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A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Erythropoietin overexpression disrupts hair growth and fat formation in mice.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Trichothiodystrophy involves brittle hair due to low sulfur amino acids, not a transport defect.

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

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

FOXC1 boosts SFRP1 in hair loss, suggesting new treatments.

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

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

EBF1 controls hair type and length.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

Lack of Fgf21 slows hair growth by affecting gene interactions.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.