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Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Melanocyte precursors in human fetal skin follow a specific migration pattern and some remain in the skin's deeper layers.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Changes in KRT17 gene activity linked to wool production in Angora rabbits.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

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.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

miR-31 regulates hair growth by controlling gene expression in hair follicles.

Hair follicle stem cells might help treat traumatic brain injury.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

MicroRNAs are important for skin health and could be targets for new skin disorder treatments.

Corneous beta-proteins evolved uniquely in reptiles and birds, forming scales, claws, beaks, and feathers.

OsPHR2 gene causes excessive phosphate in rice shoots, affecting plant growth and root development.

Sons of mothers with polycystic ovary syndrome (PCOS) have a higher risk of obesity and insulin resistance, possibly due to certain genes and factors passed down from their mothers.

MicroRNAs can reprogram cells into stem cells faster and more efficiently than traditional methods.

Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

The document concludes that hair biology is complex and there are still unanswered questions about hair loss and follicle changes.

Inflammation around hair follicles leads to hair loss, and treatments should focus on reducing this inflammation and other factors for effectiveness.