11 citations
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January 2000 in “The Journal of Steroid Biochemistry and Molecular Biology” LY320236 is a strong blocker of two enzymes that change testosterone into dihydrotestosterone and might help treat conditions related to male hormones.
1 citations
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November 2023 in “SKIN The Journal of Cutaneous Medicine”
September 1998 in “Hair transplant forum international” The document's content cannot be summarized because it is not accessible or understandable.
January 2005 in “Hair transplant forum international” The document's conclusion cannot be provided because the document is not readable or understandable.
September 2008 in “Hair transplant forum international” August 2023 in “Zenodo (CERN European Organization for Nuclear Research)” March 2010 in “European Urology Supplements” July 2024 in “Reactions Weekly”
January 2024 in “Hair transplant forum international” I'm sorry, but I can't provide a summary without the content of the document.
September 2023 in “Hair transplant forum international” I'm sorry, but I can't provide a summary without the content of the document.
July 2023 in “Hair transplant forum international” I'm sorry, but I can't provide a summary without the content of the document.
36 citations
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July 2014 in “Neuromuscular Disorders” A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.
2 citations
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October 1990 in “The Lancet” Some people have a genetic variation that makes them less effective at breaking down drugs.
January 2025 in “Dermatology Reports” Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.
11 citations
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April 2019 in “Bioscience Reports” Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.
July 2022 in “British Journal of Dermatology” 143 citations
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May 2002 in “PubMed” LGD1069 effectively prevents breast tumors in mice without toxicity.
June 2018 in “International Review of Intellectual Property and Competition Law”
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September 2022 The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.
February 2025 in “Archives animal breeding/Archiv für Tierzucht” Certain gene combinations improve cashmere quality and production in Liaoning goats.
November 2000 in “Hair transplant forum international” The document's conclusion cannot be provided because the content is not accessible.
July 1998 in “Hair transplant forum international” The document's content could not be processed or understood.
May 2022 in “Hair transplant forum international” The document could not be processed or understood.
September 2020 in “Oxford University Press eBooks” Unable to provide a summary as the provided text does not contain enough information.
July 2024 in “Journal of Investigative Dermatology” DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.
10 citations
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January 2003 in “Dermatology” The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.
July 2022 in “Zenodo (CERN European Organization for Nuclear Research)” May 2025 in “Reactions Weekly”
March 2006 in “Hair transplant forum international” The document's conclusion cannot be summarized because the content is not understandable.
3 citations
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August 2010 in “Letters in Drug Design & Discovery”