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High-Performance Liquid Chromatographic Determination of the Enantiomers of the Benzoquinolinone LY 191704, a Human Type 1 5α-Reductase Inhibitor, in Plasma

research High-performance liquid chromatographic determination of the enantiomers of the benzoquinolinone LY 191704, a human type 1 5α-reductase inhibitor, in plasma

1 citations , March 1997 in “Journal of Chromatography B: Biomedical Sciences and Applications”

Researchers developed a method to measure different forms of a drug that could help treat prostate issues and hair loss, and found how these forms behave in animals.

research Prostaglandin E ₂ Receptor 2 Modulates Macrophage Activity for Cardiac Repair

29 citations , September 2018 in “Journal of the American Heart Association”

EP 2 receptor is essential for heart repair by helping macrophages work properly.

PRO-C22 - A Novel Serological Biomarker of Tissue Damage Is Associated with Disease Severity, Disease Activity, and Systemic Inflammation in Patients with Hidradenitis Suppurativa

research 51826 PRO-C22 - A Novel Serological Biomarker of Tissue Damage is Associated with Disease Severity, Disease Activity, and Systemic Inflammation in Patients with Hidradenitis Suppurativa

September 2024 in “Journal of the American Academy of Dermatology”

PRO-C22 can help diagnose and monitor the severity of hidradenitis suppurativa.

research Allopregnanolone is required for prepulse inhibition deficits induced by D1 dopamine receptor activation

12 citations , June 2019 in “Psychoneuroendocrinology”

Allopregnanolone is needed for certain brain processing issues caused by D1 dopamine receptor activation.

research Nucleocytoplasmic Communication in Progeria

April 2014 in “Libra”

Defective nuclear transport may cause gene expression changes in Progeria.

research Curly : a new hair defect mutation in the SELH/bc mouse strain

January 2009

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

research Advances in the genetic understanding of hypohidrotic ectodermal dysplasia

1 citations , November 2017 in “Expert opinion on orphan drugs”

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

research A Group of Type I Keratin Genes on Human Chromosome 17: Characterization and Expression

38 citations , February 1988 in “Molecular and Cellular Biology”

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

research Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes

6 citations , July 2024 in “Heliyon”

Steroid 5α-reductase evolved from protists and diversified in eukaryotes, with specific roles in mammals and plants.

research Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis

3 citations , March 2019 in “European Journal of Dermatology”

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

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