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Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

Sensory neuron remodeling and Merkel-cell changes happen independently during skin maintenance.

Sensory neuron changes and Merkel-cell changes in the skin happen independently during normal skin maintenance.

Sensory neuron and Merkel cell changes in the skin happen independently during normal skin maintenance.

Sensory neurons and Merkel cells remodel at different rates during normal skin maintenance.

Sensory neuron remodeling and Merkel-cell changes in the skin happen independently.

Sensory neuron and Merkel-cell changes in the skin happen independently during normal skin maintenance.

Sensory neuron and Merkel cell changes in the skin happen independently during normal skin maintenance.

Six genetic conditions are often linked to complete scalp hair loss in children.

miR-29a-5p prevents the formation of early hair structures by targeting a gene important for hair growth and is regulated by a complex network involving lncRNA627.1.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

Toothpaste containing α-tocopherol acetate, l-menthol, and stevioside can promote hair growth in mice.

Different types of sun exposure damage skin cells and immune cells, with chronic exposure leading to more severe and lasting damage.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

New technologies show promise in healing wounds, treating cancer, autoimmune diseases, and genetic disorders.

The Notch signaling pathway is important for hair follicle development and could help create treatments for hair disorders.

Understanding hair follicle communication can help treat hair loss.

Monilethrix causes fragile, patchy hair loss.

The CTLA-4 gene polymorphism does not affect polycystic ovarian syndrome.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

A specific gene mutation causes different hair defects in Indian monilethrix families.

An allele of the KRTAP13-2 gene may improve wool quality in sheep.

Krox20 (Egr2) is important for the function of epithelial stem cells.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

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

KRTAP10 proteins help form the hair shaft's tough outer layer by interacting with specific hair keratins.

A rabbit gene important for hair development was identified and detailed.