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Memory T cells in the skin balance staying put and moving into the blood, clustering around hair follicles, and increasing in number after infection.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

Mitochondriopathy may cause eyelash loss.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

H. pylori infection is not linked to PCOS or infertility.

A CCS patient with severe complications was successfully treated using combined therapies.

Melanocyte stem cells can become melanoma, resembling human melanoma.

A woman with a skin disorder was found to have hepatitis C, which may be linked, and was safely treated with methotrexate.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

A patient with pemphigus vulgaris improved significantly after treatment for an additional viral skin infection.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Changes in genes FGA, VWF, and ACTG1 may contribute to pemphigus vulgaris.

HPV8 causes hair follicle stem cells to grow, leading to skin lesions.

Early screening and HPV vaccination reduce cervical cancer risk.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

αMSH may help regulate immune responses in hair follicles and its disruption could lead to hair loss.

Thymoma-associated multiorgan autoimmunity can cause liver damage and affects multiple organs, with limited treatment options and a generally poor prognosis.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

Melanocyte stem cells from non-affected skin in vitiligo patients can become functional melanocytes for potential therapy.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

Total glucosides of paeony may help treat alopecia areata by reducing inflammation and hair loss.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

M-CSF-stimulated myeloid cells can cause alopecia areata in mice.

Oncogenic melanocyte stem cells can develop into melanoma similar to human cases.