality pelts in blue foxes.

5% topical minoxidil improves hair density and quality in monilethrix patients.

The OVOL1 gene, controlled by β-catenin, is crucial for creating hair follicles.

Lack of KSR1 stops certain skin tumors in mice.

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

γδ T cells help with hair growth during wound healing in mice.

Wnt/beta-catenin signaling in the skin helps fat cell development during hair growth and repair.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

ocu-miR-205 affects hair density in Rex rabbits by altering hair follicle growth and signaling pathways.

UTX is crucial for skin differentiation and health, especially in females.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

The Hairless gene is crucial for hair cell development, affecting whether skin cells become hair or skin and oil gland cells.

Plerixafor may help treat pigmentation disorders by promoting skin repigmentation.

A new mouse model helps study melanocyte cells using GFP expression.

Nerve cells and other cell types work together to start horn growth in dairy goats.

Hairlessness in mammals is caused by combined changes in genes and regulatory regions.

The type of tumor suppressor affects the form of skin cancer from hair follicle stem cells.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Removing PLCg1 from skin cells caused thicker oil glands and less hair in mice.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.