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Long-term use of Risperidone may be linked to a serious skin condition in bipolar patients, affecting their overall well-being.

The antibody 005-C04 blocks prolactin receptors, causing reversible infertility, impaired lactation, and hair regrowth in female mice.

New probes were created to effectively measure specific enzymes involved in fat metabolism, which could help develop new drugs.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

A genetic variant in the KRT25 gene causes tightly curled hair.

Solid Lipid Particle technology makes retinol more stable, effective, and gentle on the skin.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

A new treatment using a special gel with miR-665 reduces inflammation and helps hair regrow in alopecia areata.

LIPH mutations cause woolly hair in some Chinese people.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.

Ritlecitinib effectively improves hair regrowth and physician satisfaction in severe alopecia areata over time.

A new patch can deliver stable antibodies over time for potential HIV treatment.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

Certain histamine receptors (H2R, H3R, H4R) have unique roles in treating skin diseases, with H2R helping with chronic urticaria and other conditions, H3R providing pain relief and allergy benefits, and H4R reducing inflammation and itchiness.

The treatment cleared psoriasis in some patients but caused side effects in most.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

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

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

rPanglaoDB helps study rare cell types by merging RNA data, confirming fibrocytes' role in healing.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Rose stem cell nanoparticles improve skin quality by boosting collagen, aiding cell movement, reducing melanin, and lowering inflammation.

Early skin biopsy is crucial for diagnosing Conradi-Hünermann-Happle syndrome.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.