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Overexpressing thrombospondin-1 in mice skin prevents UVB-induced skin damage.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

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

GPC1 is important for hair growth by helping blood vessels form around hair follicles.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

Four new FGF5 gene variants cause long hair in dogs.

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

S100A6 protein is linked to disease progression, especially in cancers.

HPV8 E6 gene causes growth of certain skin stem cells.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

CD25+ CD4+ Tregs and certain plasma proteins are linked to hair loss.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

The KRTAP19-5 gene affects wool curvature in Chinese Tan sheep, with Variant B reducing curvature.

TGFBR1 slows down cell growth in fine-wool sheep hair follicles.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.