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Genetic differences affect breast cancer treatment success with tamoxifen in South African patients.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

Androgen self-administration might be controlled by membrane receptors, not nuclear ones.

The dual-wavelength laser system effectively reduces EFFC symptoms with minimal side effects.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Injecting recipient splenocytes into donors' thymus can prevent graft-versus-host disease.

MultiKano accurately identifies cell types in complex data better than existing methods.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

A new peptide, DualPep-ALO, may help hair growth by reducing inflammation and boosting growth factors.

VDDR I and II are genetic disorders affecting vitamin D use, causing rickets, with VDDR I treatable by vitamin D supplements and VDDR II needing high doses and calcium.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Using both hands to place grafts makes the process quicker and less painful.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

Mice lacking steroid 5α-reductase 2 show less aggression and better impulse control.

Dermal EZH2 controls skin cell development and hair growth in mice.

γδ T cells adapt uniquely to different tissues in mice.

A specific gene variation in goats is linked to better growth traits.

A new gene mutation causes insulin resistance in a girl and her mother.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

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A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

The dfRootChip revealed how Arabidopsis roots adapt and grow in uneven conditions.

Four transcription factors can convert mouse cells into hair cell-like cells, aiding hearing loss research and treatment.