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LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

Feather patterns are influenced by enhancers and chromatin looping, and the structure of protein complexes important for hair growth has been detailed.

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

Fine wool sheep have more genes for wool quality, while coarse wool sheep have more for skin and muscle traits.

A 3-month stay in space causes skin thinning, disrupts hair growth, and changes muscle-related genes in mice.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

TNC+ fibroblasts play a key role in skin inflammation by interacting with T cells.

Understanding gene expression in hair follicles can reveal insights into hair growth and disorders.

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

EGFR helps control how hair grows and forms without needing p53 protein.

Staphylococcus epidermidis A/C strains are more antibiotic-resistant and infection-adapted, while B strains thrive in hair follicles.

The zinc finger protein 3 in Arabidopsis thaliana reduces plant growth and root hair development.

Get3d protein helps maintain photosynthesis in plants and photosynthetic bacteria.

A mother's PPARγ is crucial for preventing harmful milk that can cause inflammation and growth problems in babies.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

The conclusion is that we need more effective hair loss treatments than the current ones, and these could include new drugs, gene and stem cell therapy, hormones, and scalp cooling, but they all need thorough safety testing.

Stem cell differentiation is crucial for skin barrier maintenance and its disruption can lead to skin diseases.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

The study found that hair fragility in Pili annulati may be caused by cavities and damage within the hair shafts.

Understanding and manipulating epigenetic changes can potentially lead to human organ regeneration therapies, but more research is needed to improve these methods and minimize risks.

Two mouse mutations cause similar hair loss despite different skin changes.

A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.

The review concludes that innovations in regenerative medicine, tissue engineering, and developmental biology are essential for effective tissue repair and organ transplants.

Human hair keratin genes are similar to mouse genes and are specifically expressed in hair follicles.

The PP2A-B55α protein is essential for brain and skin development in embryos.

Minoxidil improves blood flow and vessel flexibility, potentially helping with vascular stiffness.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

The study found that immune responses disrupt hair growth cycles, causing hair loss in alopecia areata.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.