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RADA16-I can effectively deliver and release mangiferin, improving its solubility and bioavailability.

Chemical modifications can alter hair's stability and flexibility, with hydrophobic interactions helping maintain structure in humid conditions.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Glycol chitosan hydrogels enable quick, safe 3D cell spheroid formation for various applications.

Keratin proteins in epithelial cells are dynamic and crucial for cell processes and disease understanding.

Keratinocyte adhesion problems can cause skin and hair disorders.

Keratin K80 is an ancient protein found in various tissues, important for cell structure and tissue differentiation.

The family has a unique form of ectodermal dysplasia similar to Clouston syndrome but with different hair and skin symptoms.

Hydrogel surface properties affect mouse embryoid body differentiation.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Gremlin proteins help regulate hair growth by balancing signals in hair follicles.

Farudodstat may effectively treat alopecia areata without harming hair follicles.

Researchers found a new mutation causing total hair loss from birth.

Mitochondria change shape to meet energy needs during cell movement.

Scientists created 3D hair-like structures that could help study hair growth and test treatments.

A protein-based hydrogel helps heal diabetic wounds and repair nerves.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

Researchers identified promising inhibitors for the BRD4 protein, including finasteride and amentoflavone.

Biomimetic dermal papilla spheres can help regenerate hair to some extent.

Mouse keratin 6 genes evolved independently from human ones and are regulated differently.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

The protein structures in the hair and tendon were preserved, but their molecular arrangements changed.

Researchers created a new mouse model for studying scleroderma.

New mutations in the hairless gene may cause hair loss and affect bone development.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

A specific gene mutation causes a severe skin disorder in a family.

A specific protein in chicken embryos links early skin layers to feather development.

Encapsulating hair follicle cells in a special gel boosts their activity.