13 citations
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November 2009 in “Journal of Dermatological Science” A gene mutation causes woolly hair in a Syrian patient.
81 citations
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December 2009 in “Journal of Dermatological Science” Fat tissue stem cells may help increase hair growth.
December 2024 in “Dermatology”
SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.
October 2012 in “Sax's Dangerous Properties of Industrial Materials” July 2024 in “Journal of Investigative Dermatology” DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.
March 2023 in “Oxford University Press eBooks” 39 citations
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September 2018 in “American Journal of Medical Genetics Part A” A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.
November 2022 in “Journal of the Endocrine Society” A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.
109 citations
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February 2018 in “CB/Current biology” ERULUS controls root hair growth by regulating cell wall composition and pectin activity.
January 2023 in “Indian dermatology online journal” A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.
June 2018 in “The Journal of Sexual Medicine” Finasteride helps female-pattern hair loss.
August 2016 in “Journal of Investigative Dermatology”
21 citations
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April 1982 in “Genetics Research” Mice with the naked gene have missing or abnormal hair cells.
11 citations
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March 2020 in “American Journal of Medical Genetics Part A” A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.
September 1997 in “International Society of Hair Restoration Surgery” January 2025 in “Case Reports in Genetics” A rare gene variant causes sexual development issues in siblings, needing personalized treatment.
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November 2018 in “American Journal of Medical Genetics Part A” ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.
1 citations
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January 2016 in “Australasian Journal of Dermatology” A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.
October 2002 in “Dermatologic Surgery” research 22
December 2023 in “Psychiatry Neurology and Medical Psychology”
March 2023 in “Oxford University Press eBooks” The document's conclusion cannot be determined from the provided text.
11 citations
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July 2014 in “Gene” The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.
November 1995 in “Hair transplant forum international” The document cannot be understood or processed.
The naked mutation in mice causes hair loss and helps identify keratin genes.
8 citations
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July 2015 in “International Journal of Dermatology” A new DSG4 gene mutation causes hair defects in a young girl.
5 citations
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January 2011 in “Archives de Pédiatrie” A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.
4 citations
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March 2007 in “Hair transplant forum international” The document's conclusion cannot be provided as the content is not available.
April 2018 in “Journal of Investigative Dermatology”