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A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Exosomes from umbilical cord stem cells help heal complex perianal fistulas in rats.

We need safe, affordable drugs to fight coronaviruses effectively.

Using protein degradation to fight cancer drug resistance shows promise but needs more precise targeting and fewer side effects.

Advancements in wound healing aim to improve personalized treatments and enhance healing outcomes.

Jasmonic acid and its derivatives play important roles in plant health and have potential uses in medicine and agriculture.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

Bendamustine combined with tucidinostat may effectively treat adult T-cell leukemia.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

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

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

MED1 affects skin wound healing differently in young and old mice.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

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

Jasmonic acid helps plants grow, defend against threats, and survive stressful conditions like drought and salt.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

Methyl jasmonate boosts tanshinone production in Salvia miltiorrhiza callus cultures.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

Myotonic dystrophy may be classified as a segmental progeroid disorder.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.