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    Research 961–990 of 1000+

    1. Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing Molecular Genetics & Genomic Medicine · 2025
    2. Fgf21 Deficiency Delays Hair Follicle Cycling and Modulates miRNA–Target Gene Interactions in Mice Biology · 2025
    3. Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality Journal of Investigative Dermatology · 2025
    4. P56 Azathioprine-induced alopecia totalis and knuckle hyperpigmentation in a child with uveitis: test before you leap! Rheumatology Advances in Practice · 2024
    5. 8507 Misdiagnosis of Graves’ and RAI Treatment in Patient with THRB Gene Mutation Journal of the Endocrine Society · 2024
    6. An unusual case of Anasarca-Rapunzel syndrome International Journal of Contemporary Pediatrics · 2024
    7. Spatiotemporal dynamics of sensory neuron and Merkel-cell remodeling are decoupled during epidermal homeostasis bioRxiv (Cold Spring Harbor Laboratory) · 2023
    8. Uncombable hair in a case of Zellweger syndrome – A new association Indian Dermatology Online Journal · 2023
    9. ODP408 Elevated DHEAS and Acute Hair Loss in an Adult Male with Trichorhinophalangeal Syndrome Type 1: a Case of Male PCOS Journal of the Endocrine Society · 2022
    10. Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis. 2022
    11. T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy 2022
    12. Effects of the bovine slick mutation on heat stress responses and hair growth in mice 2020
    13. P78 Acrodermatitis enteropathica in children: clinical cases 2017
    14. Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation Hormones · 2016
    15. Over-, ectopic-expression of FoxN1 at early life adversely influences lymphopoiesis (HEM3P.280) 2014
    16. How the leopard gets its spots: a transmembrane peptidase specifies feline pigmentation patterns Pigment Cell & Melanoma Research · 2013
    17. FoxN1 in K14 promoter-driven epithelium is required for generation and maintenance of 3D-thymus medulla and preventing nude phenotype in the skin (36.33) 2010
    18. Alopecia androgenética en mujeres Revista del Centro Dermatológico Pascua · 2007
    19. Does Vitamin D play a role on Msx1 homeoprotein expression involving an endogenous antisense mRNA?*1 2004
    20. The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep Agritrop (Cirad) · 2002
    21. Dissecting the bulge in hair regeneration Journal of Clinical Investigation · 2012 · 86 citations
    22. Concerted gene duplications in the two keratin gene families Journal of Molecular Evolution · 1988 · 53 citations
    23. Identification and dissection of an enhancer controlling epithelial gene expression in skin Proceedings of the National Academy of Sciences · 2001 · 29 citations
    24. Collagen-type synthesis in human-hair papilla cells in culture Archives of Dermatological Research · 1988 · 28 citations
    25. Recombinant human hair keratin proteins for halting bleeding Artificial Cells Nanomedicine and Biotechnology · 2018 · 27 citations
    26. Combinatorial Biosynthesis of Sulfated Benzenediol Lactones with a Phenolic Sulfotransferase from Fusarium graminearum PH-1 mSphere · 2020 · 22 citations
    27. Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice Cell death and disease · 2014 · 16 citations
    28. Nanoscale microenvironment engineering for expanding human hair follicle stem cell and revealing their plasticity Journal of Nanobiotechnology · 2021 · 15 citations
    29. Third International Research Workshop on Alopecia Areata Journal of Investigative Dermatology · 1999 · 15 citations
    30. Unlocking the therapeutic potential of TRPV3: Insights into thermosensation, channel modulation, and skin homeostasis involving TRPV3 BioEssays · 2024 · 10 citations