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Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Severe alopecia areata patients have a low chance of spontaneous hair regrowth.

Patients with severe alopecia areata felt better and less anxious or depressed when treated with baricitinib compared to placebo.

Thyroid-related genes are active in skin cells and may affect autoimmune conditions.

PROTO1 and PROTO2 protect against hearing damage.

Mycophenolate mofetil may improve lupus nephritis remission more than cyclophosphamide but with uncertain safety.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

The review concluded that reporting on PRP therapy is often incomplete, leading to uncertainty about its effectiveness.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

PCOS causes infertility mainly due to hormonal imbalances, insulin resistance, and chronic inflammation.

A new strain of bacteria from the human skin can help prevent hair loss.

People with Alopecia Areata have more herpes simplex infections but similar rates of cancer, blood clots, and heart disease compared to those without it.

Melatonin improved secondary hair growth in goats but didn't affect primary hair density or litter size.

Younger people are at a higher risk for Fibrosing Alopecia in a Pattern Distribution than previously thought, with common symptoms and possible involvement of mast cells in its development.

Long-lasting symptoms like fatigue and breathlessness can persist after COVID-19, requiring ongoing medical follow-up.

PAD is common but often missed, needing lifestyle changes and medication for better outcomes.

No single treatment is clearly effective for central serous chorioretinopathy.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Early recognition and treatment of Peripheral Arterial Disease is crucial to improve survival and health outcomes.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

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

Scientists successfully made a human growth factor in a plant, which could help with hair growth and bone development.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Intralesional triamcinolone injections can effectively stop frontal fibrosing alopecia with minimal side effects.

Cells with active Wnt signaling are less likely to turn into cancer when exposed to a cancer-causing gene.

Higher hair luminosity and shine mean higher perceived transparency.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.