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About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

The assay effectively identifies compounds that affect immune cell activation.

Giant axonal neuropathy changes the structure of keratin in human hair.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Gore-Tex is effective for severe congenital ptosis, with the open approach better for no lid crease and the closed approach better for a preserved crease.

Certain interactions help prepare the androgen receptor for pairing and activation, which is important for its role in development and disease.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

Blocking EGFR in mice causes hair loss and skin changes.

LGD1069 effectively prevents breast tumors in mice without toxicity.

Fadrozole and Finasteride change frog sex ratios and cause intersex animals with altered gene expressions.

Translation levels actively determine keratinocyte cell fate.

The new technique for repositioning lower eyelid fat with a midface lift is easier, faster, and has better results with fewer complications.

The condition might be caused by genetic changes after birth.

A specific gene mutation causes a severe skin disorder in a family.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

Overexpression of LRIG3 in skin causes hair loss.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Creating evidence-based guidelines for gender incongruence is difficult due to the personalized nature of transgender medicine.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

The agouti gene may help understand and treat obesity.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.

Thioglycolic acid and L-cysteine change hair structure differently during perms, affecting hair strength and curling efficiency.

Overexpression of certain genes can shorten hair by disrupting the hair-growth cycle.

The Itpr3 gene causes a specific hair pattern in mice.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.