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A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

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Scientists created a detailed map of gene activity in different parts of human hair follicles.

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Key genes can rewire networks, changing skin appendage types.

Exosomes from special stem cells help treat ulcerative colitis by reducing inflammation and stress.

Nonmelanoma skin cancers have higher levels of certain osteopontin variants than normal skin.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

The method effectively showed that the two exemestane preparations are bioequivalent.

Ectoin helps prevent cortisone-induced skin problems and supports skin health.

Injectable exosomal micro RNAs may help regrow hair.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

Nexin 1 may help control hair growth.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

Radiation therapy in breast cancer patients changes gene expression related to DNA damage, fibroblast growth, and hair follicle development, which could help improve treatment for radiation-induced fibrosis.

Oncology specialists are disappointed by the discontinuation of the effective lymphoma treatment Bexxar.

The research helps in creating genetically modified animals to study hair growth.

Hoxd gene regulation in mammals and birds is robust despite differences in DNA sequences, due to 3D chromatin structures.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Hair follicle samples effectively show how well the drug MK-0752 targets and engages with the Notch pathway.

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

Specific keratin gene mutations can cause monilethrix.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

Hex gene plays a crucial role in starting feather development in chick embryos.