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    Research 421–450 of 605

    1. 547 CDK9 Kinase Activation in Association with AFF1-SEC Initiate Epidermal Progenitor differentiation Journal of Investigative Dermatology · 2022
    2. Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism Authorea (Authorea) · 2022
    3. G338(P) Dermatological manifestations in children with chronic kidney disease in a tertiary care center: a case-control study 2020
    4. SUN-287 A Case of Ectopic Neurohypophysis Journal of the Endocrine Society · 2020
    5. Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients 2018
    6. Escobar syndrome (multiple pterygium syndrome) associated with osteogenesis imperfecta: a case report ORTHOPAEDICS TRAUMATOLOGY and PROSTHETICS · 2017
    7. Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development 2017
    8. Early Onset Werner Syndrome Turkish Journal of Endocrinology and Metabolism · 2015
    9. Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities Neuropediatrics · 2012
    10. This Month in the Journal The American Journal of Human Genetics · 2005
    11. Propecia-induced spermatogenic failure: a report of two cases Fertility and Sterility · 2007 · 49 citations
    12. The Current and Emerging Role of Statins in the Treatment of PCOS: The Evidence to Date Medicina · 2024
    13. Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice Journal of Biological Chemistry · 2002 · 15 citations
    14. Metabolic Regulation of Hematopoietic Stem Cells in the Hypoxic Niche Cell stem cell · 2011 · 695 citations
    15. Fibroblasts: Origins, definitions, and functions in health and disease Cell · 2021 · 488 citations
    16. Vitamin D: More Than a “Bone-a-Fide” Hormone Molecular endocrinology · 2003 · 276 citations
    17. SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder Cell · 2010 · 260 citations
    18. Dermal β-catenin activity in response to epidermal Wnt ligands is required for fibroblast proliferation and hair follicle initiation Development · 2012 · 207 citations
    19. A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy Molecular cell · 1998 · 188 citations
    20. Lack of the Vitamin D Receptor is Associated with Reduced Epidermal Differentiation and Hair Follicle Growth 2002 · 180 citations
    21. An Integrated Transcriptome Atlas of Embryonic Hair Follicle Progenitors, Their Niche, and the Developing Skin Developmental cell · 2015 · 173 citations
    22. Cantú Syndrome Is Caused by Mutations in ABCC9 The American Journal of Human Genetics · 2012 · 148 citations
    23. Basal cell carcinoma — molecular biology and potential new therapies Journal of Clinical Investigation · 2012 · 146 citations
    24. WNT Signaling in Disease Cells · 2019 · 144 citations
    25. British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology British Journal of Dermatology · 2010 · 136 citations
    26. Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat (Capra hircus) BMC Genomics · 2017 · 129 citations
    27. Type XVII collagen coordinates proliferation in the interfollicular epidermis eLife · 2017 · 124 citations
    28. Dermal fibroblast in cutaneous development and healing Wiley Interdisciplinary Reviews-Developmental Biology · 2017 · 115 citations
    29. RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome The American Journal of Human Genetics · 2012 · 112 citations
    30. Extrapulmonary disorders associated with Rhodococcus equi infection in foals: 150 cases (1987–2007) Javma-journal of The American Veterinary Medical Association · 2009 · 108 citations