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The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

Microspheric skin organoids can be used for drug testing, identifying Minoxidil as a Wnt pathway activator.

Cow milk sugars increase fat production and inflammation in skin oil cells.

Managing malignant ureteral obstruction is challenging and requires personalized treatment to protect kidney function and patient health.

MLO proteins are crucial for root hair growth by regulating calcium and ROS levels.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Mouse and human skin development share similar fibroblast timelines.

A compound named ZCZ90 can increase muscle spindle firing, potentially helping treat muscle spasms and hypertension.

Spiny mice have resilient, large mitochondria that help them regenerate tissue.

Light-based bioelectronic devices improve health monitoring and disease treatment.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

LncRNAs play a crucial role in muscle regulation and could help develop treatments for Duchenne muscular dystrophy.

A new method can almost perfectly distinguish adenomyosis from similar conditions using blood tests.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

Low-level laser therapy, now called photobiomodulation, is recognized for its broad medical applications and scientific backing.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Perhexiline can effectively target ovarian cancer cells left after treatment.

Combined light therapy improves eye health and quality of life for those with meibomian gland dysfunction.

CD34⁺ cells help heal damaged limbs by promoting blood vessel growth.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Enobosarm significantly increased muscle mass and improved physical function in elderly men and postmenopausal women without serious side effects.

Microneedles are becoming essential tools in medicine for sensing, drug delivery, and communication.

Suppressing ODC activity reduces tumor growth in hair follicles.

A woman with a rare form of multiple myeloma had a headache and a skull mass, which led to her diagnosis after tests and a biopsy.