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Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Systemic sclerosis skin shows varied gene patterns, suggesting potential for personalized treatment.

Recognizing minor skin lesions can help identify serious cancer syndromes.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

CE-PTG is a better method for analyzing hair growth in androgenetic alopecia.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

TOF-SIMS improved chemical mapping in cells, confirming gunshot residue, tracking anti-tumor drugs, and identifying molecules in mosquitoes and wounds.

Tudor-SN is important for immune cells, and polyamines can promote hair growth.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

The research found that a protein called PPARg is important for the formation and healing of sebaceous glands, which can regenerate independently from hair follicles.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Targeting CXXC5 and GSK-3β may help treat male pattern baldness.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

FTY720 helps transplanted fat survive better by reducing immune rejection and improving blood vessel growth.

Stress hormone corticosterone blocks a growth factor to slow down hair stem cell activity and hair growth.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

Integrin alphavbeta6 is important for wound healing and hair growth, and blocking it may improve these processes.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

Claudin 6 is crucial for normal skin and hair development.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.