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The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

Endoplasmic reticulum stress plays a key role in developing atherosclerosis.

The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.

NDRG1 protein helps infantile hemangioma, a common infant tumor, to grow, and its mismanagement by FOXO1 protein plays a big role in causing the tumor.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Electron Beam Tomography (EBT) is a useful additional test to stress testing for detecting heart disease.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Local injections of nanosized rhEPO can speed up skin healing and improve quality after deep second-degree burns.

The IRE gene is important for normal root hair growth in Arabidopsis plants.

Platelet-rich plasma can improve erectile function in older individuals by reducing prostate enlargement.

Armadillo Repeat Only proteins are essential for proper plant growth and response by regulating calcium channels.

Rodent spiny hair traits are due to genetic factors other than the Edar gene.

Endocrine-disrupting chemicals cause irreversible harm to children's development, increasing disease risk.

Dopaminergic neurons in the gut have diverse subtypes with different neurotransmitter contents.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

RNase L suppresses regeneration in mammals.

Changes in NRF2 levels may contribute to hair loss in Egyptian men.

Vepdegestrant may become the first FDA-approved PROTAC degrader, marking a new era in drug development.

The EDAR gene greatly affects hair thickness in Asian populations.

RDW is a useful, cost-effective tool for diagnosing and monitoring various diseases.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Understanding how EDC genes are regulated can help develop better drugs for skin diseases.

Normal skin cell renewal doesn't need RAR signaling, but vitamin A-related skin thickening does.

A feedback loop between LRH and RSL4 controls root hair growth in Arabidopsis.

A vitamin D receptor mutation causes rickets and affects immune responses.