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Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Frontal Fibrosing Alopecia is a poorly understood condition that is hard to treat and causes distressing hair loss.

Case-only trees and random forests improve predictions of treatment effects in clinical trials.

Regulating certain sex hormones may help delay facial aging.

Obesity worsens PCOS symptoms, and PCOS may lead to more weight gain; managing both requires a holistic approach that includes mental health.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Blocking the CXCR3 receptor reduces T cell accumulation in the skin and prevents hair loss in mice.

A gene variation is linked to hair thickness in Asians.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Single Blimp1+ cells can create functional sebaceous gland organoids in the lab.

Hair follicle culture helps develop new treatments for hair loss.

People with alopecia areata have higher levels of a heart disease marker than those without hair loss.

ULBP3 could be a marker for diagnosing alopecia areata incognita and may be linked to its cause and development.

The document concludes that diagnosing and treating hair loss is complex and requires understanding its psychological effects and underlying causes, while also calling for more research and new treatments.

A patient with total hair loss developed vitiligo after using a treatment called DCP.

Animal models, especially mice, are essential for advancing hair loss research and treatment.

Higher social status is linked to earlier diagnosis and better treatment results for Frontal Fibrosing Alopecia in women.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

Found new possible treatments for hair loss.

Half of people with Alopecia Areata may see hair regrowth within a year without treatment, but recovery is unpredictable.

Ruxolitinib effectively regrows hair in most patients with severe hair loss.

A patient with Alopecia Areata had complete hair regrowth after using the drug baricitinib.

Restoring hair bulb immune privilege is crucial for managing alopecia areata.

TCDD speeds up skin barrier formation by increasing certain gene expressions.