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Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

Msx2 and Foxn1 are both crucial for hair growth and health.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

Researchers found a genetic region that influences the number of coat layers in dogs.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

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

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

Certain gene variations are linked to better memory in healthy Chinese women.

Understanding hair follicle development can help treat hair loss, skin regeneration, and certain skin cancers.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

Increasing research diversity is key for better understanding and treating Parkinson's Disease.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Treat pattern hair loss with finasteride and topical minoxidil.

Most people in the surveyed area experience hair loss, but they are not aware of the role of diet, iron, hormones, genetics, and possibly water quality in causing it.

Certain astrocytes can protect the brain and improve recovery after a stroke, and a hair loss drug might reduce cancer spread.