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The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

Peptide nanoparticles can effectively deliver CRISPR-Cas9 to target KRAS mutations in cancer.

Deleting podoplanin in mice promotes hair growth by enhancing cell migration.

SQSTM1 gene issues may increase the risk of alopecia areata.

Targeting ACE2 and TMPRSS2 may help prevent or treat COVID-19 in cancer patients.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Four-amino acid part makes enzyme sensitive to finasteride.

A new mouse mutation causes skin and hair issues, influenced by another gene.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

A 12-year-old boy with twenty nail dystrophy, a condition affecting all nails, was treated conservatively due to its self-limiting nature and good prognosis.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

The research showed that Vitamin D and its receptor are important for healthy bones and normal hair and skin in rats.

RET mutation is important in familial medullary thyroid carcinoma, and BRAF mutation in papillary thyroid carcinoma is linked to more aggressive cancer and higher death rates.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

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

The study concludes that the EDA2R gene is activated by p53 during chemotherapy but is not necessary for chemotherapy-induced hair loss.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

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

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.