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The new patch made of cell matrix and a polymer improves wound healing and supports blood vessel growth.

Diagnosing Sertoli-Leydig cell tumors is challenging due to their unusual symptoms and can occur at any age.

The LTF gene may help predict and manage nonspecific orbital inflammation.

KLHL24-mutant stem cells help understand skin and heart disease.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

A new method quickly creates controllable cell clusters for tissue engineering and drug testing.

ZmSPL10, ZmSPL14, and ZmSPL26 genes are essential for forming maize structures needed for pollen capture and kernel production.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

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

ETS2 is crucial in squamous cell carcinoma development and could be a therapeutic target.

SM04554 may increase hair growth as a topical treatment for androgenetic alopecia.

The SOSTDC1 gene is crucial for determining sheep wool type.

Ca 45 mainly enters rat skin and eye through biosynthesis and may be adsorbed in cartilage and glands.

3D models and organoids improve liposarcoma research and therapy development.

SLHA can be hard to diagnose and needs teamwork between specialists.

A new laser technique can precisely remove specific cell types in living animals without harming nearby cells.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

LSD1 is crucial for regenerating hair cells in zebrafish.

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

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

The K14 promoter is more active in skin cells than the K5 promoter.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

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

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

A man with X-ALD improved after treatment, highlighting the need to consider X-ALD in similar patients and test their relatives.