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

Certain signals are important for reducing specific chemical markers on hair follicle stem cells during rest periods, which is necessary for healthy hair growth.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

Mutations in certain receptors can cause diseases and offer new treatment options.

Cashmere and milk goats have different hair growth cycles and gene expressions, which could help improve wool production.

Skin aging is caused by stem cell damage and can potentially be delayed with treatments like antioxidants and stem cell therapy.

The spiny mouse is a unique menstruating rodent that can help us understand menstruation and reproductive disorders.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

Understanding how epigenetic regulation affects stem cells is key to cancer insights and new treatments.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

Hair in mammals likely evolved from glandular structures, not scales.

Keratoacanthoma comes from hair follicle cells.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Hormones affect skin aging and fat distribution, and treatments can help, but only minoxidil is proven for female hair loss.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Hair loss in autoimmune blistering skin diseases varies and may regrow with disease control.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Stem cell therapies show promise for treating various diseases but face challenges in clinical use and require better monitoring techniques.

The document concludes that stem cell inactivity is actively controlled and important for tissue repair and balance.

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

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

Keratin genes change gradually during skin cell development and should be used carefully as biomarkers.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.