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New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

Topical putrescine and spermine increased DNA synthesis in hairless mouse skin.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Neutrophils quickly respond to skin injury.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Antizyme slows skin tumor growth by reducing cell growth in mice.

Mutations in keratin genes cause skin, hair, and nail disorders, with future treatments possible.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

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

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

Genetically modified rats help reveal how vitamin D affects bone and skin health.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Loss of Dnmt3a and Dnmt3b leads to more aggressive skin tumors, but blocking PPAR-γ can reduce this effect.

SLC24A5 shows a clear selective sweep, but no link to UV radiation intensity.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.