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

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

Scientists successfully created mouse hair proteins in the lab, which are stable and similar to natural hair.

Finasteride crystals are held together by hydrogen bonds and weak interactions, forming synthon pseudopolymorphs.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

A specific gene mutation causes sparse, brittle hair in a family.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

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

Peptide hydrogels are promising for drug delivery and tissue repair in medicine.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

FAKΔe4 helps cells sense and respond to different stiffness levels in their environment.

Trichocytic cytokeratin expression starts earlier in whiskers than in body hair during rat embryo development.

The 5050 MHA42MCS45 hydrogel blend is suitable for repairing load-bearing soft tissues.

The new GelMet hydrogel can effectively support skin cell growth for tissue engineering.

Newly designed proteins can effectively degrade specific proteins in cells, offering a promising alternative for targeted protein degradation.

Accurate protein modeling can help develop new treatments for prostate cancer and other diseases.

A new mutation in the HR gene causes hair loss in a specific family.

Newly designed proteins can effectively degrade specific proteins in cells, offering a potential new therapy method.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

Hair follicles form hard α-keratin filaments in four steps, showing structural differences.

Human mitochondrial DNA polymerase makes very few errors, crucial for preventing degenerative diseases.

The method effectively analyzes human hair proteins, especially nonfilamentous ones.

New mutations in the DSG4 gene cause a rare hair condition.

Human hair keratin has a 40% α-helix structure that changes to a random coil in 8 M urea.