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

TAZ boosts fat cell formation in goat stem cells by activating a specific signaling pathway.

MPA increases cancer spread by boosting Eph A2 activity.

Congenital Adrenal Hyperplasia is mainly caused by enzyme deficiencies, leading to varying symptoms like hormone imbalances and physical changes.

Stem cell therapy from umbilical cords may help treat atopic dermatitis.

The new AI software predicts melanoma outcomes more accurately than traditional methods.

The HATMSC1 cell line from fat tissue can produce helpful factors for regenerative and immune therapies.

Two brothers from Bangladesh were diagnosed with X-linked adrenoleukodystrophy, showing neurological and adrenal symptoms.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

E-cadherin is important for cell movement in electric fields, and the new tracking method works well.

Forensic DNA phenotyping can help generate new leads in cold cases but faces accuracy, legal, and acceptance challenges.

MXD@CP could be a promising new topical treatment for hair loss.

A quick and simple method was created to identify minoxidil in hair-growth products using micellar electrokinetic capillary chromatography.

Detecting early breast arterial calcifications can help assess cardiovascular disease risk.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

Computational methods help design drugs targeting prostate cancer proteins.

AMN can cause bladder problems due to nerve damage.

MSC-CM improved aged skin in mice.

Two microRNAs in stem cell exosomes help treat hair loss by targeting a specific signaling pathway.

StemMACS media is better for growing therapeutic stem cells than PowerStem media.

Immunotherapy with pembrolizumab significantly reduced cancer in a young woman with adrenocortical carcinoma.

The "exposure–crossover design" helps assess individual changes in risk after events like car crashes.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Adrenocortical carcinoma is a rare, aggressive adrenal gland cancer with a poor outlook.

Upadacitinib can cause hypersensitivity that worsens ulcerative colitis symptoms.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

The model can effectively help diagnose meibomian gland dysfunction automatically.