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PTHRP agonists can stimulate hair growth, especially in damaged follicles, while antagonists may initially increase growth but ultimately inhibit it.

TDM10842, a thyroid hormone receptor activator, was found to effectively promote hair growth in mice.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Researchers found a non-functional sheep keratin gene due to mutations.

Early diagnosis and treatment are crucial to prevent permanent hair loss from TNFα inhibitors in scalp psoriasis.

People from iodine-deficient areas are more likely to develop hypothyroidism when treated for multi-drug resistant tuberculosis.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

Thymic stromal lymphopoietin (TSLP) promotes hair growth, especially after skin injury.

5% topical minoxidil improves hair density and quality in monilethrix patients.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Increased ornithine decarboxylase makes normally tumor-resistant mice more sensitive to tumors.

[6]-Gingerdiol 3-monoacetate shows promise for treating T. whipplei infections.

Progerin affects cell shape but not hair or skin in mice.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

Calprotectin starves Pseudomonas aeruginosa of essential metals, affecting its growth and resistance.

Two siblings were diagnosed with Trichothiodystrophy, identified by brittle hair and low sulfur content.

SPT6 prevents excessive skin inflammation by blocking a feedback loop.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

A girl with citrullinemia developed pili torti, suggesting a link between the hair condition and the metabolic disorder.

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

CXCR2 in skin cells promotes tumor growth.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

The ACE1 gene variant doesn't affect long-COVID symptoms.

Blocking a specific receptor slows down hair loss in mice.