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Microneedle patches with alpha-arbutin and resveratrol can effectively reduce skin pigmentation without irritation.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

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

This new method makes checking for female infertility less painful, less invasive, and doesn't use radiation.

The drug combination was safe and showed promise in treating advanced tumors.

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Four antibodies were developed to help study hair follicle cell differentiation.

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CSLD1 suppresses rice root hair growth with NH4+ and regulates AMT1;2 expression.

Tofacitinib effectively treated a woman's severe symptoms from a rare autoimmune condition.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

FoxN1 overexpression in young mice harms immune cell and skin development.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

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Cats with abnormal hair had DSG4 gene changes causing hair problems.

Human amniotic membrane helps heal skin wounds faster and with less scarring.

Microneedle patches with different pore sizes can effectively deliver drugs and trigger strong immune responses.

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The protein DDX6 helps keep skin cells renewing properly by controlling the production of certain other proteins and breaking down those that cause cells to mature too quickly.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

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

Viral reactivation is rare at the time of DRESS diagnosis in the U.S.

New treatments for immune disorders caused by FOXN1 deficiency are promising.