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The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

Losing both ERBB2 and ERBB3 receptors in mice causes significant skin problems and inflammation.

Manipulating 5α-reductase type 2 can affect liver fat production and glucocorticoid effects.

The Bethesda system is effective for identifying thyroid cancer but has low sensitivity.

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

Sex steroids influence skin appendage function and neoplasm development, with changes in AR and ERalpha in certain gland neoplasms.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

LRIG1 is linked to better survival in Merkel cell carcinoma.

Ber‐EP4 marks cells related to the secondary hair germ in hair follicles.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

The ZIP13 variant is linked to abnormal hair quality.

Biopsy is crucial for accurately diagnosing EPDS to avoid mistaking it for SCC.

Personalized treatment based on detailed tumor analysis successfully managed and reduced the patient's aggressive hair follicle cancer.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

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

SQSTM1 is linked to increased risk of alopecia areata.

Rhupus is a complex syndrome that is hard to diagnose due to unclear clinical criteria.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

The Enterobacter isolate AMS1-S8 is effective for removing selenium from wastewater.

LGR6+ stem cells may improve bone healing.

Methylation of the 5-AR2 gene may cause resistance to Finasteride in BPH patients.

Higher EULAR/ACR scores in SLE patients predict more organ damage.

Mutations in specific genes cause different types of ectodermal dysplasias.

The HCR gene contributes to psoriasis risk.

Rushton's hyaline bodies form from hair keratin and blood substances.

ERK activation spreads between cells in mouse skin, linked to cell division and influenced by TPA and EGF receptors.