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The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

The study found that Tourette Syndrome may be linked to certain immune system processes and synaptic signaling.

The agouti gene may help understand and treat obesity.

Certain plasma proteins are linked to prostate cancer risk and could help in early detection and treatment.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

Hairlessness in mammals is caused by combined changes in genes and regulatory regions.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

Seven new genetic risk areas for prostate cancer were found.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

The study identified key genes and pathways linked to hair disorders, aiding precision medicine.

Certain genetic variants increase the risk of aggressive prostate cancer.

A new mouse mutation causes skin and hair issues, influenced by another gene.

Modified β-catenin can cause different effects in mouse skin cells, leading to cysts or tumors depending on the cell type.

New genetic factors linked to acne risk were discovered, highlighting the role of certain pathways and genes.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

Gene regulatory regions evolve faster than protein coding regions, allowing new gene relationships without changing transcription factors.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Certain genetic changes in the STX17 and KRT82 genes contribute to hair loss in alopecia areata.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Trichotillomania may have a genetic link to psychiatric disorders.

MCHR2 gene duplications may be linked to alopecia areata.

Allergies and atopic conditions may increase the risk of developing alopecia areata.

Atg5 can promote tumors when autophagy is deficient but suppresses them under normal conditions.