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The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

Genetic differences may influence male pattern hair loss in Russians.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

Genetic analysis is crucial for diagnosing and managing cerebral arteriopathy.

Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.

Researchers found a specific T cell receptor linked to severe drug reactions like Stevens-Johnson syndrome when patients take carbamazepine.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

A new method, iSiMPRe, effectively identifies key protein regions in cancer genes, highlighting potential drug targets.

PBX1 reduces aging and cell death in stem cells by boosting SIRT1 and lowering PARP1.

Activating TSPO helps protect the retina from damage caused by high eye pressure in glaucoma.

A specific gene mutation causes severe skin and nail issues and hair loss.

Ca²⁺-mediated protein citrullination controls cell growth in the CNS and may help treat brain tumors.

Intranasal delivery of gene therapy shows promise for treating ischemic stroke.

The study found genetic variations in sheep that affect traits like milk production, growth, and health.

CCL5 is important for the hair growth potential of human dermal papilla cells.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

SRD5A2 methylation in blood can predict how well someone will respond to finasteride treatment.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

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

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.