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    Research 901–930 of 1000+

    1. PNKP is required for maintaining the integrity of progenitor cell populations in adult mice Life science alliance · 2021 · 3 citations
    2. Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient Molecular genetics & genomic medicine · 2021 · 3 citations
    3. Novel Mutation in the Hemojuvelin Gene (HJV) in a Patient with Juvenile Hemochromatosis Presenting with Insulin-dependent Diabetes Mellitus, Secondary Hypothyroidism and Hypogonadism American Journal of Case Reports · 2020 · 3 citations
    4. Epstein-Barr virus associated with high-grade B-cell lymphoma in nude severe combined immunodeficiency BMJ case reports · 2019 · 3 citations
    5. Pyruvate Kinase M2 Role in Cardiovascular Repair Cells · 2025 · 2 citations
    6. Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia JCEM Case Reports · 2024 · 2 citations
    7. Differential transcriptome study on the damage of testicular tissues caused by chronic infection of T. gondii in mice Parasites & Vectors · 2024 · 2 citations
    8. A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report Revista Paulista de Pediatria · 2024 · 2 citations
    9. Autophagy critically controls skin inflammation and apoptosis-induced stem cell activation Autophagy · 2023 · 2 citations
    10. Characters of KRT80 and its roles in neoplasms diseases Cancer medicine · 2023 · 2 citations
    11. Genome wide association analysis of root hair traits in rice reveals novel genomic regions controlling epidermal cell differentiation BMC plant biology · 2023 · 2 citations
    12. Construction and functional analysis of ceRNA regulatory network related to the development of secondary hair follicles in Inner Mongolia cashmere goats Frontiers in Veterinary Science · 2022 · 2 citations
    13. Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome The Application of Clinical Genetics · 2022 · 2 citations
    14. Identification of llama KRTAP7-1 and KRTAP8-1 fiber genes and polymorphism screening Small ruminant research · 2019 · 2 citations
    15. RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS 2017 · 2 citations
    16. Anabolic and Metabolic Effects of Testosterone and Other Androgens: Direct Effects and Role of Testosterone Metabolic Products Endocrinology · 2017 · 2 citations
    17. Structural and epistatic regulatory variants cause hallmark white spotting in cattle Science Advances · 2025 · 1 citations
    18. Identification of lncRNAs involved in the hair follicle cycle transition of cashmere goats in response to photoperiod change BMC Genomics · 2025 · 1 citations
    19. Investigating the Genetic Association of Selected Candidate Loci with Alopecia Areata Susceptibility in Jordanian Patients Medicina · 2025 · 1 citations
    20. Alterations in Methionine Cycle and Wnt/MAPK Signaling Associated with HMBi-Induced Cashmere Growth in Goats International Journal of Molecular Sciences · 2025 · 1 citations
    21. Conjoint analysis of methylation, transcriptomic, and proteomic profiles in pemphigus vulgaris Orphanet Journal of Rare Diseases · 2024 · 1 citations
    22. Adult Male Hypogonadism: A Laboratory Medicine Perspective on Its Diagnosis and Management Diagnostics · 2023 · 1 citations
    23. Food Administration and Not Genetic Variants Causes Pharmacokinetic Variability of Tadalafil and Finasteride Journal of personalized medicine · 2023 · 1 citations
    24. Inheritance-Specific Dysregulation of Th1- and Th17-Associated Cytokines in Alopecia Areata Biomolecules · 2023 · 1 citations
    25. Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep Journal of Animal Science and Biotechnology · 2023 · 1 citations
    26. Vitamin D receptor cross-talk with p63 signaling promotes epidermal cell fate 2023 · 1 citations
    27. Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters European Journal of Human Genetics · 2023 · 1 citations
    28. Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose BMC Genomics · 2022 · 1 citations
    29. Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year JCRPE · 2022 · 1 citations
    30. Androgens/Androgen Receptor in the Management of Skin Diseases Journal of Biosciences and Medicines · 2022 · 1 citations