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Wrinkled skin in Xiang pigs is linked to gene changes related to oxidative stress and the extracellular matrix.

Premature hair graying in the face may be influenced by genetics and environment.

Whn is essential for hair growth, and its malfunction causes hair loss.

The angora mouse mutation causes long hair and hair defects due to a gene deletion.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

The study found that certain microRNAs are higher in the cells and lower in the fluid of women with a specific type of polycystic ovary syndrome, and one microRNA could potentially help diagnose the condition.

A genetic change in the FGF5 gene affects hair growth in cashmere goats.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

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

Keratin 17 is important for hair and nail structure and affects pachyonychia congenita symptoms.

A genetic variant in goats is linked to cashmere growth.

Increased ornithine decarboxylase makes normally tumor-resistant mice more sensitive to tumors.

Tight junctions help control skin shedding and may be targets for treating certain skin conditions.

Hereditary factors cause hair loss in mice by affecting skin and hair follicle structure.

The CUBIC protocol allows detailed 3D visualization of proteins in mouse skin biopsies.

Mesenchymal stem cells from laser-assisted liposuction are as effective and safe as those from conventional liposuction for cell therapy.

The timing of when the gene Bmal1 is active affects aging and survival, with its absence during development, not adulthood, leading to premature aging.

Vimentin and transthyretin proteins are linked to black coat color in sheep.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

IL16 gene variations may affect the risk of alopecia areata in Koreans.

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

Scientists turned rat thymus cells into stem cells that can help repair skin and hair.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Key genes can rewire networks, changing skin appendage types.

Certain microRNAs in the fluid around eggs are linked to Polycystic Ovary Syndrome and may help diagnose it.

T-cells in alopecia areata scalp show abnormal regulation, leading to less inflammation.