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Liver disease is linked to hair loss, especially in women and those with unhealthy lifestyles.

Specific mutations in a receptor cause facial abnormalities and hair loss.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Pyruvate Kinase M2 helps hair grow by linking energy production and a key hair growth pathway.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Oxidative stress is important in causing alopecia areata.

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

ALKBH5 helps wounds heal faster by stabilizing PELI2 mRNA.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

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

TYK2 inhibition may help treat alopecia areata by promoting hair growth and reducing immune response.

OR2AT4 helps reduce aging and cell damage in human skin cells.

Specific keratin gene mutations can cause monilethrix.

The tested hair dye ingredients do not form harmful oxidized metabolites in the liver.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Allopregnanolone is needed for certain brain processing issues caused by D1 dopamine receptor activation.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

The enzyme system in hair follicles is similar to the liver's and is inhibited by certain substances.

Altering SSAT affects fat metabolism and body fat in mice.

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

A molecule called α-ketobutyrate was found to extend lifespan and improve aging-related symptoms in worms and mice by activating certain cellular pathways and may help develop anti-aging treatments for humans.

DHEA boosts bone cell growth and differentiation in elderly stem cells.