January 2022 in “Figshare” I cannot summarize the document because it cannot be parsed.
April 2016 in “The Journal of Sexual Medicine”
8 citations
,
October 2019 in “Immunological investigations” The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.
July 2025 in “Journal of Investigative Dermatology”
August 2016 in “Journal of Investigative Dermatology” Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.
28 citations
,
March 2010 in “British Journal of Dermatology” Genetic marker rs12558842 strongly linked to male hair loss.
1 citations
,
September 2023 in “Acta dermato-venereologica” Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.
June 2018 in “International Review of Intellectual Property and Competition Law” 7 citations
,
August 1996 in “The Journal of Clinical Endocrinology and Metabolism”
July 2008 in “Hair transplant forum international” The document cannot be understood or processed.
September 2023 in “Journal of The American Academy of Dermatology” The document's conclusion cannot be provided because the content is not available.
A specific gene change in APCDD1 increases the risk of hair loss.
3 citations
,
January 2018 in “Postępy Dermatologii i Alergologii” Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.
14 citations
,
August 2018 in “Journal of Pharmaceutical and Biomedical Analysis” December 2023 in “International Journal of Dermatology”
40 citations
,
January 2017 in “Intestinal Research” Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.
June 2023 in “Zenodo (CERN European Organization for Nuclear Research)” January 2021 in “Asian Journal of Pharmaceutical and Clinical Research” FT-Raman spectroscopy is effective for identifying drug polymorphs, ensuring quality and stability.
July 1991 in “Endocrinology” The document contains an error.
August 2016 in “Journal of Investigative Dermatology”
67 citations
,
February 2009 in “Journal of Dermatology”
4 citations
,
January 2017 in “Journal of pediatric endocrinology & metabolism/Journal of pediatric endocrinology and metabolism” Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.
The document's conclusion cannot be provided because the content is not available.
April 2018 in “bioRxiv (Cold Spring Harbor Laboratory)” A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.
3 citations
,
January 1977 in “Archives of Dermatology” Unable to summarize document.
1 citations
,
January 1996 in “Hair transplant forum international” The document's conclusion cannot be provided because the document is not available or cannot be parsed.
7 citations
,
February 2011 in “Journal of dermatology” The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.
The document is retracted and cannot be summarized.