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

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

P63 is a marker for epidermal stem cells in rats.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Phosphatide distribution in mouse skin remains consistent in both normal and cancerous growths.

SQSTM1 gene issues may increase the risk of alopecia areata.

NCBP3, SDHA, and PTPRA are the best genes for accurate goat skin research.

Grasp protein helps maintain skin health after UVB exposure.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

Tudor-SN is important for immune cells, and polyamines can promote hair growth.

TGF-beta 1 and IGF-II mRNA have specific patterns in pig subcutaneous tissue, affecting fat and muscle development.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

IL-19 and IL-24 help cells respond to DNA damage and could be targeted for cancer and age-related disease treatments.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

P311 helps skin stem cells become myofibroblast-like cells, aiding wound healing.

Recent selection on immune response genes was identified across seven ethnicities.

Phospholipids help plant proteins move by regulating receptor interactions.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Human prostate cells produce more WISP1/CCN4 when there's not enough oxygen.

Protein kinase C epsilon may increase skin cancer risk by affecting nearby cells.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

p63 and p73 regulate the vitamin D receptor, affecting cancer cell behavior and vitamin D sensitivity.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.