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Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Crossbreeding certain European cattle breeds may cause hair and physical issues in cattle.

Recombinant human epidermal growth factor is versatile, effective, and safe for long-term skin and mucosal treatments.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

ILK is essential for skin development, pigmentation, and healing.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

CD61 is important for mouse tooth cell growth and works through Lgr5.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

STAT3 signaling is important for healthy skin and hair follicles, and its disruption can lead to skin conditions like atopic dermatitis.

Dermal EZH2 controls skin cell development and hair growth in mice.

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

Charnoly bodies could be a marker for cell damage, and certain nutrients and proteins might prevent them, potentially helping with brain diseases and cancer.

The Itpr3 gene causes a specific hair pattern in mice.

Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Improving knowledge and practices in animal fibre production is crucial to meet market demands and potentially revive natural fibres.

The research reveals how early embryonic mouse skin develops from simple to complex structures, identifying various cell types and their roles in this process.

Vav2 and Vav3 proteins help control skin stem cell numbers and activity in both healthy and cancerous cells.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Animal models, especially mice, are essential for advancing hair loss research and treatment.