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Overexpression of SSAT in mice causes hair loss, liver damage, and sensitivity to polyamine analogues.

The ferret had a malignant apocrine gland tumor and did not survive surgery.

miR-486 may help prevent hair loss in alopecia areata.

Certain tyrosine kinases may regulate hair growth and could help develop hair loss treatments.

Genetic marker rs12558842 strongly linked to male hair loss.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

CD117 and platelet-derived growth factor receptor α may play a role in alopecia areata.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Two specific genes are more active during hair growth in mice.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Cathepsin L deficiency causes hair and skin issues in mice.

Mice with autoimmune hair loss showed signs of heart problems.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Alefacept does not effectively treat severe alopecia areata.

Epimorphin helps shape and develop epithelial cells, like those in hair follicles.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Very-long-chain acyl-CoA synthetases and fatty acid transport proteins play key roles in fatty acid metabolism and lipid processing in different tissues.

Pemigatinib may be effective for treating ZMYM2::FGFR1 fusion-positive leukemia.

Increasing isoleucine intake improved skin and health issues in an infant with maple syrup urine disease.

BST2 protein and certain T cells increase in early alopecia areata.