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Ketoconazole increases finasteride's effectiveness and lifespan in the body.

PRP growth factor concentrations vary, no significant hair growth difference found.

Night shift work disrupts the body's natural clock genes.

Type 2 diabetes does not change how metformin works in obese pregnant women, so dosage adjustments are not needed.

Finasteride's solubility improves with native y-CDs, enhancing hair loss treatment and reducing side effects.

Targeting FGFR-1 with antisense oligonucleotides may help treat baldness by increasing hair follicle activity.

Centipedegrass extract may promote hair growth by activating certain cell pathways.

Swallowing a lot of minoxidil, a hair growth liquid, can cause severe and long-lasting low blood pressure.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

Hair loss and excessive growth treated with various options, including new laser technology.

Hair antiretroviral concentration is affected by hair type, segment position, housing, drug use, sexual behavior, kidney function, and genetics.

Genetic marker rs12558842 strongly linked to male hair loss.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Mutations in the hairless gene cause a rare form of permanent hair loss.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Mutation in hairless gene may increase hair loss risk.

Mutation in hairless gene may increase hair loss risk.

MCHR2 gene duplications may be linked to alopecia areata.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

Recent selection on immune response genes was identified across seven ethnicities.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

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