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RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

UC.145 may be a new biomarker for predicting gastric cancer.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Parry–Romberg Syndrome can involve the brain even without obvious symptoms, and a new diagnostic framework is suggested for early detection.

RNA from horse hair follicles can track circadian rhythms non-invasively.

BBR-SA nanomedicine is a safe and effective treatment for breast cancer.

The conclusion is that differentiating wound types in RDEB patients is important for clinical trials and understanding the disease.

Changing YBX1 protein activity affects skin stem cell function and aging.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

Capsaicin cream quickly relieved itching in two patients with brachioradial pruritus.

A new method accurately measures molecular movement without complex modeling.

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.

OR2AT4 helps reduce aging and cell damage in human skin cells.

cDermo-1 causes dense skin, feathers, and scales in chickens.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

Bacterial cellulose is a promising material for biomedical uses but needs improvements in antimicrobial properties and degradation rate.

RORs may influence cashmere growth cycles.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

A new mutation in mice causes crooked whiskers and messy hair.

The regenerative medicine industry saw business growth with new partnerships, clinical trials, and financial investments.

Proton minibeam radiotherapy shows promise for sparing healthy tissue in cancer treatment but needs further research and technological development.

A 50 mg non-loading dose of ritlecitinib is safe for adults and adolescents.

A new gene mutation causes insulin resistance in a girl and her mother.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

Early diagnosis and proper treatment improve outcomes for methylmalonic acidemia.

Stereotactic Radiosurgery is an effective non-invasive treatment for cerebral AVM, with successful outcomes and minimal side effects.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.