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    Research 961–990 of 1000+

    1. A Case of IFAP Syndrome with Severe Atopic Dermatitis Case reports in medicine · 2015 · 5 citations
    2. Alopezien und Hypotrichosen im Kindesalter Der Hautarzt · 2014 · 5 citations
    3. Single-cell analysis of temporal immune cell dynamics in alopecia areata reveals a causal role for clonally expanded CD8+ T cells in disease Cell Reports · 2025 · 4 citations
    4. GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction Journal of Investigative Dermatology · 2023 · 4 citations
    5. Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China Scientific reports · 2022 · 4 citations
    6. Marie-unna hereditary hypotrichosis International Journal of Trichology · 2014 · 4 citations
    7. Skin regional specification and higher-order <i>HoxC</i> regulation Science Advances · 2025 · 3 citations
    8. Mechanical forces across compartments coordinate cell shape and fate transitions to generate tissue architecture Nature cell biology · 2024 · 2 citations
    9. A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report Revista Paulista de Pediatria · 2024 · 2 citations
    10. Successful management of Netherton syndrome using IVIG and dupilumab: A case report Journal of Allergy and Clinical Immunology Global · 2025 · 1 citations
    11. Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies American Journal of Medical Genetics Part C Seminars in Medical Genetics · 2025 · 1 citations
    12. Single-Cell Transcriptome Sequence Profiling on the Morphogenesis of Secondary Hair Follicles in Ordos Fine-Wool Sheep International journal of molecular sciences · 2024 · 1 citations
    13. Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports Journal of neuroendocrinology · 2023 · 1 citations
    14. DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma Frontiers in Cardiovascular Medicine · 2023 · 1 citations
    15. Diseases of the Canine Prostate Gland Veterinary medicine and science · 2022 · 1 citations
    16. A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome Annals of Dermatology · 2022 · 1 citations
    17. Acne Syndromes and Mosaicism Biomedicines · 2021 · 1 citations
    18. Antioxidant and Antiproliferative Activity of Finasteride against Glioblastoma Cells Pharmaceutics · 2021 · 1 citations
    19. Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors Journal of Investigative Dermatology · 2026
    20. IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep Small Ruminant Research · 2026
    21. Who Am I? Eyebrow Follicles Minimize Donor-Derived DNA for Germline Testing After Hematopoietic Stem Cell Transplantation International Journal of Molecular Sciences · 2026
    22. In vitro cultured human-derived HFMSCs have shown the potential to promote wound China National GeneBank DataBase · 2026
    23. Multi-omics analysis unveils the role of cancer-associated fibroblasts in cutaneous squamous cell carcinoma Cancer Cell International · 2025
    24. Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock BMC Pediatrics · 2025
    25. The Effects of Spermidine on Functional and Transcriptomic Markers in Human Primary Keratinocytes Physiologia · 2025
    26. Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review Frontiers in Medicine · 2025
    27. Dietary and Genetic Aspects of Polycystic Ovary Syndrome (PCOS) in Polish Women-Part II: Association of PubMed · 2025
    28. Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree Frontiers in Genetics · 2025
    29. Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement Genes · 2024
    30. EBS in Children with De Novo Pathogenic Variants Disturbing Krt14 International journal of molecular sciences · 2024