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    Research 31–60 of 56

    1. Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant Genes · 2025
    2. Genetic Hair Disorders: A Review Dermatology and Therapy · 2019 · 26 citations
    3. Diseases of Periocular Hair Survey of Ophthalmology · 2011 · 7 citations
    4. Biology and Genetics of Hair Annual Review of Genomics and Human Genetics · 2010 · 89 citations
    5. Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis Bioinformation · 2012 · 3 citations
    6. Westwood Carolina Conference on Clinical Dermatology Journal of The American Academy of Dermatology · 1983
    7. Dermatoscopy of hair shaft disorders Journal of the American Academy of Dermatology · 2012 · 68 citations
    8. Signaling Involved in Hair Follicle Morphogenesis and Development International Journal of Molecular Sciences · 2014 · 223 citations
    9. To grow or not to grow: Hair morphogenesis and human genetic hair disorders Seminars in Cell & Developmental Biology · 2013 · 43 citations
    10. Trichotillomania in Children Skin appendage disorders · 2015 · 28 citations
    11. Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants JAMA Dermatology · 2020 · 5 citations
    12. Aging and Anti-Aging in Hair and Hair Loss Elsevier eBooks · 2013 · 1 citations
    13. Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update Journal of Dermatological Science · 2012 · 52 citations
    14. Alopecia in children Clinics in Dermatology · 2000 · 7 citations
    15. Exposure to gamma-rays at the telogen phase of the hair cycle inhibits hair follicle regeneration at the anagen phase in mice International Journal of Radiation Biology · 2013 · 6 citations
    16. Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis Proceedings of the National Academy of Sciences of the United States of America · 2013 · 44 citations
    17. Frequency of Types of Alopecia in a Single-centre Hair Referral Clinic Over a Ten Years Period International Journal of Trichology · 2025
    18. Human Induced Pluripotent Stem Cell–Derived Ectodermal Precursor Cells Contribute to Hair Follicle Morphogenesis In Vivo 2013 · 64 citations
    19. CXCL12+ dermal fibroblasts promote neutrophil recruitment and host defense by recognition of IL-17 The Journal of Experimental Medicine · 2024 · 32 citations
    20. A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia Journal of Biological Research · 2019 · 11 citations
    21. Developmentally regulated expression of integrin alpha-6 distinguishes neural crest derivatives in the skin Frontiers in Cell and Developmental Biology · 2023 · 5 citations
    22. The Developmental & Molecular Requirements for Ensuring that Human Pluripotent Stem Cell-Derived Hair Follicle Bulge Stem Cells Have Acquired Competence for Hair Follicle Generation Following Transplantation Cell transplantation · 2021 · 4 citations
    23. STAT3 Partly Inhibits Cell Proliferation via Direct Negative Regulation of FST Gene Expression Frontiers in genetics · 2021 · 3 citations
    24. Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs PLoS ONE · 2024 · 2 citations
    25. Fibroblast Lineage Switching as the Developmental Origin of Scarring and Target for Regenerating Healing Preprints.org · 2026
    26. Recent Findings with Computerized Methods for Scalp Hair Growth Measurements Journal of Investigative Dermatology Symposium Proceedings · 2005 · 26 citations
    27. Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells The Journal of Dermatology · 2013 · 16 citations
    28. Trichorhinophalangeal Syndrome Dermatology · 1995 · 10 citations
    29. An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature 2018 · 10 citations
    30. New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene BMC medical genetics · 2014 · 9 citations