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Gorab deficiency speeds up skin aging by disrupting protein regulation and reducing collagen.

Root hairs help Arabidopsis plants absorb more phosphorus when it's scarce.

A specific gene variant may increase the risk of developing Alopecia Areata.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

The model accurately predicts skin conditions in Korean women using genetic information, aiding personalized skincare.

Identified genes linked to male-pattern baldness may help develop new treatments.

Certain genetic markers can help predict wool production in U.S. sheep.

Researchers found a non-functional sheep keratin gene due to mutations.

FGF13 gene changes cause excessive hair growth in a rare condition.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

A new gene causes hairlessness and skin cysts in rats.

Genetic factors can predict male pattern baldness risk.

Some women with PCOS have rare genetic variants linked to the condition.

Hairless gene not strongly linked to baldness.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Reduced matriptase activity causes skin and hair issues in both humans and mice.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Scientists found genes linked to hair length in Brangus cattle that could help breed heat-tolerant cattle.

Different species use the same genes for tooth regeneration.

A new gene mutation causes a rare type of hair loss.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

Parental socioeconomic status doesn't improve dietary habits or reduce disease severity in children with sickle cell disease.

Certain genes in fat tissue affect weight loss in women with PCOS.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

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

A new DSG4 gene mutation causes hair defects in a young girl.