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The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Mutations in the KRT16 gene can cause skin and nail disorders.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

Certain gene variations increase the risk of alopecia areata in Koreans.

Researchers found a new mutation causing total hair loss from birth.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

Mutant Cx43 causes slower wound healing and hair growth issues in ODDD.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

The research helps in creating genetically modified animals to study hair growth.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

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

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

Cyclic nucleotide-gated channels are crucial for proper root hair growth and calcium balance in plants.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

FGF13 gene changes cause excessive hair growth in a rare condition.