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Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

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

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

A new genetic mutation was found causing hair and eye issues in a boy.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

Electrostatic interactions mainly stabilize the binding of peptides to hair keratin.

A specific DNA duplication in Polish chickens affects feather shape by altering gene expression.

Dermal EZH2 controls skin cell growth and differentiation in mice.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

Hair protein differences help identify species and individuals in forensic science.

Certain skin proteins can form anchoring structures without the protein AMACO.

A new method using solid-state circular dichroism anisotropy can distinguish similar chiral compounds better than traditional techniques.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Cross-linked proteins help maintain the structure of hair, feathers, and hagfish teeth.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

The hydrogel is versatile and easy to make.

Alkylation of human hair keratin allows for adjustable drug release rates in hydrogels for medical use.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

New hydrogel sensors can be quickly made and customized for wearable devices.

A protein called desmoglein 3 is important for keeping hair follicle stem cells inactive and helps in their regeneration.

The technique showed that human hair has two main parts, with 68% being rigid and the rest flexible, and water swelling affects its structure.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

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