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Identical p53 gene mutations in different cancers suggest the need for careful treatment.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Longer CAG repeats in gene linked to more severe hair loss in females.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Topical minoxidil can cause excessive hair growth in children, so use it carefully.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

A gene called BMAL1 plays a role in controlling hair growth.

MC4R gene variants not linked to female hair loss.

Certain gene variations are linked to better memory in healthy Chinese women.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

Finasteride affects SRD5A2 gene pattern, possibly causing lasting side effects.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

A genetic marker linked to a type of hair loss was found in most patients studied.

Certain gene variations might be linked to severe acne in women but not in men.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.