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A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Scientists found new, better-working inhibitors for a hormone-related enzyme.

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

The new drug delivery system effectively targets lung cancer cells.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

The study found genetic diversity in coat color dilution among Czech pointers in Slovakia.

The study created a model to help design new inhibitors for steroidal 5α-reductase enzymes.

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

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Adding cerium(III) chloride to Grignard reagents improves the making of compounds that could treat prostate issues and hair loss.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

RCS-01 cell therapy is safe and improves skin gene expression.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

A new mutation in mice causes crooked whiskers and messy hair.

A new patch can deliver stable antibodies over time for potential HIV treatment.

R-spondins and their receptors help increase bone growth and may be used to treat bone loss diseases.

Accurate diagnosis of RDEB-mitis in older adults is crucial for proper management without immunosuppressants.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

PX-12 may help treat psoriasis by blocking inflammation and cell death.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

A 589 nm laser increases IL-2 and IFN-y gene expression in human T-cells.

The scraggly mutation causes hair loss and skin defects in mice.

ASLNC168501 may help restore hair growth in androgenetic alopecia by improving hair follicle stem cell function.

circRNA-1926 helps goat stem cells turn into hair follicles by affecting miR-148a/b-3p and CDK19.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.