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Children with pituitary dwarfism have higher zinc and copper, lower manganese, and similar iron levels in hair compared to normal children.

Laminin-511 is involved in psoriasis development and can be regulated by cannabinoid receptor type 1.

Mutations in the HOXC13 gene cause hair and nail development issues.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

The BHBS is a valid tool to study cultural norms and breast cancer risk in Black women.

Hirsutism is too much hair growth in women like the pattern in men, often caused by high male hormones, and can be treated with hormone control and hair removal methods.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Hyperbaric oxygen therapy may improve hair and scalp health.

Blocking the enzyme 11β-HSD1 might help treat obesity and metabolic issues.

Hair follicle cells resist turning into skin cells.

IL-18 levels are higher in hidradenitis suppurativa patients and may indicate disease severity.

Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

The assay effectively detects hormonal activity of certain chemicals.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Individuals with this condition often develop male traits and identities at puberty despite being raised as females.

A mutation in the human hairless gene causes alopecia universalis.

EZH2 is essential for hair growth and skin cell development.

Overexpression of the HE4 gene in mice causes eye inflammation and cloudiness.

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Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

The clinic-based hair fall count method is accurate and reliable.

Glucocorticoids and thyroid hormones together are essential for fetal fat development.

Proper tissue repair in adult skin requires specific histone hypomethylation.

Laminin α5 is essential for skin communication and health.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

UHP-sCESr is as effective as HESr for treating BPH symptoms.

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

JAK inhibitors can be safely used for alopecia areata in patients with latent hepatitis B or stable tuberculosis with proper monitoring.