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Activating cannabinoid receptor 1 reduces certain keratin levels, potentially aiding psoriasis treatment.

Touch dome keratinocytes in adult skin have traits of different skin cell types.

High ODC and low K1 and K10 may indicate early skin tumors in mice.

Notch signaling is crucial for specifying niche cells in Drosophila testis.

KY19382 helps regrow hair and create new hair follicles.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

Keratins are important for skin cell health and their problems can cause diseases.

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

Keratin 19 forms less stable and shorter filaments than keratin 14, giving unique traits to certain skin cells.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

Acidic keratin genes are on CFA9 and basic keratin genes are on CFA27 in dogs.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Keratin 2e shows a unique pattern in developing fetal skin, different from other keratins.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Hair follicles prevent NK cell attacks to avoid hair loss.

Mycophenolate mofetil improved skin condition in a man with nephrogenic fibrosing dermopathy.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

Removing the VDR gene in skin cells reduces their growth and affects hair-related genes.

Natural killer and CD8+ T cells play a key role in hair loss in androgenetic alopecia.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Activating Kras in mouse skin causes excess skin and hair loss.

AGD1's PH domain is essential for its role in root hair growth and polarity.

Mice without active or present vitamin D receptors maintain normal blood sugar control and islet gene expression when calcium levels are normal.

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

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requires high doses of calcium and vitamin D for management.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

A protein called ectodysplasin-A2 increases a hair growth inhibitor in balding cells, which could be a target for hair loss treatment.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.