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Rats can't grow new hair follicles after skin wounds, unlike mice, due to differences in gene expression and response to WNT signaling.

Understanding hair biology is key to developing better treatments for hair and scalp issues.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

Apoptosis is essential for human skin development and forming a functional epidermis.

Chemotherapy often causes hair loss, which usually grows back within 3 to 6 months, but there's no effective treatment to prevent it.

Current treatments for hair loss from chemotherapy are limited, but new methods are being researched.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

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

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Keratins are important for skin cell health and their problems can cause diseases.

Scientists made skin stem cells from other human cells with over 97% efficiency, which could help treat skin conditions.

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

Circadian rhythms are crucial for stem cell function and tissue repair, and understanding them may improve aging and regeneration treatments.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Hormones and neuroendocrine factors control hair growth and color, and more research could lead to new hair treatment options.

Targeting the HEDGEHOG-GLI1 pathway could help treat keloids.

Significant progress was made in understanding PXE, but effective treatments are still needed.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

The vitamin D receptor helps regulate skin and hair health independently of its usual vitamin D ligand.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

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.

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

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Current research explores hair growth drugs, while future research aims for personalized treatments.