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Loss of Msx2 function causes eye development issues similar to Peters anomaly.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

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

Current methods can't fully recreate skin and its features, and more research is needed for clinical use.

Certain natural and synthetic compounds may help treat inflammatory skin diseases by targeting a specific signaling pathway.

Autophagy helps keep skin healthy and may improve treatments for skin diseases.

The scalp has more diverse bacteria, while hair has more bacteria and unique types.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

Human dental pulp stem cell-conditioned medium, especially from hypoxic conditions, may help treat chemotherapy-induced hair loss and does not increase cancer risk.

miRNA-based therapies show promise for treating skin diseases, including hair loss, in animals.

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Scientists have improved 3D models of human skin for research and medical uses, but still face challenges in perfectly replicating real skin.

A fragment of human type XVII collagen shows great potential for skin health and wound healing.

Different stem cells are key for hair growth and health, and understanding their regulation could help treat hair loss.

Human skin xenografting could improve our understanding of skin development, renewal, and healing.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

Vitamin A is important for healthy skin and hair, influencing hair growth and skin healing, but UV light reduces its levels.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

NF-κB is crucial for zebrafish heart repair, affecting heart cell growth and repair processes.

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

PlacMA hydrogels from human placenta are versatile and useful for cell culture and tissue engineering.

Eclipta prostrata has many traditional uses and health benefits, but more research is needed to understand how it works and ensure it's safe.

Single Blimp1+ cells can create functional sebaceous gland organoids in the lab.

Hair changes can indicate systemic diseases or medication effects.

Activin activation in skin cells speeds up wound healing without affecting scar quality.