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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

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

UC.145 may be a new biomarker for predicting gastric cancer.

Overexpression of LRIG3 in skin causes hair loss.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

Hoxc genes control hair growth through Wnt signaling.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Progerin affects cell shape but not hair or skin in mice.

LGR5 and LGR6 are expressed differently in various skin tumors, which may offer clues about their origins.

H19 may help cause PCOS by affecting CTGF levels, suggesting a new treatment target.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

Mutations in the HOXC13 gene cause hair and nail development issues.

The E2 protein affects gene activity in hair follicles of mice.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.

A truncated protein linked to breast cancer may change cell adhesion.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A specific DNA region controls skin cell gene expression by working with certain proteins.

The hairless protein is important for skin, hair, and may influence cancer development.

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Removing GRK2 in skin cells causes hair loss similar to immune-related alopecia.

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

Vitamin D receptor and hairless protein are essential for hair growth.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Hhip-Cre effectively targets dermal papilla cells for gene manipulation in hair biology.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.