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A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Lack of TrkC receptor delays hair follicle development.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

Poncirin is a promising inhibitor of Janus Kinase 3, potentially better than tofacitinib.

ATP-sensitive potassium channels are important for hair growth.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

Increased Stat3 activity reduces hair follicle stem cells and boosts other stem/progenitor cells.

A protein called MPZL3 in mitochondria slows down hair growth and could be a target for treating hair growth disorders.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Keratin 17 is crucial for cell growth in wound healing by aiding protein synthesis.

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

Stat3 activation increases hair follicle progenitors but reduces bulge region stem cells.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Advancements in skin treatment and wound healing include promising gene therapy, 3D skin models, and potential new therapies.

Mouse keratin 6 genes evolved independently from human ones and are regulated differently.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

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

Rapamycin treatment helps with mitochondrial disease by reducing PKC levels.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

TGM3 is important for skin and hair structure and may help diagnose cancer.

A new keratin gene was found in mice, explaining hair growth.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

MPZL3 protein helps keep sebaceous gland size and cell growth in check.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.