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

Alpha-MSH affects mitochondrial function, and MC1R mutations may increase skin aging.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

A gene mutation in mice causes severe skin disorder similar to a human condition.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

scMC effectively separates biological signals from technical noise in single-cell genomics data.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

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

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

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

MIR135b affects wound healing by targeting genes, and PDRN may help heal wounds by altering this pathway.

A girl had rickets due to a gene mutation affecting vitamin D response.

Muscarinic acetylcholine receptors in skin cells help regulate and promote hair growth.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

Mcl-1 can activate Wnt signaling in skin cells, promoting growth and possibly cancer.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

The Celsr1 gene is crucial for normal hair patterning in mice.

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

A new mouse mutation causes skin and hair defects due to a gene change.

MC-1R in skin cells may influence inflammation and collagen production.