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    Research 181–210 of 764

    1. Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese PLoS ONE · 2015 · 10 citations
    2. Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review The Journal of Dermatology · 2018 · 9 citations
    3. Untersuchungen der Fremdstoffbindung in permanenten Keratinozyten- und Melanozyten-Zelllinien sowie die Eignung von Primärkulturen aus humanen Haarfollikeln zur In-vitro-Messung der Fremdstoffaufnahme im Haar Carl von Ossiezky University of Oldenburg · 2006
    4. Expression of epidermal keratins and filaggrin during human fetal skin development. The Journal of Cell Biology · 1985 · 292 citations
    5. SOCS1 and SOCS3 as key checkpoint molecules in the immune responses associated to skin inflammation and malignant transformation Frontiers in Immunology · 2024 · 26 citations
    6. Venus trap in the mouse embryo reveals distinct molecular dynamics underlying specification of first embryonic lineages EMBO Reports · 2015 · 25 citations
    7. “Structural imprinting” of the cutaneous immune effector function Tissue Barriers · 2020 · 4 citations
    8. One Transgene: Two Outcomes Science s STKE · 2002
    9. Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation The Journal of Cell Biology · 2001 · 195 citations
    10. Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2 2022 · 8 citations
    11. An LRH-RSL4 feedback regulatory loop controls the determinate growth of root hairs in Arabidopsis Current Biology · 2023 · 5 citations
    12. Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin Frontiers in Physiology · 2021 · 18 citations
    13. CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep ˜The œFEBS journal · 2017 · 47 citations
    14. XIAP Stabilizes DDRGK1 to Promote ER‐Phagy and Protects Against Noise‐Induced Hearing Loss Advanced Science · 2026
    15. The developmental basis of fingerprint pattern formation and variation Cell · 2023 · 44 citations
    16. Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment Cells · 2019 · 39 citations
    17. Strategies for High-Efficiency Mutation Using the CRISPR/Cas System Frontiers in Cell and Developmental Biology · 2022 · 29 citations
    18. Premature aging syndromes: From patients to mechanism Journal of dermatological science · 2019 · 29 citations
    19. Genetically modified laboratory mice with sebaceous glands abnormalities Cellular and Molecular Life Sciences · 2016 · 22 citations
    20. Endoplasmic reticulum in health and disease: the 12th International Calreticulin Workshop, Delphi, Greece Journal of Cellular and Molecular Medicine · 2017 · 13 citations
    21. The heme-responsive PrrH sRNA regulates <i>Pseudomonas aeruginosa</i> pyochelin gene expression mSphere · 2023 · 11 citations
    22. Role of the Wnt signaling pathway in keratoacanthoma Cancer reports · 2019 · 2 citations
    23. Controlling Hair Loss by Regulating Apoptosis in Hair Follicles: A Comprehensive Overview Biomolecules · 2023 · 1 citations
    24. Antiandrogenic activity of Riboflavin 5′-phosphate (FMN) in 22Rv1 and LNCaP human prostate cancer cell lines European Journal of Pharmacology · 2022 · 1 citations
    25. Recombinant Goat VEGF164 Increases Hair Growth by Painting Process on the Skin of Shaved Mouse Asian-Australasian Journal of Animal Sciences · 2014 · 1 citations
    26. A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome American journal of medical genetics. Part A · 2023
    27. Independent DSG4 frameshift variants in cats with hair shaft dystrophy Molecular genetics and genomics · 2021
    28. On the Role of Melatonin in Skin Physiology and Pathology Endocrine journal · 2005 · 222 citations
    29. Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia The American Journal of Human Genetics · 2012 · 74 citations
    30. Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families Molecular genetics & genomic medicine · 2022 · 5 citations