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Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

Merkel cell carcinoma is most likely to recur within two years of diagnosis, and factors like immune suppression, being over 75, and male sex increase this risk.

Switch hair can indicate magnesium and copper levels in beef cows.

A new method accurately measures molecular movement without complex modeling.

A compound named ZCZ90 can increase muscle spindle firing, potentially helping treat muscle spasms and hypertension.

A new method was developed to accurately detect and measure 47 different drug ingredients in various products.

Dermoscopy may not show hookworms clearly, and comparing it with tissue studies could improve diagnosis accuracy for skin conditions caused by parasites.

Chemical treatments can change the scale heights of wool and cashmere fibers, affecting their identification.

Mitochondrial genes help predict breast cancer outcomes and spread.

MX1 and AR genes are linked to milder COVID-19, while TMPRSS2 increases severe risk, especially in women.

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

The document couldn't be read, so there's no conclusion to summarize.

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

A new perming method is less damaging to hair and works as well as traditional methods.

Combining MSM with MAP significantly promotes hair growth.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

Pigmented rings with central clearing help diagnose melasma more accurately.

FM dyes effectively stain Merkel cells for long-term observation.

Monilethrix is a rare genetic hair disorder with no cure, but low-dose oral minoxidil may help.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Children with marasmus have more resting hair follicles and thinner, less pigmented hair, showing long-term malnutrition.

Specific keratin gene mutations can cause monilethrix.

MRL/MpJ mice's skin wounds heal with scars, unlike their ear wounds which can regenerate.

Injecting α-MSH made mice's hair turn black.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.