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A substance called poly(I:C) increases a protein called carbonic anhydrase II in skin cells, which might help with skin defense and healing.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

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

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

A new type of nerve cell involved in itch perception was discovered.

Low IRES/Cap translation is linked to higher stem cell potential.

MCHR2 gene duplications may be linked to alopecia areata.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Ribonucleotide excision repair is crucial to prevent skin cancer.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Chinese fine-wool sheep have genetic variations linked to traits like milk and health, with some genes under strong selection.

Vitamin D receptor gene variations are not linked to alopecia areata.

miRNAs in the Dlk1-Gtl2 region may improve lamb fur quality.

New compounds effective against SARS-CoV-2 variants were identified using a rapid testing method with human lung cells.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

EDA2R gene linked to hair loss.

EGFR inhibitors can cause unusual localized hair growth.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

scINSIGHT helps understand single-cell gene expression better than current methods.

Men taking 5-alpha reductase inhibitors for prostate issues may be less likely to experience severe COVID-19, but it doesn't prevent ICU admission or death.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

The study suggests that higher levels of SIRT1 and SIRT2 may improve overall cell health and aging processes.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

ZD1839 can cause skin issues like acne and hair changes.