The document's conclusion cannot be provided because the document is not accessible or understandable.
July 2004 in “Hair transplant forum international” The document's conclusion cannot be provided because the document is not available for parsing.
February 2026 in “European Urology” February 2006 in “Inpharma Weekly”
17 citations
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October 2006 in “Molecular and Cellular Endocrinology” The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.
3 citations
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December 2021 in “Frontiers in endocrinology” A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.
August 2020 in “OPAL (Open@LaTrobe) (La Trobe University)”
June 2017 in “Journal of The American Academy of Dermatology” The new treatment was safe and may effectively treat male pattern hair loss.
June 2023 in “British Journal of Dermatology” The prototype for analyzing skin aging works technically and clinically.
May 2010 in “Europe PMC (PubMed Central)” Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.
July 2022 in “British Journal of Dermatology” September 2024 in “Journal of the American Academy of Dermatology” July 2026 in “Pediatric Allergy and Immunology”
January 2007 in “대한피부과학회지” The document's conclusion can't be summarized because the text is not in English and the document content is not provided.
July 2025 in “Journal of Investigative Dermatology”
September 2022 in “Piretc” The document's conclusion cannot be provided because the document is not accessible or understandable.
October 2024 in “Frontiers in Oncology” A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.
January 2004 in “Drug Development and Industrial Pharmacy” GI197111X is best dissolved in Capmul MCM for trials.
September 2019 in “The journal of investigative dermatology/Journal of investigative dermatology” A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.
July 1991 in “Endocrinology” The document contains an error.
10 citations
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July 2001 in “Hair transplant forum international” The document's conclusion cannot be provided because the document is not readable or understandable.
1 citations
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December 2022 in “BMC Genomics” The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.
67 citations
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February 2009 in “Journal of Dermatology” March 2009 in “European Urology Supplements”
2 citations
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July 2011 in “AFRICAN JOURNAL OF BIOTECHNOLOGY” Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.
March 2024 in “Research Square (Research Square)” The TT genotype of a specific SNP in sheep is linked to better wool quality.
3 citations
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July 2022 in “Brain and Behavior” The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.
4 citations
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August 2013 in “Chinese Medical Journal” A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.
December 2018 in “Dermatologic Surgery”
January 2015 in “DOAJ (DOAJ: Directory of Open Access Journals)” A simple, precise method was created for estimating Tamsulosin and Finasteride in medicine using common lab solvents, showing good precision and stability.