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BI 2536 had limited effectiveness against several advanced cancers and caused significant side effects.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

miR-877-3p can improve cashmere quality by regulating hair growth in goats.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Long noncoding RNAs help regulate hair follicle density in rabbits.

Researchers found two new genetic variants linked to Alzheimer's disease.

KY19382 helps regrow hair and create new hair follicles.

A humanized IL-2 fusion protein boosts T regulatory cells and helps control hair loss in Alopecia Areata.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Susan Lee Lindquist was a pioneering biologist who made significant contributions to understanding protein folding and its role in disease.

Long non-coding RNAs play a role in hair growth stages of Hetian sheep, affecting wool quality.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Changes in certain RNA and protein levels may contribute to alopecia areata and could be treatment targets.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

LONRF1 is important for oxidative damage response and tissue remodeling during wound healing.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

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

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

FOXN1 duplication can cause excessive hair growth.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.