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ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

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

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

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

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

UVA exposure worsens hair loss by activating a specific cell pathway.

Human keratinocytes do not naturally respond to androgens.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

TGase 3 helps build hair structure by forming strong bonds between proteins.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

The treatment was not recommended due to limited effectiveness and significant side effects.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

Prostaglandin D2 increases testosterone production in skin cells through a process involving reactive oxygen species, and antioxidants may help treat hair loss.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

DHT stops hair regrowth in mice, similar to human hair loss.

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