November 2022 in “Journal of Investigative Dermatology” Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.
1 citations
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September 2021 in “Frontiers in genetics” A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.
July 2020 in “Hair transplant forum international” The document's content could not be processed.
March 1999 in “Hair transplant forum international” The document's content could not be processed.
January 1999 in “Hair transplant forum international” The document's content could not be processed.
January 2003 in “Dermatology” 
July 2022 in “The journal of investigative dermatology/Journal of investigative dermatology” A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.
21 citations
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April 2014 in “PLoS ONE” A rare gene variant causes hair and nail issues in a family.
June 2023 in “British Journal of Dermatology” A person with Werner syndrome was initially thought to just have female pattern hair loss.
January 1997 in “Hair transplant forum international” The document's conclusion cannot be provided because the content is not available for analysis.
January 2026 in “Nature Reviews Urology” 
November 2016 in “Hair transplant forum international” The document's content couldn't be processed to provide a conclusion.
September 2018 in “Translational Andrology and Urology” 
May 2019 in “Hair transplant forum international” The document's content could not be processed or understood.
90 citations
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January 1989 in “PubMed” Metabolic processes and key genes like FGF5, FGFR1, and RRAS significantly affect hair follicle growth in Inner Mongolian Cashmere goats.
![Activity of 17β-(N-Alkyl/Arylformamido) and 17β-[(N-Alkyl/Aryl) Alkyl/Arylamido]-4-Methyl-4-Aza-5α-Androstan-3-Ones as 5α-Reductase Inhibitors in the Hamster Flank Organ and Ear](/images/research/861159f1-7bd4-420c-a16b-4829458efe68/small/15592.jpg)
10 citations
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August 1998 in “Journal of Investigative Dermatology” The compounds tested could potentially treat hair loss and alopecia.
3 citations
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June 2017 in “Reproductive biomedicine online” A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.
August 2023 in “Zenodo (CERN European Organization for Nuclear Research)” 1 citations
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January 2023 in “Frontiers in genetics” Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.
April 2010 in “Dermatology Times” 2 citations
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January 2022 in “The Application of Clinical Genetics” A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.
4 citations
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December 2013 in “The Journal of Dermatology” A new mutation in the K6b gene caused a girl's late-appearing nail condition.
January 2005 in “Hair transplant forum international” The document's conclusion cannot be provided because the document is not readable or understandable.
April 2023 in “Journal of Investigative Dermatology” AL136131.3 slows hair growth by affecting energy processes in hair loss.
March 2026 in “American Journal of Clinical Dermatology” 
August 2016 in “Organic Process Research & Development” Authors retracted paper due to errors in data and mislabeling.
November 2016 in “Hair transplant forum international” The document's conclusion cannot be provided because the document cannot be parsed.
July 2010 in “Hair transplant forum international” The document's conclusion cannot be provided because the document cannot be parsed.
March 2010 in “Hair transplant forum international” The document's conclusion cannot be provided because the document cannot be parsed.