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Ultrasound measurement of the ovarian stroma to total area ratio is not a reliable single predictor of high male hormone levels in Thai women with PCOS, but works better when combined with clinical signs.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

SRD5A2 methylation in blood can predict how well someone will respond to finasteride treatment.

A rare gene variant causes hair and nail issues in a family.

Reduced matriptase activity causes skin and hair issues in both humans and mice.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

Wnt10b promotes hair growth, while SFRP2 inhibits it in Wanxi Angora rabbits.

The RHD4 gene is crucial for consistent root hair growth in Arabidopsis thaliana.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Skin disorders in Sari differ from other parts of Iran, with acne and hair loss being most common.

Ishige sinicola extract helps bone-building cells grow and mature, which could aid in treating osteoporosis.

LLPS is crucial for RALF signaling, aiding plant growth and stress resilience.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

Strontium ranelate helps cartilage growth by blocking a specific cell pathway.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

RXR-alpha is strongly expressed in both normal and psoriatic skin and may help in skin cell differentiation and hair growth.

A rare case of isolated trichothiodystrophy was identified, marked by brittle hair with low sulfur content.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Scientists restored fertility in male mice lacking a key fertility gene by using a modified gene.

Human stem cells can turn into functional eye cells that might help treat retinal diseases.

A Korean baby with nevus sebaceus syndrome was found to have a KRAS gene mutation.

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Trimethoprim-sulfamethoxazole can cause aseptic meningitis, especially in people with certain health conditions.

Trichothiodystrophy is a condition with brittle hair and various physical and mental issues due to low sulfur in proteins.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

KLHL24-mutant stem cells help understand skin and heart disease.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.