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Nanoparticles improve drug delivery through the skin but more research is needed on their long-term effects and skin penetration challenges.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

Hox proteins help maintain keratinocyte identity by regulating miRNA expression.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

Skin stem cells maintain and repair the outer layer of skin, with some types being essential for healing wounds.

George Ernest Rogers was a notable scientist who made important discoveries about hair and wool proteins.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

The study provides insights into hair growth mechanisms in yaks.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

Lymphatic vessels are essential for health and can be targeted to treat various diseases.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

Certain DNA regions in alpacas are linked to fiber diameter.

Dermal Papilla Cells grown in 3D and with stem cells better mimic natural hair growth conditions than cells grown in 2D.

Shift work disrupts the body's natural clock, leading to health problems.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

The HPV type 11 region activates hair-specific gene expression in mice.

Hair analysis can show nutritional status and environmental exposure, with phosphorus being very stable in hair and differences found based on gender and conditions like depression and autism.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Some hair protein genes evolved early and were adapted for use in hair follicles.

Male pattern baldness involves hormone-related hair thinning, shorter hair, and inflammation.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.