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Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Reduced matriptase activity causes skin and hair issues in both humans and mice.

The arrector pili muscle attaches to the extracellular matrix using α5β1 integrin and connects muscle cells using α1β1 integrin.

The inner root sheath evolved to help hair grow safely through the skin in mammals.

Type IV collagen chains vary in different parts of human skin, with specific patterns linked to melanocytes.

The atlas maps maize peptides, showing complex regulation and varied roles across tissues and stages.

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

The goat hair keratin gene is very similar to sheep's and is strongly expressed in goat hair follicles.

DNA methylation controls hair follicle gene expression in cashmere goats.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

Metabolic processes and key genes like FGF5, FGFR1, and RRAS significantly affect hair follicle growth in Inner Mongolian Cashmere goats.

The method shows how hair lipids form specific patterns and their roles in hair structure.

Two new gene mutations cause a rare hair disorder.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

Different types of inactive melanocyte stem cells exist with unique characteristics and potential to develop into other cells.

Junctional proteins stabilize the inner root sheath and connect the companion layer in human hair.

MicroRNA-200 prevents sebaceous gland development by inhibiting SOX9 and cell cycle progression.

Specific keratin gene mutations can cause monilethrix.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

QSOX enzymes help form protein bonds in cells, especially in tissues with high secretory activity.

Blocking TGFβ-RI signaling enhances surface ectoderm differentiation from human stem cells.

Hoxc13 gene expression and skin thickness change similarly during cashmere goat hair follicle development.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

The Eda gene helps regulate the hair cycle in goats.