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Researchers found four genes that could help diagnose severe alopecia areata early.

Certain genetic changes in the KAP22-1 gene are linked to better wool quality in Egyptian sheep.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Thymosin β4 helps increase hair growth in Cashmere goats.

Sonic hedgehog proteins may help grow hair.

Beta-caryophyllene, found in essential oils, helps wounds heal better in multiple ways.

Green tea extract helps prevent cell death and supports cell survival in hair cells exposed to a chemotherapy drug.

Hair ages due to various factors and treatments like minoxidil and finasteride can help, but more research and better public awareness are needed.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

The article concludes that studying how skin forms is key to understanding skin diseases and improving regenerative medicine.

Corticosteroids are the most common treatment for alopecia areata, but many patients need better options.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Different amounts of daylight affect cashmere growth in goats by changing the activity of certain genes and molecules.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

Tiny particles from 3D-grown skin cells speed up wound healing by promoting blood vessel growth.

AGA, a common hair loss, is caused by genetics, hormones, age, and environmental factors.

Goat skin changes with the seasons due to genes affected by daylight and hormones.

Forensic medicine is crucial for justice and needs continuous innovation and technology integration.

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

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.

PF-05314882 selectively activates androgen receptors without much effect on prostate and may help in prostate cancer treatment and hair loss prevention.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

Dorper sheep's wool shedding is linked to specific genes and pathways, which may help understand human hair growth.

Surface-modified nanostructured lipid carriers can improve hair growth treatments.