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Optimizing the structure of a specific compound greatly improved its effectiveness and precision for treating diabetic complications.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

Farudodstat may effectively treat alopecia areata without harmful side effects.

N-oxides are important in medicine for improving drug properties and targeting.

Vitamin D receptor binds similarly to natural and synthetic ligands, affecting gene regulation.

Using polyethylenimine-DNA to deliver the hTERT gene can stimulate hair growth and may be useful in treating hair loss, but there could be potential cancer risks.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

A boronic acid copolymer quickly forms cell clusters, useful for tissue and tumor modeling.

A new method allows for controlled, long-lasting delivery of retinoic acid through the skin with less inflammation.

RpoS helps Borrelia burgdorferi survive in hosts and adapt to different environments.

A new, less toxic and more efficient method to create the anti-baldness compound RU58841 was developed in 2014.

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

Retinoic acid and DMSO improve gene delivery to mouse skin for potential hair and skin disease treatment.

The new hair-dyeing shampoo is safe, colors hair evenly, and strengthens it.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Platelet-rich plasma, microneedling with minoxidil, and topical finasteride are promising treatments for hair loss.

The exosome injections were from stem cells and plants, not umbilical cords.

RNA-based treatments show promise for managing Hutchinson-Gilford Progeria Syndrome.

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

Polymer JR400 sticks to hair but washes off with detergent.

Two siblings have a rare hair condition caused by a new genetic variant.

A substance called poly(I:C) increases a protein called carbonic anhydrase II in skin cells, which might help with skin defense and healing.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

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

2-deoxy D-glucose does not help with hair regrowth in alopecia areata.

The DPCP/HPβCD complex improves solubility and anti-inflammatory effects for alopecia areata treatment.