Search
for

    Sort by

    Research 421–450 of 1000+

    1. FGF Family: From Drug Development to Clinical Application International Journal of Molecular Sciences · 2018 · 103 citations
    2. An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis Journal of Investigative Dermatology · 2006 · 97 citations
    3. PROTACs: A novel strategy for cancer drug discovery and development MedComm · 2023 · 44 citations
    4. Epidermal Differentiation Complex: A Review on Its Epigenetic Regulation and Potential Drug Targets. PubMed · 2016 · 39 citations
    5. A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue Journal of Investigative Dermatology · 2004 · 31 citations
    6. A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia Journal of Investigative Dermatology · 2002 · 26 citations
    7. The Genetic Architecture of Alopecia Areata Journal of Investigative Dermatology Symposium Proceedings · 2013 · 23 citations
    8. Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease Cell Reports · 2022 · 14 citations
    9. Multiomics global landscape of stemness-related gene clusters in adipose-derived mesenchymal stem cells Stem Cell Research & Therapy · 2020 · 13 citations
    10. Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak Frontiers in Genetics · 2022 · 7 citations
    11. Cellular Senescence and Aging in Myotonic Dystrophy International Journal of Molecular Sciences · 2022 · 4 citations
    12. Vitamin D Receptor gene polymorphisms taq-1 and cdx-1 in female pattern hair loss Indian Journal of Dermatology · 2020 · 3 citations
    13. Isochromosome Mosaic Turner Syndrome: A Case Report Journal of the ASEAN Federation of Endocrine Societies · 2019 · 3 citations
    14. Conjoint analysis of methylation, transcriptomic, and proteomic profiles in pemphigus vulgaris Orphanet Journal of Rare Diseases · 2024 · 1 citations
    15. The Multiple Consequences of Obesity IntechOpen eBooks · 2022 · 1 citations
    16. Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023 Irish Journal of Medical Science (1971 -) · 2024
    17. Association between PITX2 polymorphism and androgenetic alopecia in the Indian population Indian Journal of Dermatology Venereology and Leprology · 2024
    18. E-Poster Indian Journal of Endocrinology and Metabolism · 2023
    19. Bioinformatic analysis of gene expression data reveals Src family protein tyrosine kinases as key players in androgenetic alopecia Frontiers in Medicine · 2023
    20. Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism AACE clinical case reports · 2021
    21. Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development Biology Direct · 2016 · 19 citations
    22. Phytochemistry, pharmacological activity, and potential health benefits of Glycyrrhiza glabra Heliyon · 2021 · 119 citations
    23. Matrix Metalloproteinase-19 Expression in Normal and Diseased Skin: Dysregulation by Epidermal Proliferation Journal of Investigative Dermatology · 2003 · 56 citations
    24. Development, Structure, and Keratin Expression in <i>C57BL/6J</i> Mouse Eccrine Glands Veterinary pathology · 2011 · 29 citations
    25. Abstracts from the 4th Annual Student Medical Summit BMC Proceedings · 2021 · 1 citations
    26. Ichthyosis American journal of clinical dermatology · 2003 · 147 citations
    27. Hormonal Therapies for Individuals with Intersex Conditions Treatments in Endocrinology · 2005 · 48 citations
    28. Synopsis: 2005 Annual Meeting of the American Society of Andrology Journal of Andrology · 2005 · 1 citations
    29. Tracking the Path of the Original: A Forensic Genetic, Demographic, and Legal Audit of the Muur Continuity Hypothesis Zenodo (CERN European Organization for Nuclear Research) · 2026
    30. Tracking the Path of the Original: A Forensic Genetic, Demographic, and Legal Audit of the Muur Continuity Hypothesis Zenodo (CERN European Organization for Nuclear Research) · 2026