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A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

β-thymosin in invertebrates is more complex and diverse than in vertebrates.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

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

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

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

Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.

Desmosomes are crucial for skin and heart development, and JNK may help regulate them.

Trichothiodystrophy involves brittle hair due to low sulfur amino acids, not a transport defect.

Key genes and RNAs related to hair growth in sheep were identified, aiding future breeding improvements.

Tjalma Syndrome is a rare condition in people with lupus, causing fluid buildup and high CA-125 levels, but not due to tumors.

CTCF protein is essential for skin and hair follicle development in mice.

TG5 helps maintain hair follicle health, while TG3 aids in hair shaft development.

Trichohyalin is a protein in hair follicles that helps form hair filaments.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Tenascin-C and tenascin-W help control stem cell movement and growth in whisker follicles.

Certain proteins are significantly increased in the skin of people with hidradenitis suppurativa.

The 14-3-3σ gene is essential for preventing hair loss.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

β‐thymosins, especially thymosin β4, help in heart protection, wound healing, and hair growth by stabilizing actin in cells.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

Bendamustine combined with tucidinostat may effectively treat adult T-cell leukemia.

A woman's mature cystic teratoma caused her virilization by producing testosterone.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.