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TRPA1 and TRPV1 channels don't affect mechanotransduction in rat sinus hair follicles.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

TCDD reduces EGF receptor activity and causes various developmental changes in animals.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

Human keratinocytes do not naturally respond to androgens.

BRG1 is essential for skin cells to move and heal wounds properly.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

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

Two enzymes regulate androgen receptor activity, affecting treatments for androgen insufficiency and benign prostatic hyperplasia.

TLR2 helps control hair growth and regeneration, and its reduction with age or obesity can impair hair growth.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

Activating TLR3 may help produce retinoic acid, important for tissue regeneration.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

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

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

Blocking CXCR4 may help treat hidradenitis suppurativa.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Krox20 is important for maintaining stem cells in the skin and affects hair growth and color.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

A truncated protein linked to breast cancer may change cell adhesion.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

High glucocorticoids cause pancreatic malfunction and malabsorption, reversible with enzyme supplements.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

A specific gene mutation causes a severe skin disorder in a family.